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<h1><a data-section="Header" data-ga-action="Click-on"
data-ga-label="dbSNP Short Genetic Variations"
ref="section=Header&action=Click-on&label=dbSNP Short Genetic Variations"
href="/snp/">dbSNP</a>
<span class="uswds-gray tagline">Short Genetic Variations</span>
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<h3 class="usa-alert-heading">Welcome to the Reference SNP (rs) Report</h3>
<p class="usa-alert-text">All alleles are reported in the <a href="https://www.ncbi.nlm.nih.gov/core/assets/snp/docs/RefSNP_orientation_updates.pdf" target="_blank"
data-ga-action="Click for forward orientation" data-ga-category="Info panel"
data-ga-label="Forward orientation">Forward orientation</a>. Click on the
<a href="#variant_details" id="variantlink"
data-ga-action="Click for variant details" data-ga-category="Info panel"
data-ga-label="Forward orientation">Variant Details tab</a> for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the
<a href="#hgvs_tab" id="hgvslink"
data-ga-action="Click for aliases tab" data-ga-category="Info panel"
data-ga-label="HGVS tab">HGVS tab</a>.</p>
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<h3>Reference SNP (rs) Report</h3>
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<ul class="utilities usa-unstyled-list align-right">
<li title="Download in API JSON format"><a href="https://api.ncbi.nlm.nih.gov/variation/v0/refsnp/1057910"
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<p id="main_tp">
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.<br/>
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.<br/>
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors. <br/>
For more information see <a class="external-link" href="/snp/docs/refsnp_report/helpdoc"> Help documentation</a>.</p>
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<h2 id="refsnp_id">rs1057910</h2>
</div>
</div>
<div class="accession usa-width-one-third">
<p>Current Build <span>157</span></p>
<p>Released <span>
September 3, 2024
</span></p>
</div>
</div>
<div class="summary-box usa-grid-full">
<dl class="usa-width-one-half">
<dt>Organism</dt>
<dd class="species_name">Homo sapiens</dd>
<dt>Position</dt>
<dd>
<span>chr10:94981296 </span><span>(GRCh38.p14) </span><a data-width="640px" href="#pos_tp"
ref="section=Summary&action=Click-on-Tooltip&label=pos_tp"
data-section="Summary" data-ga-action="Click-on-Tooltip"
data-ga-label="pos_tp" class="fa fa-question-circle ncbiPopper" id="position_tooltip"><span class="usa-sr-only">Help</span></a><p id="pos_tp">The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See <a href="/snp/docs/refsnp_report/helpdoc/">here</a> for details.</p>
</dd>
<dt>Alleles</dt>
<dd>
A>C / A>G
</dd>
<dt>Variation Type</dt>
<dd>
SNV
<span class="small-font gray">Single Nucleotide Variation</span>
</dd>
<dt>Frequency</dt>
<dd>
<div>
C=0.063889
(20338/318334, ALFA)
</div><div>
C=0.063706
(7725/121260, ExAC)
</div><span>
C=0.02453 (1900/77444, 38KJPN)
</span><span>(<a id="expandfrequency" data-freq-remn="22"
data-is-icon="false" data-section="Summary" data-ga-action="Click-on"
data-ga-label="Frequency" data-targets="#remn_summ_freq" href="#remn_summ_freq"
ref="section=Summary&action=Click-on&label=Frequency">+ 22 more</a>)</span><div class="ui-widget hide_elm" id="remn_summ_freq"><div>
C=0.0449
(325/7232, Korea4K)
</div><div>
C=0.0458
(293/6404, 1000G_30X)
</div><div>
C=0.0485
(243/5008, 1000G)
</div><div>
C=0.0732
(328/4480, Estonian)
</div><div>
C=0.0633
(244/3854, ALSPAC)
</div><div>
C=0.0612
(227/3708, TWINSUK)
</div><div>
C=0.0413
(121/2930, KOREAN)
</div><div>
C=0.0524
(132/2520, PharmGKB)
</div><div>
C=0.0566
(118/2084, HGDP_Stanford)
</div><div>
C=0.0459
(84/1832, Korea1K)
</div><div>
C=0.0545
(72/1320, HapMap)
</div><div>
C=0.1288
(145/1126, Daghestan)
</div><div>
C=0.069
(69/998, GoNL)
</div><div>
C=0.051
(39/764, PRJEB37584)
</div><div>
C=0.029
(18/614, Vietnamese)
</div><div>
C=0.085
(51/600, NorthernSweden)
</div><div>
C=0.077
(41/534, MGP)
</div><div>
C=0.066
(20/302, FINRISK)
</div><div>
C=0.019
(4/216, Qatari)
</div><div>
A=0.47
(38/80, SGDP_PRJ)
</div><div>
C=0.05
(4/74, Ancient Sardinia)
</div><div>
A=0.42
(5/12, Siberian)
</div></div>
</dd>
</dl>
<dl class="usa-width-one-half">
<dt>Clinical Significance</dt>
<dd>
Reported in <a target="_blank" data-section="Summary" data-ga-action="Click-on"
data-ga-label="Reported in ClinVar"
ref="section=Summary&action=Click-on&label=Reported in ClinVar"
href="/clinvar?term=((175053[AlleleID])OR(23447[AlleleID]))">ClinVar</a>
</dd>
<dt>Gene : Consequence</dt>
<dd>
<span>CYP2C9 : Missense Variant</span>
</dd>
<dt>Publications</dt>
<dd>
<a id="snp_pub_count" href="#publications">305
citations
</a>
</dd>
<dt>Genomic View</dt>
<dd>
<a href="#seq_hash" data-section="Summary" data-ga-action="Click-on"
data-ga-label="Genomic View See rs on genome"
ref="section=Summary&action=Click-on&label=Genomic View See rs on genome">See rs on
genome</a>
</dd>
</dl>
</div>
<div class="js-tabs">
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<li class="js-tablist__item">
<a href="#frequency_tab" ref="section=Tab&action=Click-on&label=Frequency"
data-ga-action="Click-on-horizontal" data-ga-label="Frequency" id="label_id_third"
class="js-tablist__link">Frequency
<span aria-hidden="true"></span></a>
</li>
<li class="js-tablist__item">
<a href="#variant_details" ref="section=Tab&action=Click-on&label=Variant Details"
data-ga-action="Click-on-horizontal" data-ga-label="Variant Details" id="label_id_first"
class="js-tablist__link">Variant Details
<span class="js-tablist__item-has-focus" aria-hidden="true"></span></a>
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ref="section=Tab&action=Click-on&label=Clinical Significance"
data-ga-action="Click-on-horizontal" data-ga-label="Clinical Significance" id="label_id_second"
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Significance
<span aria-hidden="true"></span></a>
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<a href="#hgvs_tab" ref="section=Tab&action=Click-on&label=HGVS"
data-ga-action="Click-on-horizontal" data-ga-label="HGVS" id="label_id_fourth"
class="js-tablist__link">HGVS
<span aria-hidden="true"></span></a>
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<a href="#submissions" ref="section=Tab&action=Click-on&label=Submissions"
data-ga-action="Click-on-horizontal" data-ga-label="Submissions" id="label_id_fifth"
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data-ga-action="Click-on-horizontal" data-ga-label="Publications" id="label_id_seventh"
class="js-tablist__link">Publications
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data-ga-action="Click-on-horizontal" data-ga-label="Flanks" id="label_id_eighth"
class="js-tablist__link">Flanks
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ref="section=Frequency&action=Click-on-Popper&label=popfreq_tp"
data-section="Frequency" data-ga-action="Click-on-Popper"
data-ga-label="popfreq_tp" >
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<p id="popfreq_tp">
<font size="5" color="blue"><strong><a href="/snp/docs/gsr/alfa" rel="nofollow" target="_blank">ALFA Allele Frequency</a></strong></font><br/>
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project <a href="/snp/docs/gsr/alfa" rel="nofollow" target="_blank">page</a> including descriptions, data access, and terms of use.
</p>
<div>
<span class="build_id_container"><span class="build_id_label">Release Version:</span>&nbsp;20231103111315</span>
</div>
<div id="popfreq_table" data-section="PopFrequency" data-ga-action="ScrollPopFrequency" data-ga-label="popfreq" class="popfreq_table">
<table id="popfreq_datatable" class="stripe">
<thead>
<tr>
<th title="Continental population name">Population</th>
<th title="Global (total) and sub-populations">Group</th>
<th title="Total allele counts by population">Sample Size</th>
<th title="Reference assembly allele">Ref Allele</th>
<th title="Alternate allele">Alt Allele</th>
<th title="Reference Homozygous genotype Frequency">Ref HMOZ</th>
<th title="Alternate Homozygous genotype Frequency">Alt HMOZ</th>
<th title="Heterozygous genotype Frequency">HTRZ</th>
<th title="-Log(HWE Probability)">HWEP</th>
</tr>
</thead>
<tbody>
<tr class="par_row">
<td>
<a href="/biosample/SAMN10492705">Total</a>
</td>
<td>Global</td>
<td class="samp_s">318334</td>
<td class="popfreq_ref_allele">A=0.936111</td>
<td class="popfreq_alt_allele">C=0.063889, G=0.000000</td>
<td class="popfreq_alt_allele">0.876815</td>
<td class="popfreq_alt_allele">0.004593</td>
<td class="popfreq_alt_allele">0.118592</td>
<td class="popfreq_alt_allele">7</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492695">European</a>
</td>
<td>Sub</td>
<td class="samp_s">265006</td>
<td class="popfreq_ref_allele">A=0.933345</td>
<td class="popfreq_alt_allele">C=0.066655, G=0.000000</td>
<td class="popfreq_alt_allele">0.871354</td>
<td class="popfreq_alt_allele">0.004664</td>
<td class="popfreq_alt_allele">0.123982</td>
<td class="popfreq_alt_allele">1</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492703">African</a>
</td>
<td>Sub</td>
<td class="samp_s">14506</td>
<td class="popfreq_ref_allele">A=0.98773</td>
<td class="popfreq_alt_allele">C=0.01227, G=0.00000</td>
<td class="popfreq_alt_allele">0.975734</td>
<td class="popfreq_alt_allele">0.000276</td>
<td class="popfreq_alt_allele">0.02399</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492696">African Others</a>
</td>
<td>Sub</td>
<td class="samp_s">518</td>
<td class="popfreq_ref_allele">A=0.998</td>
<td class="popfreq_alt_allele">C=0.002, G=0.000</td>
<td class="popfreq_alt_allele">0.996139</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.003861</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492698">African American</a>
</td>
<td>Sub</td>
<td class="samp_s">13988</td>
<td class="popfreq_ref_allele">A=0.98735</td>
<td class="popfreq_alt_allele">C=0.01265, G=0.00000</td>
<td class="popfreq_alt_allele">0.974979</td>
<td class="popfreq_alt_allele">0.000286</td>
<td class="popfreq_alt_allele">0.024735</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492704">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">6754</td>
<td class="popfreq_ref_allele">A=0.9550</td>
<td class="popfreq_alt_allele">C=0.0450, G=0.0000</td>
<td class="popfreq_alt_allele">0.911756</td>
<td class="popfreq_alt_allele">0.001777</td>
<td class="popfreq_alt_allele">0.086467</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492697">East Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">4858</td>
<td class="popfreq_ref_allele">A=0.9564</td>
<td class="popfreq_alt_allele">C=0.0436, G=0.0000</td>
<td class="popfreq_alt_allele">0.914368</td>
<td class="popfreq_alt_allele">0.001647</td>
<td class="popfreq_alt_allele">0.083985</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492701">Other Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">1896</td>
<td class="popfreq_ref_allele">A=0.9515</td>
<td class="popfreq_alt_allele">C=0.0485, G=0.0000</td>
<td class="popfreq_alt_allele">0.905063</td>
<td class="popfreq_alt_allele">0.00211</td>
<td class="popfreq_alt_allele">0.092827</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492699">Latin American 1</a>
</td>
<td>Sub</td>
<td class="samp_s">1000</td>
<td class="popfreq_ref_allele">A=0.940</td>
<td class="popfreq_alt_allele">C=0.060, G=0.000</td>
<td class="popfreq_alt_allele">0.884</td>
<td class="popfreq_alt_allele">0.004</td>
<td class="popfreq_alt_allele">0.112</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492700">Latin American 2</a>
</td>
<td>Sub</td>
<td class="samp_s">5806</td>
<td class="popfreq_ref_allele">A=0.9607</td>
<td class="popfreq_alt_allele">C=0.0393, G=0.0000</td>
<td class="popfreq_alt_allele">0.92215</td>
<td class="popfreq_alt_allele">0.000689</td>
<td class="popfreq_alt_allele">0.077162</td>
<td class="popfreq_alt_allele">1</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492702">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">5136</td>
<td class="popfreq_ref_allele">A=0.8853</td>
<td class="popfreq_alt_allele">C=0.1147, G=0.0000</td>
<td class="popfreq_alt_allele">0.788162</td>
<td class="popfreq_alt_allele">0.017523</td>
<td class="popfreq_alt_allele">0.194315</td>
<td class="popfreq_alt_allele">3</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN11605645">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">20126</td>
<td class="popfreq_ref_allele">A=0.93466</td>
<td class="popfreq_alt_allele">C=0.06534, G=0.00000</td>
<td class="popfreq_alt_allele">0.874888</td>
<td class="popfreq_alt_allele">0.005565</td>
<td class="popfreq_alt_allele">0.119547</td>
<td class="popfreq_alt_allele">3</td>
</tr>
</tbody>
</table>
<br/>
<br/>
</div>
<a data-width="640px" href="#frequency_tp"
ref="section=Frequency&action=Click-on-Tooltip&label=frequency_tp"
data-section="Frequency" data-ga-action="Click-on-Tooltip"
data-ga-label="frequency_tp" class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="frequency_tp">
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
</p>
<a href="/snp/rs1057910/download/frequency">
<i class="fa fa-download" aria-hidden="true"></i> Download</a>
<div id="dbsnp_freq_table">
<table id="dbsnp_freq_datatable" class="stripe">
<thead>
<tr>
<th class="study_header">Study</th>
<th class="population_header">Population</th>
<th>Group</th>
<th>Sample Size</th>
<th>Ref Allele</th>
<th>Alt Allele</th>
</tr>
</thead>
<tbody>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492705">Total</a>
</td>
<td>Global</td>
<td class="samp_s">318334</td>
<td>A=0.936111</td>
<td>C=0.063889, G=0.000000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492695">European</a>
</td>
<td>Sub</td>
<td class="samp_s">265006</td>
<td>A=0.933345</td>
<td>C=0.066655, G=0.000000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN11605645">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">20126</td>
<td>A=0.93466</td>
<td>C=0.06534, G=0.00000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492703">African</a>
</td>
<td>Sub</td>
<td class="samp_s">14506</td>
<td>A=0.98773</td>
<td>C=0.01227, G=0.00000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492704">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">6754</td>
<td>A=0.9550</td>
<td>C=0.0450, G=0.0000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492700">Latin American 2</a>
</td>
<td>Sub</td>
<td class="samp_s">5806</td>
<td>A=0.9607</td>
<td>C=0.0393, G=0.0000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492702">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">5136</td>
<td>A=0.8853</td>
<td>C=0.1147, G=0.0000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
</td>
<td>
<a href="/biosample/SAMN10492699">Latin American 1</a>
</td>
<td>Sub</td>
<td class="samp_s">1000</td>
<td>A=0.940</td>
<td>C=0.060, G=0.000</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
<a href="/biosample/SAMN07490465">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">121260</td>
<td>A=0.936294</td>
<td>C=0.063706</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
Europe
</td>
<td>Sub</td>
<td class="samp_s">73314</td>
<td>A=0.93230</td>
<td>C=0.06770</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
Asian
</td>
<td>Sub</td>
<td class="samp_s">25154</td>
<td>A=0.91413</td>
<td>C=0.08587</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">11480</td>
<td>A=0.96420</td>
<td>C=0.03580</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">10404</td>
<td>A=0.98741</td>
<td>C=0.01259</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
<a href="/biosample/SAMN07486028">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">908</td>
<td>A=0.934</td>
<td>C=0.066</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA678214">38KJPN</a>
</td>
<td>
<a href="/biosample/SAMN33574975">JAPANESE</a>
</td>
<td>Study-wide</td>
<td class="samp_s">77444</td>
<td>A=0.97547</td>
<td>C=0.02453</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA974196">Korean Genome Project 4K</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">7232</td>
<td>A=0.9551</td>
<td>C=0.0449</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07490465">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">6404</td>
<td>A=0.9542</td>
<td>C=0.0458</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07486022">African</a>
</td>
<td>Sub</td>
<td class="samp_s">1786</td>
<td>A=0.9983</td>
<td>C=0.0017</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07488239">Europe</a>
</td>
<td>Sub</td>
<td class="samp_s">1266</td>
<td>A=0.9313</td>
<td>C=0.0687</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07486027">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">1202</td>
<td>A=0.8985</td>
<td>C=0.1015</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07486024">East Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">1170</td>
<td>A=0.9650</td>
<td>C=0.0350</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB31736">1000Genomes_30X</a>
</td>
<td>
<a href="/biosample/SAMN07488242">American</a>
</td>
<td>Sub</td>
<td class="samp_s">980</td>
<td>A=0.959</td>
<td>C=0.041</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07490465">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">5008</td>
<td>A=0.9515</td>
<td>C=0.0485</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07486022">African</a>
</td>
<td>Sub</td>
<td class="samp_s">1322</td>
<td>A=0.9977</td>
<td>C=0.0023</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07486024">East Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">1008</td>
<td>A=0.9663</td>
<td>C=0.0337</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07488239">Europe</a>
</td>
<td>Sub</td>
<td class="samp_s">1006</td>
<td>A=0.9274</td>
<td>C=0.0726</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07486027">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">978</td>
<td>A=0.891</td>
<td>C=0.109</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6930">1000Genomes</a>
</td>
<td>
<a href="/biosample/SAMN07488242">American</a>
</td>
<td>Sub</td>
<td class="samp_s">694</td>
<td>A=0.963</td>
<td>C=0.037</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA489787">Genetic variation in the Estonian population</a>
</td>
<td>
Estonian
</td>
<td>Study-wide</td>
<td class="samp_s">4480</td>
<td>A=0.9268</td>
<td>C=0.0732</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7217">The Avon Longitudinal Study of Parents and Children</a>
</td>
<td>
PARENT AND CHILD COHORT
</td>
<td>Study-wide</td>
<td class="samp_s">3854</td>
<td>A=0.9367</td>
<td>C=0.0633</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7218">UK 10K study - Twins</a>
</td>
<td>
TWIN COHORT
</td>
<td>Study-wide</td>
<td class="samp_s">3708</td>
<td>A=0.9388</td>
<td>C=0.0612</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA589833">KOREAN population from KRGDB</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">2930</td>
<td>A=0.9587</td>
<td>C=0.0413</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13103781">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">2520</td>
<td>A=0.9476</td>
<td>C=0.0524</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13102994">PA152211301</a>
</td>
<td>Sub</td>
<td class="samp_s">696</td>
<td>A=0.953</td>
<td>C=0.047</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13103498">PA154394460</a>
</td>
<td>Sub</td>
<td class="samp_s">584</td>
<td>A=0.938</td>
<td>C=0.062</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13094147">PA130478249</a>
</td>
<td>Sub</td>
<td class="samp_s">464</td>
<td>A=0.966</td>
<td>C=0.034</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13100665">PA149566605</a>
</td>
<td>Sub</td>
<td class="samp_s">356</td>
<td>A=0.952</td>
<td>C=0.048</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13102992">PA152209538</a>
</td>
<td>Sub</td>
<td class="samp_s">184</td>
<td>A=0.918</td>
<td>C=0.082</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13094120">PA130443285</a>
</td>
<td>Sub</td>
<td class="samp_s">158</td>
<td>A=0.924</td>
<td>C=0.076</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13094151">PA130491144</a>
</td>
<td>Sub</td>
<td class="samp_s">58</td>
<td>A=0.98</td>
<td>C=0.02</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13094153">PA130491273</a>
</td>
<td>Sub</td>
<td class="samp_s">20</td>
<td>A=0.90</td>
<td>C=0.10</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">2084</td>
<td>A=0.9434</td>
<td>C=0.0566</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169023">Est_Asia</a>
</td>
<td>Sub</td>
<td class="samp_s">470</td>
<td>A=0.955</td>
<td>C=0.045</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169022">Central_South_Asia</a>
</td>
<td>Sub</td>
<td class="samp_s">414</td>
<td>A=0.903</td>
<td>C=0.097</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169025">Middle_Est</a>
</td>
<td>Sub</td>
<td class="samp_s">350</td>
<td>A=0.934</td>
<td>C=0.066</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169024">Europe</a>
</td>
<td>Sub</td>
<td class="samp_s">320</td>
<td>A=0.916</td>
<td>C=0.084</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169020">Africa</a>
</td>
<td>Sub</td>
<td class="samp_s">242</td>
<td>A=1.000</td>
<td>C=0.000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169021">America</a>
</td>
<td>Sub</td>
<td class="samp_s">216</td>
<td>A=0.986</td>
<td>C=0.014</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB6463">HGDP-CEPH-db Supplement 1</a>
</td>
<td>
<a href="/biosample/SAMN13169026">Oceania</a>
</td>
<td>Sub</td>
<td class="samp_s">72</td>
<td>A=0.94</td>
<td>C=0.06</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA609628">Korean Genome Project</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">1832</td>
<td>A=0.9541</td>
<td>C=0.0459</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA60817">HapMap</a>
</td>
<td>
<a href="/biosample/SAMN10820145">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">1320</td>
<td>A=0.9455</td>
<td>C=0.0545</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">HapMap</a>
</td>
<td>
<a href="/biosample/SAMN10821182">American</a>
</td>
<td>Sub</td>
<td class="samp_s">770</td>
<td>A=0.932</td>
<td>C=0.068</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">HapMap</a>
</td>
<td>
<a href="/biosample/SAMN10821184">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">254</td>
<td>A=0.965</td>
<td>C=0.035</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">HapMap</a>
</td>
<td>
<a href="/biosample/SAMN10821183">Europe</a>
</td>
<td>Sub</td>
<td class="samp_s">176</td>
<td>A=0.938</td>
<td>C=0.062</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">HapMap</a>
</td>
<td>
<a href="/biosample/SAMN10821181">African</a>
</td>
<td>Sub</td>
<td class="samp_s">120</td>
<td>A=1.000</td>
<td>C=0.000</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013121">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">1126</td>
<td>A=0.8712</td>
<td>C=0.1288</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013126">Daghestan</a>
</td>
<td>Sub</td>
<td class="samp_s">624</td>
<td>A=0.827</td>
<td>C=0.173</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013123">Near_East</a>
</td>
<td>Sub</td>
<td class="samp_s">144</td>
<td>A=0.944</td>
<td>C=0.056</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013124">Central Asia</a>
</td>
<td>Sub</td>
<td class="samp_s">122</td>
<td>A=0.877</td>
<td>C=0.123</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013127">Europe</a>
</td>
<td>Sub</td>
<td class="samp_s">108</td>
<td>A=0.963</td>
<td>C=0.037</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013122">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">92</td>
<td>A=0.93</td>
<td>C=0.07</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
</td>
<td>
<a href="/biosample/SAMN13013125">Caucasus</a>
</td>
<td>Sub</td>
<td class="samp_s">36</td>
<td>A=0.89</td>
<td>C=0.11</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB5829">Genome of the Netherlands Release 5</a>
</td>
<td>
<a href="/biosample/SAMN13000132">Genome of the Netherlands</a>
</td>
<td>Study-wide</td>
<td class="samp_s">998</td>
<td>A=0.931</td>
<td>C=0.069</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB37584">CNV burdens in cranial meningiomas</a>
</td>
<td>
<a href="/biosample/SAMN15458720">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">764</td>
<td>A=0.949</td>
<td>C=0.051</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB37584">CNV burdens in cranial meningiomas</a>
</td>
<td>
<a href="/biosample/SAMN15458720">CRM</a>
</td>
<td>Sub</td>
<td class="samp_s">764</td>
<td>A=0.949</td>
<td>C=0.051</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA515199">A Vietnamese Genetic Variation Database</a>
</td>
<td>
<a href="/biosample/SAMN10744005">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">614</td>
<td>A=0.971</td>
<td>C=0.029</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PPRJNA503394">Northern Sweden</a>
</td>
<td>
<a href="/biosample/SAMN10359154">ACPOP</a>
</td>
<td>Study-wide</td>
<td class="samp_s">600</td>
<td>A=0.915</td>
<td>C=0.085</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB8705">Medical Genome Project healthy controls from Spanish population</a>
</td>
<td>
<a href="/biosample/SAMN13001620">Spanish controls</a>
</td>
<td>Study-wide</td>
<td class="samp_s">534</td>
<td>A=0.923</td>
<td>C=0.077</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7895">FINRISK</a>
</td>
<td>
<a href="/biosample/SAMN13002954">Finnish from FINRISK project</a>
</td>
<td>Study-wide</td>
<td class="samp_s">302</td>
<td>A=0.934</td>
<td>C=0.066</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA288297">Qatari</a>
</td>
<td>
<a href="/biosample/SAMN13019808">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">216</td>
<td>A=0.981</td>
<td>C=0.019</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA586841">SGDP_PRJ</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">80</td>
<td>A=0.47</td>
<td>C=0.53</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB36033">Ancient Sardinia genome-wide 1240k capture data generation and analysis</a>
</td>
<td>
<a href="/biosample/SAMN15458807">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">74</td>
<td>A=0.95</td>
<td>C=0.05</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA267856">Siberian</a>
</td>
<td>
<a href="/biosample/SAMN13113809">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">12</td>
<td>A=0.42</td>
<td>C=0.58</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="variant_details" class="js-tabcontent">
<a data-width="640px" href="#variant_details_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=variant_details_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="variant_details_tp" class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="variant_details_tp">
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with <a class="external-link" href="/variation/docs/glossary/#MolCon" rel="nofollow" target="_blank">molecular consequences</a> from <a class="external-link" href="http://www.sequenceontology.org/" rel="nofollow" target="_blank">Sequence Ontology</a>. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference &gt; Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.</p>
<div>
<div class="sect_heading">Genomic Placements</div>
<div id="gene_plac_allele">
<!-- display class is a short-cut for specifying the stripe hover order-column
row-border as the class name for a table -->
<table id="genomics_placements_table" class="stripe">
<thead>
<tr>
<th>Sequence name</th>
<th>Change</th>
</tr>
</thead>
<tbody>
<tr>
<td>GRCh38.p14 chr 10</td>
<td>NC_000010.11:g.94981296A>C</td>
</tr>
<tr>
<td>GRCh38.p14 chr 10</td>
<td>NC_000010.11:g.94981296A>G</td>
</tr>
<tr>
<td>GRCh37.p13 chr 10</td>
<td>NC_000010.10:g.96741053A>C</td>
</tr>
<tr>
<td>GRCh37.p13 chr 10</td>
<td>NC_000010.10:g.96741053A>G</td>
</tr>
<tr>
<td>CYP2C9 RefSeqGene (LRG_1195)</td>
<td>NG_008385.2:g.48139A>C</td>
</tr>
<tr>
<td>CYP2C9 RefSeqGene (LRG_1195)</td>
<td>NG_008385.2:g.48139A>G</td>
</tr>
</tbody>
</table>
</div>
<div id="trans_anno_allele">
<div class="sect_heading">
Gene: <a target="_blank" data-section="Variant Details"
data-ga-action="Click-on"
data-ga-label="transcript_annotation_gene_link"
ref="section=Variant Details&action=Click-on&label=transcript_annotation_gene_link"
href="/gene/1559">CYP2C9</a>, cytochrome P450 family 2 subfamily C member 9
(plus strand)
</div>
<table class="trans_anno_allele_datatable" class="stripe">
<thead>
<tr>
<th>Molecule type</th>
<th>Change</th>
<th>Amino acid[Codon]</th>
<th>SO Term</th>
</tr>
</thead>
<tbody>
<tr class="vard_odd">
<td>CYP2C9 transcript</td>
<td>
<span>
NM_000771.4:c.1075A>C
</span>
</td>
<td>
<span><span class="codon-plain">I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">] &gt; L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>cytochrome P450 2C9</td>
<td>
<span>
NP_000762.2:p.Ile359Leu
</span>
</td>
<td>
<span>
I (Ile) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>CYP2C9 transcript</td>
<td>
<span>
NM_000771.4:c.1075A>G
</span>
</td>
<td>
<span><span class="codon-plain">I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">] &gt; V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>cytochrome P450 2C9</td>
<td>
<span>
NP_000762.2:p.Ile359Val
</span>
</td>
<td>
<span>
I (Ile) > V (Val)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
</tbody>
</table>
</div>
</div>
</div>
<div id="clinical_significance" class="js-tabcontent">
<div>
<a data-width="640px" href="#clin_sig_tp"
ref="section=Clinical Significance&action=Click-on-Tooltip&label=clinical_significance_tp"
data-section="Clinical Significance" data-ga-action="Click-on-Tooltip"
data-ga-label="clinical_significance_tp"
class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="clin_sig_tp">
Clinical Significance tab shows a list of <a class="external-link" href="/clinvar/docs/clinsig" rel="nofollow" target="_blank">clinical significance </a>entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. <a href="/clinvar/RCV000001615.2" rel="nofollow" target="_blank">RCV000001615.2</a>) or Allele ID (i.e. <a href="/clinvar/variation/12274/" rel="nofollow" target="_blank">12274</a>) to access full ClinVar report.</p>
<div class="sect_heading">Allele: A= (allele ID:
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
target="_blank" href="/clinvar?term=(175053[AlleleID])"
data-section="Clinical Significance"
data-ga-action="Click-on"
data-ga-label="allele_link">
175053
</a>)
</div>
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
<thead>
<tr>
<th>ClinVar Accession</th>
<th>Disease Names</th>
<th>Clinical Significance</th>
</tr>
</thead>
<tbody>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000150377.13">RCV000150377.13</a>
</td>
<td>Warfarin response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000154312.13">RCV000154312.13</a>
</td>
<td>Warfarin response</td>
<td>Drug-Response</td>
</tr>
</tbody>
</table>
<div class="sect_heading">Allele: C (allele ID:
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
target="_blank" href="/clinvar?term=(23447[AlleleID])"
data-section="Clinical Significance"
data-ga-action="Click-on"
data-ga-label="allele_link">
23447
</a>)
</div>
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
<thead>
<tr>
<th>ClinVar Accession</th>
<th>Disease Names</th>
<th>Clinical Significance</th>
</tr>
</thead>
<tbody>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000008916.9">RCV000008916.9</a>
</td>
<td>Tolbutamide response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000008917.12">RCV000008917.12</a>
</td>
<td>Warfarin response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000008918.12">RCV000008918.12</a>
</td>
<td>Phenytoin response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000008919.11">RCV000008919.11</a>
</td>
<td>Glipizide response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000150378.13">RCV000150378.13</a>
</td>
<td>Warfarin response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000339502.12">RCV000339502.12</a>
</td>
<td>not provided</td>
<td>Other</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000787930.10">RCV000787930.10</a>
</td>
<td>Flurbiprofen response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000788094.10">RCV000788094.10</a>
</td>
<td>Lesinurad response</td>
<td>Drug-Response</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000788100.10">RCV000788100.10</a>
</td>
<td>Piroxicam response</td>
<td>Drug-Response</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="hgvs_tab" class="js-tabcontent">
<a data-width="640px" href="#aliases_tp"
ref="section=HGVS&action=Click-on-Tooltip&label=aliases_tp"
data-section="HGVS" data-ga-action="Click-on-Tooltip" data-ga-label="aliases_tp"
class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="aliases_tp">
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. <a href="http://varnomen.hgvs.org/">HGVS name</a> is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".</p>
<div id="hgvs">
<table id="alliases_alleles_datatable" class="stripe">
<thead class="allele_wrap">
<tr>
<th>Placement</th>
<th>
A=
</th>
<th>
C
</th>
<th>
G
</th>
</tr>
</thead>
<tbody class="allele_wrap">
<tr>
<td class="alias_hgvs">
GRCh38.p14 chr 10
</td>
<td class="alias_hgvs">
NC_000010.11:g.94981296=
</td>
<td class="alias_hgvs">
NC_000010.11:g.94981296A>C
</td>
<td class="alias_hgvs">
NC_000010.11:g.94981296A>G
</td>
</tr>
<tr>
<td class="alias_hgvs">
GRCh37.p13 chr 10
</td>
<td class="alias_hgvs">
NC_000010.10:g.96741053=
</td>
<td class="alias_hgvs">
NC_000010.10:g.96741053A>C
</td>
<td class="alias_hgvs">
NC_000010.10:g.96741053A>G
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP2C9 RefSeqGene (LRG_1195)
</td>
<td class="alias_hgvs">
NG_008385.2:g.48139=
</td>
<td class="alias_hgvs">
NG_008385.2:g.48139A>C
</td>
<td class="alias_hgvs">
NG_008385.2:g.48139A>G
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP2C9 transcript
</td>
<td class="alias_hgvs">
NM_000771.4:c.1075=
</td>
<td class="alias_hgvs">
NM_000771.4:c.1075A>C
</td>
<td class="alias_hgvs">
NM_000771.4:c.1075A>G
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP2C9 transcript
</td>
<td class="alias_hgvs">
NM_000771.3:c.1075=
</td>
<td class="alias_hgvs">
NM_000771.3:c.1075A>C
</td>
<td class="alias_hgvs">
NM_000771.3:c.1075A>G
</td>
</tr>
<tr>
<td class="alias_hgvs">
cytochrome P450 2C9
</td>
<td class="alias_hgvs">
NP_000762.2:p.Ile359=
</td>
<td class="alias_hgvs">
NP_000762.2:p.Ile359Leu
</td>
<td class="alias_hgvs">
NP_000762.2:p.Ile359Val
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="submissions" class="js-tabcontent">
<a data-width="640px" href="#submissions_tp"
ref="section=Submissions&action=Click-on-Tooltip&label=submissions_tp"
data-section="Submissions" data-ga-action="Click-on-Tooltip"
data-ga-label="submissions_tp" class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="submissions_tp">
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs).
We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time.
Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
</p>
<div class="sect_heading">
178 SubSNP,
31 Frequency,
11 ClinVar
submissions
</div>
<div id="submission">
<table id="submission_datatable" class="stripe">
<thead>
<tr>
<th>No</th>
<th>Submitter</th>
<th>Submission ID</th>
<th>Date (Build)</th>
</tr>
</thead>
<tbody>
<tr >
<td>1</td>
<td>
LEE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1538933">ss1538933</a>
</td>
<td>Oct 05, 2000
(86)
</td>
</tr>
<tr >
<td>2</td>
<td>
HGBASE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2419886">ss2419886</a>
</td>
<td>Nov 14, 2000
(89)
</td>
</tr>
<tr >
<td>3</td>
<td>
LEE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss4426472">ss4426472</a>
</td>
<td>May 29, 2002
(106)
</td>
</tr>
<tr >
<td>4</td>
<td>
SNP500CANCER
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5586419">ss5586419</a>
</td>
<td>Mar 31, 2003
(113)
</td>
</tr>
<tr >
<td>5</td>
<td>
EGP_SNPS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss12588583">ss12588583</a>
</td>
<td>Dec 05, 2003
(119)
</td>
</tr>
<tr >
<td>6</td>
<td>
IMCJ-GDT
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss28501344">ss28501344</a>
</td>
<td>Sep 24, 2004
(126)
</td>
</tr>
<tr >
<td>7</td>
<td>
BIOVENTURES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss32475993">ss32475993</a>
</td>
<td>May 24, 2005
(125)
</td>
</tr>
<tr >
<td>8</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss66633834">ss66633834</a>
</td>
<td>Nov 30, 2006
(127)
</td>
</tr>
<tr >
<td>9</td>
<td>
EGP_SNPS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss66862440">ss66862440</a>
</td>
<td>Nov 30, 2006
(127)
</td>
</tr>
<tr >
<td>10</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss66896412">ss66896412</a>
</td>
<td>Nov 30, 2006
(127)
</td>
</tr>
<tr >
<td>11</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss67006369">ss67006369</a>
</td>
<td>Nov 30, 2006
(127)
</td>
</tr>
<tr >
<td>12</td>
<td>
CSHL-HAPMAP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss68421487">ss68421487</a>
</td>
<td>Jan 12, 2007
(127)
</td>
</tr>
<tr >
<td>13</td>
<td>
PERLEGEN
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss69088153">ss69088153</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>14</td>
<td>
PHARMGKB_COBRA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss69365624">ss69365624</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>15</td>
<td>
PHARMGKB_PAT
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss69366288">ss69366288</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>16</td>
<td>
PHARMGKB_COBRA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss69366432">ss69366432</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>17</td>
<td>
PHARMGKB_COBRA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss69367461">ss69367461</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>18</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss70377003">ss70377003</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>19</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss70492465">ss70492465</a>
</td>
<td>May 26, 2008
(130)
</td>
</tr>
<tr >
<td>20</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss71017148">ss71017148</a>
</td>
<td>May 17, 2007
(127)
</td>
</tr>
<tr >
<td>21</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss75526698">ss75526698</a>
</td>
<td>Dec 07, 2007
(129)
</td>
</tr>
<tr >
<td>22</td>
<td>
SI_EXO
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss76884483">ss76884483</a>
</td>
<td>Dec 07, 2007
(129)
</td>
</tr>
<tr >
<td>23</td>
<td>
CCHMC-CAE-PGCORE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss79314175">ss79314175</a>
</td>
<td>Dec 16, 2007
(130)
</td>
</tr>
<tr >
<td>24</td>
<td>
KRIBB_YJKIM
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss83675538">ss83675538</a>
</td>
<td>Dec 16, 2007
(130)
</td>
</tr>
<tr >
<td>25</td>
<td>
PHARMGKB_AB_DME
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss84158157">ss84158157</a>
</td>
<td>Dec 16, 2007
(130)
</td>
</tr>
<tr >
<td>26</td>
<td>
PHARMGKB_PBAT
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss105107895">ss105107895</a>
</td>
<td>Feb 06, 2009
(130)
</td>
</tr>
<tr >
<td>27</td>
<td>
PHARMGKB_PEAR
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss105108091">ss105108091</a>
</td>
<td>Feb 06, 2009
(130)
</td>
</tr>
<tr >
<td>28</td>
<td>
PHARMGKB_PBAT
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss105109763">ss105109763</a>
</td>
<td>Feb 06, 2009
(130)
</td>
</tr>
<tr >
<td>29</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss121372691">ss121372691</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>30</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss152795933">ss152795933</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>31</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss159137280">ss159137280</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>32</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss161109628">ss161109628</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>33</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss169571265">ss169571265</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>34</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss170390048">ss170390048</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>35</td>
<td>
BCM-HGSC-SUB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss207372734">ss207372734</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>36</td>
<td>
1000GENOMES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss235293156">ss235293156</a>
</td>
<td>Jul 15, 2010
(132)
</td>
</tr>
<tr >
<td>37</td>
<td>
1000GENOMES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss241976260">ss241976260</a>
</td>
<td>Jul 15, 2010
(132)
</td>
</tr>
<tr >
<td>38</td>
<td>
OMICIA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss244238827">ss244238827</a>
</td>
<td>May 27, 2010
(132)
</td>
</tr>
<tr >
<td>39</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss244269683">ss244269683</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>40</td>
<td>
OMIM-CURATED-RECORDS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss256302165">ss256302165</a>
</td>
<td>Aug 26, 2010
(132)
</td>
</tr>
<tr >
<td>41</td>
<td>
NHLBI-ESP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss342304169">ss342304169</a>
</td>
<td>May 09, 2011
(134)
</td>
</tr>
<tr >
<td>42</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss410888155">ss410888155</a>
</td>
<td>Sep 17, 2011
(135)
</td>
</tr>
<tr >
<td>43</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss482693779">ss482693779</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>44</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss483026418">ss483026418</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>45</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss484045519">ss484045519</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>46</td>
<td>
1000GENOMES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491001674">ss491001674</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>47</td>
<td>
EXOME_CHIP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491438637">ss491438637</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>48</td>
<td>
CLINSEQ_SNP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491629979">ss491629979</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>49</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss536236827">ss536236827</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>50</td>
<td>
SSMP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss657186290">ss657186290</a>
</td>
<td>Apr 25, 2013
(138)
</td>
</tr>
<tr >
<td>51</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss778683444">ss778683444</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>52</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss780889011">ss780889011</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>53</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss782467384">ss782467384</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>54</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss783575257">ss783575257</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>55</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss825346614">ss825346614</a>
</td>
<td>Jul 19, 2016
(147)
</td>
</tr>
<tr >
<td>56</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss832649940">ss832649940</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>57</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss834142053">ss834142053</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>58</td>
<td>
JMKIDD_LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss974475598">ss974475598</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>59</td>
<td>
EVA-GONL
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss987806381">ss987806381</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>60</td>
<td>
JMKIDD_LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1067514968">ss1067514968</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>61</td>
<td>
JMKIDD_LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1077216799">ss1077216799</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>62</td>
<td>
1000GENOMES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1338631396">ss1338631396</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>63</td>
<td>
HAMMER_LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1397589497">ss1397589497</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>64</td>
<td>
EVA_FINRISK
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1584069489">ss1584069489</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>65</td>
<td>
EVA_DECODE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1597479676">ss1597479676</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>66</td>
<td>
EVA_UK10K_ALSPAC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1625199581">ss1625199581</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>67</td>
<td>
EVA_UK10K_TWINSUK
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1668193614">ss1668193614</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>68</td>
<td>
EVA_EXAC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1690012670">ss1690012670</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>69</td>
<td>
EVA_MGP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1711265826">ss1711265826</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>70</td>
<td>
EVA_SVP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1713202740">ss1713202740</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>71</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1751988390">ss1751988390</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>72</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1917849833">ss1917849833</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>73</td>
<td>
WEILL_CORNELL_DGM
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1931172559">ss1931172559</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>74</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1946289814">ss1946289814</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>75</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1959285055">ss1959285055</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>76</td>
<td>
AMU
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1966651107">ss1966651107</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>77</td>
<td>
JJLAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2026314474">ss2026314474</a>
</td>
<td>Sep 14, 2016
(149)
</td>
</tr>
<tr >
<td>78</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2094788887">ss2094788887</a>
</td>
<td>Dec 20, 2016
(150)
</td>
</tr>
<tr >
<td>79</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2095016478">ss2095016478</a>
</td>
<td>Dec 20, 2016
(150)
</td>
</tr>
<tr >
<td>80</td>
<td>
USC_VALOUEV
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2154591212">ss2154591212</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>81</td>
<td>
HUMAN_LONGEVITY
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2177161303">ss2177161303</a>
</td>
<td>Dec 20, 2016
(150)
</td>
</tr>
<tr >
<td>82</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2632748535">ss2632748535</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>83</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2632748536">ss2632748536</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>84</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2632748537">ss2632748537</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>85</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2632748538">ss2632748538</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>86</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2635018036">ss2635018036</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>87</td>
<td>
GRF
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2698844101">ss2698844101</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>88</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2710717613">ss2710717613</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>89</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2738421843">ss2738421843</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>90</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2748441781">ss2748441781</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>91</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2892149318">ss2892149318</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>92</td>
<td>
AFFY
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2984920017">ss2984920017</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>93</td>
<td>
AFFY
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2985568284">ss2985568284</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>94</td>
<td>
SWEGEN
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3006969228">ss3006969228</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>95</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3021264956">ss3021264956</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>96</td>
<td>
CSHL
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3349262052">ss3349262052</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>97</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3626510129">ss3626510129</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>98</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3626510130">ss3626510130</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>99</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3630771766">ss3630771766</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>100</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3634417926">ss3634417926</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>101</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3636102431">ss3636102431</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>102</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3637867360">ss3637867360</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>103</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3638949447">ss3638949447</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>104</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3639474781">ss3639474781</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>105</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3640125267">ss3640125267</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>106</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3642869426">ss3642869426</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>107</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3644542560">ss3644542560</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>108</td>
<td>
BIOINF_KMB_FNS_UNIBA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3645156529">ss3645156529</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>109</td>
<td>
OMUKHERJEE_ADBS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3646413639">ss3646413639</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>110</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3651623380">ss3651623380</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>111</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3651623381">ss3651623381</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>112</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3653690753">ss3653690753</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>113</td>
<td>
EGCUT_WGS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3674380916">ss3674380916</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>114</td>
<td>
EVA_DECODE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3690465147">ss3690465147</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>115</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3725179550">ss3725179550</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>116</td>
<td>
ACPOP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3737587066">ss3737587066</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>117</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3744369924">ss3744369924</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>118</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3744718895">ss3744718895</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>119</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3748470526">ss3748470526</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>120</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3772219251">ss3772219251</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>121</td>
<td>
KHV_HUMAN_GENOMES
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3813837035">ss3813837035</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>122</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3824541104">ss3824541104</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>123</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3825780791">ss3825780791</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>124</td>
<td>
HGDP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3847396074">ss3847396074</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>125</td>
<td>
SGDP_PRJ
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3874831499">ss3874831499</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>126</td>
<td>
KRGDB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3922960236">ss3922960236</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>127</td>
<td>
KOGIC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3968461756">ss3968461756</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>128</td>
<td>
FSA-LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3983983403">ss3983983403</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>129</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3984639065">ss3984639065</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>130</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3985493329">ss3985493329</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>131</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3986493499">ss3986493499</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>132</td>
<td>
TOPMED
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss4862693677">ss4862693677</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>133</td>
<td>
TOPMED
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss4862693678">ss4862693678</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>134</td>
<td>
TOMMO_GENOMICS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6114220328">ss6114220328</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>135</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6253834359">ss6253834359</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>136</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6307414007">ss6307414007</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>137</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6322395661">ss6322395661</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>138</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6332061248">ss6332061248</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>139</td>
<td>
YEGNASUBRAMANIAN_LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6343188435">ss6343188435</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>140</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6349787604">ss6349787604</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>141</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6349997715">ss6349997715</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>142</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6350060568">ss6350060568</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>143</td>
<td>
KOGIC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6382293375">ss6382293375</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>144</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6404050397">ss6404050397</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>145</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6404454521">ss6404454521</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>146</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6440428293">ss6440428293</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>147</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6440428294">ss6440428294</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>148</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6859935614">ss6859935614</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>149</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6859935615">ss6859935615</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>150</td>
<td>
TOMMO_GENOMICS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8198977293">ss8198977293</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>151</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8236886090">ss8236886090</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>152</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8237481940">ss8237481940</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>153</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8237481941">ss8237481941</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>154</td>
<td>
QINSY-LAB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8237630502">ss8237630502</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>155</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8237655814">ss8237655814</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>156</td>
<td>
1000G_HIGH_COVERAGE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8285094470">ss8285094470</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>157</td>
<td>
TRAN_CS_UWATERLOO
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8314429333">ss8314429333</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>158</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8315494592">ss8315494592</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>159</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8395333477">ss8395333477</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>160</td>
<td>
HUGCELL_USP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8480552797">ss8480552797</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>161</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8510130191">ss8510130191</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>162</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8512473914">ss8512473914</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>163</td>
<td>
1000G_HIGH_COVERAGE
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8579575173">ss8579575173</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>164</td>
<td>
SANFORD_IMAGENETICS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8624255749">ss8624255749</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>165</td>
<td>
SANFORD_IMAGENETICS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8649889766">ss8649889766</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>166</td>
<td>
TOMMO_GENOMICS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8745197781">ss8745197781</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>167</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8799403708">ss8799403708</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>168</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8800062051">ss8800062051</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>169</td>
<td>
YY_MCH
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8811794017">ss8811794017</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>170</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8824809647">ss8824809647</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>171</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8847378129">ss8847378129</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>172</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8847605672">ss8847605672</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>173</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8848304509">ss8848304509</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>174</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8849697687">ss8849697687</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>175</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8880092860">ss8880092860</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>176</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8941176035">ss8941176035</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>177</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8981728259">ss8981728259</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>178</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8982151878">ss8982151878</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>179</td>
<td>
1000Genomes
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>180</td>
<td>
1000Genomes_30X
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>181</td>
<td>
The Avon Longitudinal Study of Parents and Children
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>182</td>
<td>
Genome-wide autozygosity in Daghestan
</td>
<td>
NC_000010.9 - 96731043
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>183</td>
<td>
Genetic variation in the Estonian population
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>184</td>
<td>
ExAC
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>185</td>
<td>
FINRISK
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr class="disabled" >
<td>186</td>
<td>
<a href="#submission_tt_186"
data-ga-label="submission_tt_186" class="disabled">
gnomAD v4 - Exomes
</a>
<p id="submission_tt_186" class="break_values">
Submission ignored due to conflicting rows:<br>Row 35750133 (NC_000010.11:94981295:A:C 90936/1401270)<br>Row 35750134 (NC_000010.11:94981295:A:G 1/1401282)
</p>
</td>
<td>
-
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr class="disabled" >
<td>187</td>
<td>
<a href="#submission_tt_187"
data-ga-label="submission_tt_187" class="disabled">
gnomAD v4 - Exomes
</a>
<p id="submission_tt_187" class="break_values">
Submission ignored due to conflicting rows:<br>Row 35750133 (NC_000010.11:94981295:A:C 90936/1401270)<br>Row 35750134 (NC_000010.11:94981295:A:G 1/1401282)
</p>
</td>
<td>
-
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr class="disabled" >
<td>188</td>
<td>
<a href="#submission_tt_188"
data-ga-label="submission_tt_188" class="disabled">
gnomAD v4 - Genomes
</a>
<p id="submission_tt_188" class="break_values">
Submission ignored due to conflicting rows:<br>Row 387071403 (NC_000010.11:94981295:A:C 7381/149216)<br>Row 387071404 (NC_000010.11:94981295:A:G 1/149144)
</p>
</td>
<td>
-
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr class="disabled" >
<td>189</td>
<td>
<a href="#submission_tt_189"
data-ga-label="submission_tt_189" class="disabled">
gnomAD v4 - Genomes
</a>
<p id="submission_tt_189" class="break_values">
Submission ignored due to conflicting rows:<br>Row 387071403 (NC_000010.11:94981295:A:C 7381/149216)<br>Row 387071404 (NC_000010.11:94981295:A:G 1/149144)
</p>
</td>
<td>
-
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>190</td>
<td>
Genome of the Netherlands Release 5
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>191</td>
<td>
HGDP-CEPH-db Supplement 1
</td>
<td>
NC_000010.9 - 96731043
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>192</td>
<td>
HapMap
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>193</td>
<td>
KOREAN population from KRGDB
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>194</td>
<td>
Korean Genome Project
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>195</td>
<td>
Korean Genome Project 4K
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>196</td>
<td>
Medical Genome Project healthy controls from Spanish population
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>197</td>
<td>
Northern Sweden
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>198</td>
<td>
Ancient Sardinia genome-wide 1240k capture data generation and analysis
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>199</td>
<td>
CNV burdens in cranial meningiomas
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>200</td>
<td>
PharmGKB Aggregated
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>201</td>
<td>
Qatari
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>202</td>
<td>
SGDP_PRJ
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>203</td>
<td>
Siberian
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>204</td>
<td>
38KJPN
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr class="disabled" >
<td>205</td>
<td>
<a href="#submission_tt_205"
data-ga-label="submission_tt_205" class="disabled">
TopMed
</a>
<p id="submission_tt_205" class="break_values">
Submission ignored due to conflicting rows:<br>Row 78239332 (NC_000010.11:94981295:A:C 12238/264690)<br>Row 78239333 (NC_000010.11:94981295:A:G 1/264690)
</p>
</td>
<td>
-
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr class="disabled" >
<td>206</td>
<td>
<a href="#submission_tt_206"
data-ga-label="submission_tt_206" class="disabled">
TopMed
</a>
<p id="submission_tt_206" class="break_values">
Submission ignored due to conflicting rows:<br>Row 78239332 (NC_000010.11:94981295:A:C 12238/264690)<br>Row 78239333 (NC_000010.11:94981295:A:G 1/264690)
</p>
</td>
<td>
-
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>207</td>
<td>
UK 10K study - Twins
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>208</td>
<td>
A Vietnamese Genetic Variation Database
</td>
<td>
NC_000010.10 - 96741053
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>209</td>
<td>
ALFA
</td>
<td>
NC_000010.11 - 94981296
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>210</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000008916.9/">RCV000008916.9</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>211</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000008917.12/">RCV000008917.12</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>212</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000008918.12/">RCV000008918.12</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>213</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000008919.11/">RCV000008919.11</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>214</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000150377.13/">RCV000150377.13</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>215</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000150378.13/">RCV000150378.13</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>216</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000154312.13/">RCV000154312.13</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>217</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000339502.12/">RCV000339502.12</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>218</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000787930.10/">RCV000787930.10</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>219</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000788094.10/">RCV000788094.10</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
<tr >
<td>220</td>
<td>
ClinVar
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/clinvar/RCV000788100.10/">RCV000788100.10</a>
</td>
<td>Nov 01, 2024
(157)
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="history" class="js-tabcontent">
<a data-width="640px" href="#history_tp"
ref="section=History&action=Click-on-Tooltip&label=history_tp"
data-section="History" data-ga-action="Click-on-Tooltip" data-ga-label="history_tp"
class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="history_tp">
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).</p>
<div id="updt_hist">
<table id="up_hist_datatable" class="stripe">
<thead>
<tr>
<th>Associated ID</th>
<th>History Updated (Build)</th>
</tr>
</thead>
<tbody>
<tr>
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
data-ga-label="Associated_ID_link"
ref="section=History&action=Click-on&label=Associated_ID_link"
href="rs3198471">rs3198471</a>
</td>
<td>Jul 03, 2002
(106)
</td>
</tr>
<tr>
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
data-ga-label="Associated_ID_link"
ref="section=History&action=Click-on&label=Associated_ID_link"
href="rs17847042">rs17847042</a>
</td>
<td>Mar 10, 2006
(126)
</td>
</tr>
<tr>
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
data-ga-label="Associated_ID_link"
ref="section=History&action=Click-on&label=Associated_ID_link"
href="rs61212474">rs61212474</a>
</td>
<td>May 26, 2008
(130)
</td>
</tr>
</tbody>
</table>
</div>
<div id="obs_present">
<span>Added to this RefSNP Cluster:</span>
<table id="obs_present_table" class="observation_table stripe">
<thead>
<tr>
<th>Submission IDs</th>
<th>Observation <a href="/variation/notation/">SPDI</a></th>
<th>Canonical <a href="/variation/notation/">SPDI</a></th>
<th>Source RSIDs</th>
</tr>
</thead>
<tbody>
<tr>
<td>
ss3638949447,
ss3639474781
</td>
<td>
NC_000010.8:96731042:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
60926,
73966,
ss207372734,
ss482693779,
ss491629979,
ss825346614,
ss1397589497,
ss1597479676,
ss1713202740,
ss2635018036,
ss3642869426,
ss3847396074
</td>
<td>
NC_000010.9:96731042:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
51063033,
28349403,
20119164,
242346,
65950,
12641188,
30137630,
381586,
10871931,
719256,
188531,
13214489,
26848479,
7107566,
28349403,
6295229,
ss235293156,
ss241976260,
ss342304169,
ss483026418,
ss484045519,
ss491001674,
ss491438637,
ss536236827,
ss657186290,
ss778683444,
ss780889011,
ss782467384,
ss783575257,
ss832649940,
ss834142053,
ss974475598,
ss987806381,
ss1067514968,
ss1077216799,
ss1338631396,
ss1584069489,
ss1625199581,
ss1668193614,
ss1690012670,
ss1711265826,
ss1751988390,
ss1917849833,
ss1931172559,
ss1946289814,
ss1959285055,
ss1966651107,
ss2026314474,
ss2094788887,
ss2095016478,
ss2154591212,
ss2632748535,
ss2632748536,
ss2632748537,
ss2632748538,
ss2698844101,
ss2710717613,
ss2738421843,
ss2748441781,
ss2892149318,
ss2984920017,
ss2985568284,
ss3006969228,
ss3021264956,
ss3349262052,
ss3626510129,
ss3626510130,
ss3630771766,
ss3634417926,
ss3636102431,
ss3637867360,
ss3640125267,
ss3644542560,
ss3646413639,
ss3651623380,
ss3651623381,
ss3653690753,
ss3674380916,
ss3737587066,
ss3744369924,
ss3744718895,
ss3748470526,
ss3772219251,
ss3824541104,
ss3825780791,
ss3874831499,
ss3922960236,
ss3983983403,
ss3984639065,
ss3985493329,
ss3986493499,
ss6253834359,
ss6307414007,
ss6322395661,
ss6332061248,
ss6343188435,
ss6349787604,
ss6350060568,
ss6404454521,
ss8198977293,
ss8237481940,
ss8237481941,
ss8237630502,
ss8315494592,
ss8395333477,
ss8510130191,
ss8512473914,
ss8624255749,
ss8649889766,
ss8799403708,
ss8800062051,
ss8824809647,
ss8847378129,
ss8847605672,
ss8848304509,
ss8941176035,
ss8981728259,
ss8982151878
</td>
<td>
NC_000010.10:96741052:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
RCV000008916.9,
RCV000008917.12,
RCV000008918.12,
RCV000008919.11,
RCV000150378.13,
RCV000339502.12,
RCV000787930.10,
RCV000788094.10,
RCV000788100.10,
67101108,
468414,
24839757,
32145273,
1153,
131596148,
11541163928,
ss244238827,
ss256302165,
ss2177161303,
ss3645156529,
ss3690465147,
ss3725179550,
ss3813837035,
ss3968461756,
ss4862693677,
ss6114220328,
ss6349997715,
ss6382293375,
ss6404050397,
ss6440428293,
ss6859935614,
ss8236886090,
ss8237655814,
ss8285094470,
ss8314429333,
ss8480552797,
ss8579575173,
ss8745197781,
ss8811794017,
ss8849697687,
ss8880092860
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss76884483
</td>
<td>
NT_030059.12:15489578:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss1538933,
ss2419886,
ss4426472,
ss5586419,
ss12588583,
ss28501344,
ss32475993,
ss66633834,
ss66862440,
ss66896412,
ss67006369,
ss68421487,
ss69088153,
ss69365624,
ss69366288,
ss69366432,
ss69367461,
ss70377003,
ss70492465,
ss71017148,
ss75526698,
ss79314175,
ss83675538,
ss84158157,
ss105107895,
ss105108091,
ss105109763,
ss121372691,
ss152795933,
ss159137280,
ss161109628,
ss169571265,
ss170390048,
ss244269683,
ss410888155
</td>
<td>
NT_030059.13:47545516:A:C
</td>
<td>
NC_000010.11:94981295:A:C
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss2738421843
</td>
<td>
NC_000010.10:96741052:A:G
</td>
<td>
NC_000010.11:94981295:A:G
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
11541163928,
ss4862693678,
ss6440428294,
ss6859935615
</td>
<td>
NC_000010.11:94981295:A:G
</td>
<td>
NC_000010.11:94981295:A:G
</td>
<td>
(self)
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="publications" class="js-tabcontent">
<a data-width="640px" href="#publications_tp"
ref="section=Publications&action=Click-on-Tooltip&label=publications_tp"
data-section="Publications" data-ga-action="Click-on-Tooltip"
data-ga-label="publications_tp" class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="publications_tp">
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.</p>
<div class="sect_heading">
305
citations for rs1057910
</div>
<div id="publication">
<table id="publication_datatable" class="stripe">
<thead>
<tr>
<th>PMID</th>
<th class="fir_col">Title</th>
<th>Author</th>
<th>Year</th>
<th>Journal</th>
</tr>
</thead>
<tbody>
<tr>
<td><a target="_blank" href="/pubmed/8873220"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">8873220</a>
</td>
<td class="fir_col">The role of the CYP2C9-Leu359 allelic variant in the tolbutamide polymorphism.</td>
<td>Sullivan-Klose TH et al.</td>
<td>1996</td>
<td>Pharmacogenetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/9352571"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">9352571</a>
</td>
<td class="fir_col">Genetic association between sensitivity to warfarin and expression of CYP2C9*3.</td>
<td>Steward DJ et al.</td>
<td>1997</td>
<td>Pharmacogenetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/9630825"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">9630825</a>
</td>
<td class="fir_col">Metabolism of warfarin enantiomers in Japanese patients with heart disease having different CYP2C9 and CYP2C19 genotypes.</td>
<td>Takahashi H et al.</td>
<td>1998</td>
<td>Clinical pharmacology and therapeutics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/10073515"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">10073515</a>
</td>
<td class="fir_col">Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications.</td>
<td>Aithal GP et al.</td>
<td>1999</td>
<td>Lancet (London, England)</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/10208645"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">10208645</a>
</td>
<td class="fir_col">Pharmacokinetics of chlorpheniramine, phenytoin, glipizide and nifedipine in an individual homozygous for the CYP2C9*3 allele.</td>
<td>Kidd RS et al.</td>
<td>1999</td>
<td>Pharmacogenetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/10509530"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">10509530</a>
</td>
<td class="fir_col">CYP2C9*3 allelic variant and bleeding complications.</td>
<td>Ogg MS et al.</td>
<td>1999</td>
<td>Lancet (London, England)</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/10961881"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">10961881</a>
</td>
<td class="fir_col">Influence of cytochrome P-450 CYP2C9 polymorphisms on warfarin sensitivity and risk of over-anticoagulation in patients on long-term treatment.</td>
<td>Taube J et al.</td>
<td>2000</td>
<td>Blood</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/11127854"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">11127854</a>
</td>
<td class="fir_col">Genetic modulation of oral anticoagulation with warfarin.</td>
<td>Margaglione M et al.</td>
<td>2000</td>
<td>Thrombosis and haemostasis</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/11337938"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">11337938</a>
</td>
<td class="fir_col">In-vitro metabolism of celecoxib, a cyclooxygenase-2 inhibitor, by allelic variant forms of human liver microsomal cytochrome P450 2C9: correlation with CYP2C9 genotype and in-vivo pharmacokinetics.</td>
<td>Tang C et al.</td>
<td>2001</td>
<td>Pharmacogenetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/11692083"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">11692083</a>
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<td class="fir_col">Early acenocoumarol overanticoagulation among cytochrome P450 2C9 poor metabolizers.</td>
<td>Verstuyft C et al.</td>
<td>2001</td>
<td>Pharmacogenetics</td>
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<tr>
<td><a target="_blank" href="/pubmed/12893985"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">12893985</a>
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<td class="fir_col">Influence of CYP2C9 genetic polymorphisms on pharmacokinetics of celecoxib and its metabolites.</td>
<td>Kirchheiner J et al.</td>
<td>2003</td>
<td>Pharmacogenetics</td>
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<tr>
<td><a target="_blank" href="/pubmed/14707031"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">14707031</a>
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<td class="fir_col">Genetic predisposition to acute gastrointestinal bleeding after NSAIDs use.</td>
<td>Martínez C et al.</td>
<td>2004</td>
<td>British journal of pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/15116053"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">15116053</a>
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<td class="fir_col">Pharmacogenetics of acenocoumarol pharmacodynamics.</td>
<td>Morin S et al.</td>
<td>2004</td>
<td>Clinical pharmacology and therapeutics</td>
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<td><a target="_blank" href="/pubmed/15805193"
ref="section=Publications&action=Click-on&label=PMID_link"
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data-ga-label="PMID_link">15805193</a>
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<td class="fir_col">Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin.</td>
<td>Tate SK et al.</td>
<td>2005</td>
<td>Proceedings of the National Academy of Sciences of the United States of America</td>
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<tr>
<td><a target="_blank" href="/pubmed/16153401"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">16153401</a>
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<td class="fir_col">Cytochrome P450 2C9 genotype: impact on celecoxib safety and pharmacokinetics in a pediatric patient.</td>
<td>Stempak D et al.</td>
<td>2005</td>
<td>Clinical pharmacology and therapeutics</td>
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<tr>
<td><a target="_blank" href="/pubmed/16385451"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">16385451</a>
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<td class="fir_col">A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.</td>
<td>Grupe A et al.</td>
<td>2006</td>
<td>American journal of human genetics</td>
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<td><a target="_blank" href="/pubmed/16432637"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">16432637</a>
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<td class="fir_col">Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients.</td>
<td>Mushiroda T et al.</td>
<td>2006</td>
<td>Journal of human genetics</td>
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<tr>
<td><a target="_blank" href="/pubmed/17048007"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Association of warfarin dose with genes involved in its action and metabolism.</td>
<td>Wadelius M et al.</td>
<td>2007</td>
<td>Human genetics</td>
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<td><a target="_blank" href="/pubmed/17111199"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genotypes of the cytochrome p450 isoform, CYP2C9, and the vitamin K epoxide reductase complex subunit 1 conjointly determine stable warfarin dose: a prospective study.</td>
<td>Carlquist JF et al.</td>
<td>2006</td>
<td>Journal of thrombosis and thrombolysis</td>
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<td><a target="_blank" href="/pubmed/17368604"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">The association of CYP2C9 gene polymorphisms with colorectal carcinoma in Han Chinese.</td>
<td>Liao LH et al.</td>
<td>2007</td>
<td>Clinica chimica acta; international journal of clinical chemistry</td>
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<td><a target="_blank" href="/pubmed/17387222"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">17387222</a>
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<td class="fir_col">Genetic-based dosing in orthopedic patients beginning warfarin therapy.</td>
<td>Millican EA et al.</td>
<td>2007</td>
<td>Blood</td>
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<td><a target="_blank" href="/pubmed/17681167"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">17681167</a>
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<td class="fir_col">Genetic susceptibility to nonsteroidal anti-inflammatory drug-related gastroduodenal bleeding: role of cytochrome P450 2C9 polymorphisms.</td>
<td>Pilotto A et al.</td>
<td>2007</td>
<td>Gastroenterology</td>
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<td><a target="_blank" href="/pubmed/18030307"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Combination of phenotype assessments and CYP2C9-VKORC1 polymorphisms in the determination of warfarin dose requirements in heavily medicated patients.</td>
<td>Michaud V et al.</td>
<td>2008</td>
<td>Clinical pharmacology and therapeutics</td>
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<td><a target="_blank" href="/pubmed/18305455"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18305455</a>
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<td class="fir_col">Use of pharmacogenetic and clinical factors to predict the therapeutic dose of warfarin.</td>
<td>Gage BF et al.</td>
<td>2008</td>
<td>Clinical pharmacology and therapeutics</td>
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<tr>
<td><a target="_blank" href="/pubmed/18466099"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18466099</a>
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<td class="fir_col">Influence of CYP2C9 and VKORC1 on warfarin dose, anticoagulation attainment and maintenance among European-Americans and African-Americans.</td>
<td>Limdi NA et al.</td>
<td>2008</td>
<td>Pharmacogenomics</td>
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<tr>
<td><a target="_blank" href="/pubmed/18535201"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18535201</a>
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<td class="fir_col">A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.</td>
<td>Cooper GM et al.</td>
<td>2008</td>
<td>Blood</td>
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<td><a target="_blank" href="/pubmed/18542936"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18542936</a>
</td>
<td class="fir_col">VKORC1 and CYP2C9 polymorphisms are associated with warfarin dose requirements in Turkish patients.</td>
<td>Oner Ozgon G et al.</td>
<td>2008</td>
<td>European journal of clinical pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/18547414"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18547414</a>
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<td class="fir_col">Genotyping panel for assessing response to cancer chemotherapy.</td>
<td>Dai Z et al.</td>
<td>2008</td>
<td>BMC medical genomics</td>
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<td><a target="_blank" href="/pubmed/18574025"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18574025</a>
</td>
<td class="fir_col">The largest prospective warfarin-treated cohort supports genetic forecasting.</td>
<td>Wadelius M et al.</td>
<td>2009</td>
<td>Blood</td>
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<td><a target="_blank" href="/pubmed/18596683"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18596683</a>
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<td class="fir_col">Dosing algorithms to predict warfarin maintenance dose in Caucasians and African Americans.</td>
<td>Schelleman H et al.</td>
<td>2008</td>
<td>Clinical pharmacology and therapeutics</td>
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<td><a target="_blank" href="/pubmed/18662264"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18662264</a>
</td>
<td class="fir_col">Laboratory and clinical outcomes of pharmacogenetic vs. clinical protocols for warfarin initiation in orthopedic patients.</td>
<td>Lenzini PA et al.</td>
<td>2008</td>
<td>Journal of thrombosis and haemostasis </td>
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<td><a target="_blank" href="/pubmed/18680736"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18680736</a>
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<td class="fir_col">Genetic factors contribute to patient-specific warfarin dose for Han Chinese.</td>
<td>Wang TL et al.</td>
<td>2008</td>
<td>Clinica chimica acta; international journal of clinical chemistry</td>
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<td><a target="_blank" href="/pubmed/18752379"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18752379</a>
</td>
<td class="fir_col">Warfarin pharmacogenetics.</td>
<td>Limdi NA et al.</td>
<td>2008</td>
<td>Pharmacotherapy</td>
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<td><a target="_blank" href="/pubmed/18936436"
ref="section=Publications&action=Click-on&label=PMID_link"
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data-ga-label="PMID_link">18936436</a>
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<td class="fir_col">Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994.</td>
<td>Chang MH et al.</td>
<td>2009</td>
<td>American journal of epidemiology</td>
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<td><a target="_blank" href="/pubmed/18990750"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18990750</a>
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<td class="fir_col">Red meat intake, doneness, polymorphisms in genes that encode carcinogen-metabolizing enzymes, and colorectal cancer risk.</td>
<td>Cotterchio M et al.</td>
<td>2008</td>
<td>Cancer epidemiology, biomarkers & prevention </td>
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<td><a target="_blank" href="/pubmed/18992263"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18992263</a>
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<td class="fir_col">Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways.</td>
<td>Slattery ML et al.</td>
<td>2009</td>
<td>Mutation research</td>
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<td><a target="_blank" href="/pubmed/19177029"
ref="section=Publications&action=Click-on&label=PMID_link"
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data-ga-label="PMID_link">19177029</a>
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<td class="fir_col">Validation of VKORC1 and CYP2C9 genotypes on interindividual warfarin maintenance dose: a prospective study in Chinese patients.</td>
<td>Huang SW et al.</td>
<td>2009</td>
<td>Pharmacogenetics and genomics</td>
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<td><a target="_blank" href="/pubmed/19223558"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19223558</a>
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<td class="fir_col">Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.</td>
<td>Chang ET et al.</td>
<td>2009</td>
<td>Cancer epidemiology, biomarkers & prevention </td>
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<td><a target="_blank" href="/pubmed/19228618"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19228618</a>
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<td class="fir_col">Estimation of the warfarin dose with clinical and pharmacogenetic data.</td>
<td>Klein TE et al.</td>
<td>2009</td>
<td>The New England journal of medicine</td>
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<td><a target="_blank" href="/pubmed/19300499"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19300499</a>
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<td class="fir_col">A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.</td>
<td>Takeuchi F et al.</td>
<td>2009</td>
<td>PLoS genetics</td>
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<td><a target="_blank" href="/pubmed/19376514"
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data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19376514</a>
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<td class="fir_col">Association of cyclophosphamide drug-metabolizing enzyme polymorphisms and chemotherapy-related ovarian failure in breast cancer survivors.</td>
<td>Su HI et al.</td>
<td>2010</td>
<td>Fertility and sterility</td>
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<td><a target="_blank" href="/pubmed/19387626"
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data-ga-label="PMID_link">19387626</a>
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<td class="fir_col">Exploring warfarin pharmacogenomics with the extreme-discordant-phenotype methodology: impact of FVII polymorphisms on stable anticoagulation with warfarin.</td>
<td>Fuchshuber-Moraes M et al.</td>
<td>2009</td>
<td>European journal of clinical pharmacology</td>
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<td><a target="_blank" href="/pubmed/19422321"
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<td class="fir_col">Genetically based impairment in CYP2C8- and CYP2C9-dependent NSAID metabolism as a risk factor for gastrointestinal bleeding: is a combination of pharmacogenomics and metabolomics required to improve personalized medicine?</td>
<td>Agúndez JA et al.</td>
<td>2009</td>
<td>Expert opinion on drug metabolism & toxicology</td>
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<td><a target="_blank" href="/pubmed/19538716"
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<td class="fir_col">Thrombotic genetic risk factors and warfarin pharmacogenetic variants in São Miguel&#x27;s healthy population (Azores).</td>
<td>Branco CC et al.</td>
<td>2009</td>
<td>Thrombosis journal</td>
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<td class="fir_col">CYP2C9, CYP2C19, and ABCB1 genotype and hospitalization for phenytoin toxicity.</td>
<td>Hennessy S et al.</td>
<td>2009</td>
<td>Journal of clinical pharmacology</td>
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<td><a target="_blank" href="/pubmed/19679631"
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<td class="fir_col">Interactive modeling for ongoing utility of pharmacogenetic diagnostic testing: application for warfarin therapy.</td>
<td>Linder MW et al.</td>
<td>2009</td>
<td>Clinical chemistry</td>
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<td><a target="_blank" href="/pubmed/19694740"
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<td class="fir_col">No significant effect of ABCB1 haplotypes on the pharmacokinetics of fluvastatin, pravastatin, lovastatin, and rosuvastatin.</td>
<td>Keskitalo JE et al.</td>
<td>2009</td>
<td>British journal of clinical pharmacology</td>
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<td><a target="_blank" href="/pubmed/19794411"
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<td class="fir_col">Genetic factors (VKORC1, CYP2C9, EPHX1, and CYP4F2) are predictor variables for warfarin response in very elderly, frail inpatients.</td>
<td>Pautas E et al.</td>
<td>2010</td>
<td>Clinical pharmacology and therapeutics</td>
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<td><a target="_blank" href="/pubmed/19874474"
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<td class="fir_col">Ability of VKORC1 and CYP2C9 to predict therapeutic warfarin dose during the initial weeks of therapy.</td>
<td>Ferder NS et al.</td>
<td>2010</td>
<td>Journal of thrombosis and haemostasis </td>
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<td class="fir_col">Warfarin sensitivity genotyping: a review of the literature and summary of patient experience.</td>
<td>Moyer TP et al.</td>
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<td>Mayo Clinic proceedings</td>
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<td><a target="_blank" href="/pubmed/20017677"
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<td class="fir_col">ARMS test for diagnosis of CYP2C9 and VKORC1 mutation in patients with pulmonary embolism in Han Chinese.</td>
<td>Zhu J et al.</td>
<td>2010</td>
<td>Pharmacogenomics</td>
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<td><a target="_blank" href="/pubmed/20072124"
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<td class="fir_col">Genetic and clinical predictors of warfarin dose requirements in African Americans.</td>
<td>Cavallari LH et al.</td>
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<td>Clinical pharmacology and therapeutics</td>
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<td class="fir_col">Genetic variants involved in gallstone formation and capsaicin metabolism, and the risk of gallbladder cancer in Chilean women.</td>
<td>Báez S et al.</td>
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<td>World journal of gastroenterology</td>
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<td><a target="_blank" href="/pubmed/20149073"
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<td class="fir_col">Pharmacogenetics of acenocoumarol in patients with extreme dose requirements.</td>
<td>Pérez-Andreu V et al.</td>
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<td>Journal of thrombosis and haemostasis </td>
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<td><a target="_blank" href="/pubmed/20150829"
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<td class="fir_col">Cytochrome P450 2C9-CYP2C9.</td>
<td>Van Booven D et al.</td>
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<td class="fir_col">The genetics of ischaemic stroke.</td>
<td>Matarin M et al.</td>
<td>2010</td>
<td>Journal of internal medicine</td>
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<td><a target="_blank" href="/pubmed/20203262"
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<td class="fir_col">Warfarin pharmacogenetics: a single VKORC1 polymorphism is predictive of dose across 3 racial groups.</td>
<td>Limdi NA et al.</td>
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<td>Blood</td>
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<td><a target="_blank" href="/pubmed/20214591"
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<td class="fir_col">Cyclophosphamide-metabolizing enzyme polymorphisms and survival outcomes after adjuvant chemotherapy for node-positive breast cancer: a retrospective cohort study.</td>
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<td>Breast cancer research </td>
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<td class="fir_col">Worldwide allele frequency distribution of four polymorphisms associated with warfarin dose requirements.</td>
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<td>Journal of human genetics</td>
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<td class="fir_col">A novel, single algorithm approach to predict acenocoumarol dose based on CYP2C9 and VKORC1 allele variants.</td>
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<td>PloS one</td>
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<td class="fir_col">CYP4F2 rs2108622: a minor significant genetic factor of warfarin dose in Han Chinese patients with mechanical heart valve replacement.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Warfarin dosing in patients with impaired kidney function.</td>
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<td>American journal of kidney diseases </td>
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<td class="fir_col">New genetic variant that might improve warfarin dose prediction in African Americans.</td>
<td>Schelleman H et al.</td>
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<td>British journal of clinical pharmacology</td>
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<td><a target="_blank" href="/pubmed/20733952"
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<td class="fir_col">Warfarin genotyping using three different platforms.</td>
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<td>American journal of translational research</td>
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<td><a target="_blank" href="/pubmed/20808793"
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<td class="fir_col">Are cytochrome P450 CYP2C8 and CYP2C9 polymorphisms associated with ibuprofen response in very preterm infants?</td>
<td>Durrmeyer X et al.</td>
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<td>PloS one</td>
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<td class="fir_col">In pediatric patients, age has more impact on dosing of vitamin K antagonists than VKORC1 or CYP2C9 genotypes.</td>
<td>Nowak-Göttl U et al.</td>
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<td>Blood</td>
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<td class="fir_col">VKORC1-1639G&gt;A, CYP2C9, EPHX1691A&gt;G genotype, body weight, and age are important predictors for warfarin maintenance doses in patients with mechanical heart valve prostheses in southwest China.</td>
<td>Gu Q et al.</td>
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<td>European journal of clinical pharmacology</td>
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<td class="fir_col">Genotyping of DNA samples isolated from formalin-fixed paraffin-embedded tissues using preamplification.</td>
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<td>The Journal of molecular diagnostics </td>
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<td class="fir_col">Genotyping three SNPs affecting warfarin drug response by isothermal real-time HDA assays.</td>
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<td>Clinica chimica acta; international journal of clinical chemistry</td>
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<td class="fir_col">Mapping genes that predict treatment outcome in admixed populations.</td>
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<td>The pharmacogenomics journal</td>
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<td class="fir_col">Pharmacogenetics of Anti-Diabetes Drugs.</td>
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<td>Pharmaceuticals (Basel, Switzerland)</td>
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<td class="fir_col">Cigarette smoking, genetic variants in carcinogen-metabolizing enzymes, and colorectal cancer risk.</td>
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<td>American journal of epidemiology</td>
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<td class="fir_col">Prediction of phenprocoumon maintenance dose and phenprocoumon plasma concentration by genetic and non-genetic parameters.</td>
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<td>European journal of clinical pharmacology</td>
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<td class="fir_col">Contribution of VKORC1 and CYP2C9 polymorphisms in the interethnic variability of warfarin dose in Malaysian populations.</td>
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<td>Annals of hematology</td>
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<td class="fir_col">Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction.</td>
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<td>Journal of biomedicine & biotechnology</td>
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<td class="fir_col">Direct-to-Consumer Genetic and Genomic Testing: Preparing Nurse Practitioners for Genomic Healthcare.</td>
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<td>The journal for nurse practitioners </td>
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<td class="fir_col">Influence of CYP2C9 and VKORC1 polymorphisms on warfarin and acenocoumarol in a sample of Lebanese people.</td>
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<td class="fir_col">Amoxicillin/clavulanic acid-warfarin drug interaction: a randomized controlled trial.</td>
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<td class="fir_col">Genetic and nongenetic factors associated with warfarin dose requirements in Egyptian patients.</td>
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<td>Pharmacogenetics and genomics</td>
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<td class="fir_col">The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.</td>
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<td>Clinical pharmacology and therapeutics</td>
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<td class="fir_col">Influence of genetic, biological and pharmacological factors on warfarin dose in a Southern Brazilian population of European ancestry.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Translational aspects of genetic factors in the prediction of drug response variability: a case study of warfarin pharmacogenomics in a multi-ethnic cohort from Asia.</td>
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<td>The New England journal of medicine</td>
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<td class="fir_col">Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants.</td>
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<td class="fir_col">High-dimensional pharmacogenetic prediction of a continuous trait using machine learning techniques with application to warfarin dose prediction in African Americans.</td>
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<td>Bioinformatics (Oxford, England)</td>
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<td class="fir_col">Impact of CYP2D6, CYP3A5, CYP2C9 and CYP2C19 polymorphisms on tamoxifen pharmacokinetics in Asian breast cancer patients.</td>
<td>Lim JS et al.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Interaction between use of non-steroidal anti-inflammatory drugs and selected genetic polymorphisms in ovarian cancer risk.</td>
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<td>International journal of molecular epidemiology and genetics</td>
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<td class="fir_col">Identification of cytochrome P450 oxidoreductase gene variants that are significantly associated with the interindividual variations in warfarin maintenance dose.</td>
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<td>Drug metabolism and disposition</td>
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<td class="fir_col">Population diversity and the performance of warfarin dosing algorithms.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Genetic factors associated with patient-specific warfarin dose in ethnic Indonesians.</td>
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<td>BMC medical genetics</td>
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<td class="fir_col">Genetics of warfarin sensitivity in an emergency department population with thromboembolic.</td>
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<td>The western journal of emergency medicine</td>
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<td class="fir_col">Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis.</td>
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<td class="fir_col">Pharmacogenetic trial of a cannabinoid agonist shows reduced fasting colonic motility in patients with nonconstipated irritable bowel syndrome.</td>
<td>Wong BS et al.</td>
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<td>Gastroenterology</td>
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<td class="fir_col">Impact of genetic factors (VKORC1, CYP2C9, CYP4F2 and EPHX1) on the anticoagulation response to fluindione.</td>
<td>Lacut K et al.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Clinical Pharmacogenetics Implementation Consortium Guidelines for CYP2C9 and VKORC1 genotypes and warfarin dosing.</td>
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<td>Clinical pharmacology and therapeutics</td>
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<td class="fir_col">Pharmacogenomics: application to the management of cardiovascular disease.</td>
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<td class="fir_col">VKORC1 and CYP2C9 genotype and patient characteristics explain a large proportion of the variability in warfarin dose requirement among children.</td>
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<td class="fir_col">The pharmacogenetics of the response to warfarin in Chinese.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Clinical and genetic determinants of warfarin pharmacokinetics and pharmacodynamics during treatment initiation.</td>
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<td class="fir_col">The Creating an Optimal Warfarin Nomogram (CROWN) Study.</td>
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<td class="fir_col">Role of pharmacogenomics in the management of traditional and novel oral anticoagulants.</td>
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<td>Pharmacotherapy</td>
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<td class="fir_col">Pharmacogenetics in type 2 diabetes: potential implications for clinical practice.</td>
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<td>Genome medicine</td>
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<td class="fir_col">[Distribution of variant alleles association with warfarin pharmacokinetics and pharmacodynamics in the Han population in China].</td>
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<td>Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences</td>
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<td class="fir_col">Pharmacogenetic warfarin dose refinements remain significantly influenced by genetic factors after one week of therapy.</td>
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<td>Thrombosis and haemostasis</td>
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<td class="fir_col">Genetic polymorphisms are associated with variations in warfarin maintenance dose in Han Chinese patients with venous thromboembolism.</td>
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<td>Pharmacogenomics</td>
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<td>Carcinogenesis</td>
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<td class="fir_col">Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.</td>
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<td class="fir_col">Influence of genetics and non-genetic factors on acenocoumarol maintenance dose requirement in Moroccan patients.</td>
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<td>Journal of clinical pharmacy and therapeutics</td>
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<td>The pharmacogenomics journal</td>
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<td class="fir_col">Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population.</td>
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<td class="fir_col">PharmGKB summary: phenytoin pathway.</td>
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<td class="fir_col">Xenobiotic metabolizing gene variants and renal cell cancer: a multicenter study.</td>
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<td>Frontiers in oncology</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">Pharmacogenetic aspects of coumarinic oral anticoagulant therapies.</td>
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<td class="fir_col">An acenocoumarol dosing algorithm using clinical and pharmacogenetic data in Spanish patients with thromboembolic disease.</td>
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<td class="fir_col">Sequencing and analysis of a South Asian-Indian personal genome.</td>
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<td class="fir_col">Pharmacogenomics knowledge for personalized medicine.</td>
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<td>Clinical pharmacology and therapeutics</td>
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<td class="fir_col">CYP2C9 variants increase risk of colorectal adenoma recurrence and modify associations with smoking but not aspirin treatment.</td>
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<td class="fir_col">Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates.</td>
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<td class="fir_col">Influence of warfarin dose-associated genotypes on the risk of hemorrhagic complications in Chinese patients on warfarin.</td>
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<td>International journal of hematology</td>
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<td class="fir_col">Frequencies of 23 functionally significant variant alleles related with metabolism of antineoplastic drugs in the chilean population: comparison with caucasian and asian populations.</td>
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<td>Frontiers in genetics</td>
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<td class="fir_col">Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.</td>
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<td class="fir_col">Influence of ORM1 polymorphisms on the maintenance stable warfarin dosage.</td>
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<td class="fir_col">Pharmacogenetics of rheumatoid arthritis: Potential targets from susceptibility genes and present therapies.</td>
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<td class="fir_col">The role of genetics in pre-eclampsia and potential pharmacogenomic interventions.</td>
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<td class="fir_col">Efficiency and effectiveness of the use of an acenocoumarol pharmacogenetic dosing algorithm versus usual care in patients with venous thromboembolic disease initiating oral anticoagulation: study protocol for a randomized controlled trial.</td>
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<td class="fir_col">Positive selection in the chromosome 16 VKORC1 genomic region has contributed to the variability of anticoagulant response in humans.</td>
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<td class="fir_col">Effect of CYP2C9 and VKORC1 genetic polymorphisms on mean daily maintenance dose of acenocoumarol in South Indian patients.</td>
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<td class="fir_col">Effect of CYP2C9, VKORC1, CYP4F2 and GGCX genetic variants on warfarin maintenance dose and explicating a new pharmacogenetic algorithm in South Indian population.</td>
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<td class="fir_col">Genetic variants associated with phenytoin-related severe cutaneous adverse reactions.</td>
<td>Chung WH et al.</td>
<td>2014</td>
<td>JAMA</td>
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<td class="fir_col">A pharmacogenetics-based warfarin maintenance dosing algorithm from Northern Chinese patients.</td>
<td>Chen J et al.</td>
<td>2014</td>
<td>PloS one</td>
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<td><a target="_blank" href="/pubmed/25148255"
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<td class="fir_col">Determinants of the over-anticoagulation response during warfarin initiation therapy in Asian patients based on population pharmacokinetic-pharmacodynamic analyses.</td>
<td>Ohara M et al.</td>
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<td>PloS one</td>
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<td><a target="_blank" href="/pubmed/25168315"
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<td class="fir_col">Impact of genetic variability and treatment-related factors on outcome in early breast cancer patients receiving (neo-) adjuvant chemotherapy with 5-fluorouracil, epirubicin and cyclophosphamide, and docetaxel.</td>
<td>Vulsteke C et al.</td>
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<td>Breast cancer research and treatment</td>
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<td class="fir_col">Polymorphisms of cytochrome p450 genes in three ethnic groups from Russia.</td>
<td>Korytina G et al.</td>
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<td>Balkan medical journal</td>
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<td class="fir_col">Genetic markers in the EET metabolic pathway are associated with outcomes in patients with aneurysmal subarachnoid hemorrhage.</td>
<td>Donnelly MK et al.</td>
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<td>Journal of cerebral blood flow and metabolism </td>
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<td class="fir_col">Exploring the distribution of genetic markers of pharmacogenomics relevance in Brazilian and Mexican populations.</td>
<td>Bonifaz-Peña V et al.</td>
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<td class="fir_col">Genetic polymorphisms of ALOX5AP and CYP3A5 increase susceptibility to ischemic stroke and are associated with atherothrombotic events in stroke patients.</td>
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<td class="fir_col">Warfarin dosage response related pharmacogenetics in Chinese population.</td>
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<td class="fir_col">A systematic approach to the reporting of medically relevant findings from whole genome sequencing.</td>
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<td>BMC medical genetics</td>
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<td class="fir_col">The role of genotypes that modify the toxicity of chemical mutagens in the risk for myeloproliferative neoplasms.</td>
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<td>International journal of environmental research and public health</td>
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<td class="fir_col">Use of pharmacogenomics in pediatric renal transplant recipients.</td>
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<td>Frontiers in genetics</td>
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<td class="fir_col">CYP2C8 rs17110453 and EPHX2 rs751141 two-locus interaction increases susceptibility to ischemic stroke.</td>
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<td>Gene</td>
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<td><a target="_blank" href="/pubmed/25848132"
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<td class="fir_col">Effects of Pregnane X Receptor Genetic Polymorphisms on Stable Warfarin Doses.</td>
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<td>Journal of cardiovascular pharmacology and therapeutics</td>
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<td class="fir_col">Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.</td>
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<td>BMC genomics</td>
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<td class="fir_col">Influence of CYP2C9 polymorphism on the fall in International Normalized Ratio in patients interrupting warfarin therapy before elective surgery.</td>
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<td>Journal of thrombosis and haemostasis </td>
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<td class="fir_col">Influence of UDP-Glucuronosyltransferase Polymorphisms on Stable Warfarin Doses in Patients with Mechanical Cardiac Valves.</td>
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<td>Cardiovascular therapeutics</td>
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<td class="fir_col">Impact of regular physical activity on weekly warfarin dose requirement.</td>
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<td>Journal of thrombosis and thrombolysis</td>
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<td class="fir_col">Effects of single nucleotide polymorphisms in c-Myc on stable warfarin doses in patients with cardiac valve replacements.</td>
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<td>Pharmacogenomics</td>
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<td class="fir_col">Effects of NAD(P)H quinone oxidoreductase 1 polymorphisms on stable warfarin doses in Korean patients with mechanical cardiac valves.</td>
<td>Chung JE et al.</td>
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<td>European journal of clinical pharmacology</td>
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<td class="fir_col">Genome-wide association study of warfarin maintenance dose in a Brazilian sample.</td>
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<td>Pharmacogenomics</td>
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<td class="fir_col">Impact of New Genomic Technologies on Understanding Adverse Drug Reactions.</td>
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<td>Clinical pharmacokinetics</td>
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<td class="fir_col">High allele frequency of CYP2C9*3 (rs1057910) in a Negrito&#x27;s subtribe population in Malaysia; Aboriginal people of Jahai.</td>
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<td>Annals of human biology</td>
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<td class="fir_col">Pharmacogenetics of analgesic drugs.</td>
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<td class="fir_col">Effect of gene polymorphims on the warfarin treatment at initial stage.</td>
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<td>The pharmacogenomics journal</td>
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<td class="fir_col">A multi-factorial analysis of response to warfarin in a UK prospective cohort.</td>
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<td>Genome medicine</td>
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<td class="fir_col">Polymorphisms in genes involved in the absorption, distribution, metabolism, and excretion of drugs in the Kazakhs of Kazakhstan.</td>
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<td>BMC genetics</td>
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<td class="fir_col">Study of Clinical and Genetic Risk Factors for Aspirin-induced Gastric Mucosal Injury.</td>
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<td>Chinese medical journal</td>
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<td class="fir_col">Cross-Comparison of Exome Analysis, Next-Generation Sequencing of Amplicons, and the iPLEX(®) ADME PGx Panel for Pharmacogenomic Profiling.</td>
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<td>Frontiers in pharmacology</td>
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<td class="fir_col">Association of Cytochrome P450 Genetic Variants with Clopidogrel Resistance and Outcomes in Acute Ischemic Stroke.</td>
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<td>Journal of atherosclerosis and thrombosis</td>
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<td class="fir_col">A New Pharmacogenetic Algorithm to Predict the Most Appropriate Dosage of Acenocoumarol for Stable Anticoagulation in a Mixed Spanish Population.</td>
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<td class="fir_col">Interactions Among CYP2C8, EPHX2, and CYP4A11 Variants and CYP Plasma Metabolite Levels in Ischemic Stroke.</td>
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<td>Journal of atherosclerosis and thrombosis</td>
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<td class="fir_col">Effect of VKORC1, CYP2C9, CFP4F2, and GGCX Gene Polymorphisms on Warfarin Dose in Japanese Pediatric Patients.</td>
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<td>Molecular diagnosis & therapy</td>
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<td class="fir_col">ABCB1 polymorphism is associated with atorvastatin-induced liver injury in Japanese population.</td>
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<td class="fir_col">Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes.</td>
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<td>International journal of molecular sciences</td>
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<td class="fir_col">Prediction of Warfarin Dose in Pediatric Patients: An Evaluation of the Predictive Performance of Several Models.</td>
<td>Marek E et al.</td>
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<td>The journal of pediatric pharmacology and therapeutics </td>
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<td class="fir_col">The Risk of Congenital Heart Anomalies Following Prenatal Exposure to Serotonin Reuptake Inhibitors-Is Pharmacogenetics the Key?</td>
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<td>International journal of molecular sciences</td>
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<td class="fir_col">Pharmacogenetic studies update in type 2 diabetes mellitus.</td>
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<td>World journal of diabetes</td>
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<td class="fir_col">Impact of CYP2C9, VKORC1 and CYP4F2 genetic polymorphisms on maintenance warfarin dosage in Han-Chinese patients: A systematic review and meta-analysis.</td>
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<td class="fir_col">A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.</td>
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<td class="fir_col">Theory-based pharmacokinetics and pharmacodynamics of S- and R-warfarin and effects on international normalized ratio: influence of body size, composition and genotype in cardiac surgery patients.</td>
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<td>British journal of clinical pharmacology</td>
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<td class="fir_col">The effect of SNPs in CYP450 in chloroquine/primaquine Plasmodium vivax malaria treatment.</td>
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<td class="fir_col">Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.</td>
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<td class="fir_col">Clinical Pharmacogenetic Testing and Application: Laboratory Medicine Clinical Practice Guidelines.</td>
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<td class="fir_col">Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.</td>
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<td class="fir_col">Clinical and genetic factors associated with warfarin maintenance dose in northern Chinese patients with mechanical heart valve replacement.</td>
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<td>Medicine</td>
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<td class="fir_col">Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites.</td>
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<td class="fir_col">Polymorphisms of ESR1, UGT1A1, HCN1, MAP3K1 and CYP2B6 are associated with the prognosis of hormone receptor-positive early breast cancer.</td>
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<td class="fir_col">Influence of NR3C1 and VDR polymorphisms on stable warfarin dose in patients with mechanical cardiac valves.</td>
<td>Lee KE et al.</td>
<td>2017</td>
<td>International journal of cardiology</td>
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<td><a target="_blank" href="/pubmed/28321040"
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<td class="fir_col">Whole exome sequencing detects variants of genes that mediate response to anticancer drugs.</td>
<td>Ohnami S et al.</td>
<td>2017</td>
<td>The Journal of toxicological sciences</td>
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<td><a target="_blank" href="/pubmed/28384046"
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<td class="fir_col">Cross-Validation of High-Resolution Melting Analysis-Based Genotyping Platform.</td>
<td>Langaee T et al.</td>
<td>2017</td>
<td>Genetic testing and molecular biomarkers</td>
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<td><a target="_blank" href="/pubmed/28401802"
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<td class="fir_col">The Impact of Gene Polymorphisms on Anticoagulation Control With Warfarin.</td>
<td>Jiang HH et al.</td>
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<td>Clinical and applied thrombosis/hemostasis </td>
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<td><a target="_blank" href="/pubmed/28412319"
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<td class="fir_col">Genetic and Non-Genetic Factors Affecting the Quality of Anticoagulation Control and Vascular Events in Atrial Fibrillation.</td>
<td>Park YK et al.</td>
<td>2017</td>
<td>Journal of stroke and cerebrovascular diseases </td>
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<td><a target="_blank" href="/pubmed/28603633"
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<td class="fir_col">In vitro metabolism of exemestane by hepatic cytochrome P450s: impact of nonsynonymous polymorphisms on formation of the active metabolite 17β-dihydroexemestane.</td>
<td>Peterson A et al.</td>
<td>2017</td>
<td>Pharmacology research & perspectives</td>
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<td><a target="_blank" href="/pubmed/28620303"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Effect of Genetic Variability in the CYP4F2, CYP4F11, and CYP4F12 Genes on Liver mRNA Levels and Warfarin Response.</td>
<td>Zhang JE et al.</td>
<td>2017</td>
<td>Frontiers in pharmacology</td>
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<td><a target="_blank" href="/pubmed/28771511"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Exploring public genomics data for population pharmacogenomics.</td>
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<td>PloS one</td>
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<td class="fir_col">Pharmacogenetic determinants of outcomes on triplet hepatic artery infusion and intravenous cetuximab for liver metastases from colorectal cancer (European trial OPTILIV, NCT00852228).</td>
<td>Lévi F et al.</td>
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<td>British journal of cancer</td>
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<td><a target="_blank" href="/pubmed/28867752"
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<td class="fir_col">Genotyping of CYP2C9 and VKORC1 polymorphisms predicts south Indian patients with deep vein thrombosis as fast metabolizers of warfarin/acenocoumarin.</td>
<td>Arunkumar G et al.</td>
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<td>Drug discoveries & therapeutics</td>
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<td class="fir_col">Polymorphisms of vitamin K-related genes (EPHX1 and VKORC1L1) and stable warfarin doses.</td>
<td>Chung JE et al.</td>
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<td>Gene</td>
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<td><a target="_blank" href="/pubmed/29133890"
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<td class="fir_col">Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.</td>
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<td>Scientific reports</td>
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<td class="fir_col">Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 Years.</td>
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<td>Clinical and translational science</td>
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<td><a target="_blank" href="/pubmed/29218998"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">VKORC1-1639A allele influences warfarin maintenance dosage among Blacks receiving warfarin anticoagulation: a retrospective cohort study.</td>
<td>Mili FD et al.</td>
<td>2018</td>
<td>Future cardiology</td>
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<td class="fir_col">Genetic variation in biotransformation enzymes, air pollution exposures, and risk of spina bifida.</td>
<td>Padula AM et al.</td>
<td>2018</td>
<td>American journal of medical genetics. Part A</td>
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<td><a target="_blank" href="/pubmed/29776219"
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<td class="fir_col">A simulation of warfarin maintenance dose requirement using a pharmacogenetic algorithm in an ethnically diverse cohort.</td>
<td>Gladding P et al.</td>
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<td>Personalized medicine</td>
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<td><a target="_blank" href="/pubmed/29789925"
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<td class="fir_col">Associations of polymorphisms of CYP2D6 and CYP2C9 with early onset severe pre-eclampsia and response to labetalol therapy.</td>
<td>Sun CJ et al.</td>
<td>2018</td>
<td>Archives of gynecology and obstetrics</td>
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<td><a target="_blank" href="/pubmed/29950617"
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<td class="fir_col">Effects of SLCO1B1 and GATM gene variants on rosuvastatin-induced myopathy are unrelated to high plasma exposure of rosuvastatin and its metabolites.</td>
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<td>Acta pharmacologica Sinica</td>
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<td><a target="_blank" href="/pubmed/30068618"
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<td class="fir_col">Cohort Profile: the Predictors of Breast Cancer Recurrence (ProBe CaRE) Premenopausal Breast Cancer Cohort Study in Denmark.</td>
<td>Collin LJ et al.</td>
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<td>BMJ open</td>
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<td class="fir_col">Biological Predictors of Clozapine Response: A Systematic Review.</td>
<td>Samanaite R et al.</td>
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<td>Frontiers in psychiatry</td>
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<td class="fir_col">The role of pharmacogenetics of cytochrome P450s in phenytoin-induced DRESS syndrome.</td>
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<td>Central-European journal of immunology</td>
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<td class="fir_col">Influence of SLCO1B1 in gastric cancer patients treated with EOF chemotherapy.</td>
<td>Feng W et al.</td>
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<td>Oncology letters</td>
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<td class="fir_col">Genetic Polymorphisms and In Silico Mutagenesis Analyses of CYP2C9, CYP2D6, and CYPOR Genes in the Pakistani Population.</td>
<td>Ahmed S et al.</td>
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<td>Genes</td>
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<td><a target="_blank" href="/pubmed/30393497"
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<td class="fir_col">The significance of enzyme and transporter polymorphisms for imatinib plasma levels and achieving an optimal response in chronic myeloid leukemia patients.</td>
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<td>Archives of medical science </td>
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<td class="fir_col">Impact of CYP2C9 and VKORC1 Polymorphisms on Warfarin Sensitivity and Responsiveness in Jordanian Cardiovascular Patients during the Initiation Therapy.</td>
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<td>Genes</td>
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<td><a target="_blank" href="/pubmed/30515958"
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<td class="fir_col">Pharmacogenetics of type 2 diabetes mellitus, the route toward tailored medicine.</td>
<td>Mannino GC et al.</td>
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<td>Diabetes/metabolism research and reviews</td>
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<td><a target="_blank" href="/pubmed/30712247"
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<td class="fir_col">Interpretation of the effect of CYP2C9, VKORC1 and CYP4F2 variants on warfarin dosing adjustment in Turkey.</td>
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<td>Molecular biology reports</td>
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<td><a target="_blank" href="/pubmed/30758238"
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<td class="fir_col">Development and Cross-Validation of High-Resolution Melting Analysis-Based Cardiovascular Pharmacogenetics Genotyping Panel.</td>
<td>Langaee T et al.</td>
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<td>Genetic testing and molecular biomarkers</td>
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<td><a target="_blank" href="/pubmed/30866412"
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<td class="fir_col">VKORC1 and CYP2C9 Polymorphisms: A Case Report in a Dutch Family with Pulmonary Fibrosis.</td>
<td>Wijnen P et al.</td>
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<td>International journal of molecular sciences</td>
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<td><a target="_blank" href="/pubmed/30933373"
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<td class="fir_col">Warfarin dose requirement in patients having severe thrombosis or thrombophilia.</td>
<td>Helin TA et al.</td>
<td>2019</td>
<td>British journal of clinical pharmacology</td>
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<td><a target="_blank" href="/pubmed/31019283"
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<td class="fir_col">Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.</td>
<td>Thauvin-Robinet C et al.</td>
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<td>European journal of human genetics </td>
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<td><a target="_blank" href="/pubmed/31061616"
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<td class="fir_col">Effects of CYP2C9 and VKORC1 polymorphisms on warfarin sensitivity and responsiveness during the stabilization phase of therapy.</td>
<td>Al-Eitan LN et al.</td>
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<td>Saudi pharmaceutical journal </td>
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<td><a target="_blank" href="/pubmed/31086207"
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<td class="fir_col">Implications of genetic variation of common Drug Metabolizing Enzymes and ABC Transporters among the Pakistani Population.</td>
<td>Afsar NA et al.</td>
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<td>Scientific reports</td>
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<td><a target="_blank" href="/pubmed/31105858"
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<td class="fir_col">Impact of gene polymorphism on the initiation and maintenance phases of warfarin therapy in Chinese patients undergoing heart valve replacement.</td>
<td>Liu J et al.</td>
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<td>American journal of translational research</td>
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<td><a target="_blank" href="/pubmed/31411557"
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<td class="fir_col">Pharmacogenomic considerations for medications in the perioperative setting.</td>
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<td>Pharmacogenomics</td>
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<td class="fir_col">Polymorphisms of CYP2C9*2, CYP2C9*3 and VKORC1 genes related to time in therapeutic range in patients with atrial fibrillation using warfarin.</td>
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<td>The application of clinical genetics</td>
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<td><a target="_blank" href="/pubmed/31461081"
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<td class="fir_col">Association between HNF4A mutations and bleeding complications in patients with stable international normalized ratio.</td>
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<td>Pharmacogenetics and genomics</td>
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<td><a target="_blank" href="/pubmed/31584773"
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<td class="fir_col">Study of the allelic variants CYP2C9*2 and CYP2C9*3 in samples of the Peruvian mestizo population.</td>
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<td>Biomedica </td>
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<td class="fir_col">The presence of two reduced function variants in CYP2C9 influences the acute response to glipizide.</td>
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<td>Diabetic medicine </td>
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<td><a target="_blank" href="/pubmed/31854268"
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<td class="fir_col">Impact of CYP2C9, VKORC1, ApoE and ABCB1 polymorphisms on stable warfarin dose requirements in elderly Chinese patients.</td>
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<td>Pharmacogenomics</td>
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<td><a target="_blank" href="/pubmed/31869433"
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<td class="fir_col">Genetic Factors Influencing Warfarin Dose in Black-African Patients: A Systematic Review and Meta-Analysis.</td>
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<td>Clinical pharmacology and therapeutics</td>
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<td><a target="_blank" href="/pubmed/32228310"
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<td class="fir_col">Functionally Significant Coumarin-Related Variant Alleles and Time to Therapeutic Range in Chilean Cardiovascular Patients.</td>
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<td>Clinical and applied thrombosis/hemostasis </td>
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<td><a target="_blank" href="/pubmed/32253660"
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<td class="fir_col">Genetic polymorphisms of high platelet reactivity in Chinese patients with coronary heart disease under clopidogrel therapy.</td>
<td>Zou X et al.</td>
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<td>International journal of clinical pharmacy</td>
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<td><a target="_blank" href="/pubmed/32298597"
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<td class="fir_col">CYP Genotypes Are Associated with Toxicity and Survival in Osteosarcoma Patients.</td>
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<td>Journal of adolescent and young adult oncology</td>
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<td class="fir_col">Clinically relevant pharmacogenetic markers in Tatars and Balkars.</td>
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<td>Molecular biology reports</td>
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<td class="fir_col">Role of Genetic Variations in the Hepatic Handling of Drugs.</td>
<td>Marin JJG et al.</td>
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<td>International journal of molecular sciences</td>
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<td><a target="_blank" href="/pubmed/32327994"
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<td class="fir_col">A Pharmacogenetically Guided Acenocoumarol Dosing Algorithm for Chilean Patients: A Discovery Cohort Study.</td>
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<td>Frontiers in pharmacology</td>
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<td><a target="_blank" href="/pubmed/32332930"
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<td class="fir_col">Genotype-guided warfarin dosing may benefit patients with mechanical aortic valve replacements: randomized controlled study.</td>
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<td>Scientific reports</td>
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<td><a target="_blank" href="/pubmed/32380173"
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<td class="fir_col">Recommendations for Clinical Warfarin Genotyping Allele Selection: A Report of the Association for Molecular Pathology and the College of American Pathologists.</td>
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<td>The Journal of molecular diagnostics </td>
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<td><a target="_blank" href="/pubmed/32457604"
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<td class="fir_col">Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy.</td>
<td>Calderon-Ospina CA et al.</td>
<td>2020</td>
<td>Frontiers in pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/32559398"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Effects of EPHX1 rs2260863 polymorphisms on warfarin maintenance dose in very elderly, frail Han-Chinese population.</td>
<td>Lin X et al.</td>
<td>2020</td>
<td>Pharmacogenomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/32567426"
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<td class="fir_col">An association between the rs1799853 and rs1057910 polymorphisms of CYP2C9, the rs4244285 polymorphism of CYP2C19 and the prevalence rates of drug-resistant epilepsy in children.</td>
<td>Makowska M et al.</td>
<td>2021</td>
<td>The International journal of neuroscience</td>
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<tr>
<td><a target="_blank" href="/pubmed/32575674"
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<td class="fir_col">rs622342 in SLC22A1, CYP2C9*2 and CYP2C9*3 and Glycemic Response in Individuals with Type 2 Diabetes Mellitus Receiving Metformin/Sulfonylurea Combination Therapy: 6-Month Follow-Up Study.</td>
<td>Naja K et al.</td>
<td>2020</td>
<td>Journal of personalized medicine</td>
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<td><a target="_blank" href="/pubmed/32586526"
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<td class="fir_col">Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome.</td>
<td>Van Driest SL et al.</td>
<td>2020</td>
<td>The Journal of pediatrics</td>
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<tr>
<td><a target="_blank" href="/pubmed/32639515"
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<td class="fir_col">Bayesian Pathway Analysis for Complex Interactions.</td>
<td>Baurley JW et al.</td>
<td>2020</td>
<td>American journal of epidemiology</td>
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<td><a target="_blank" href="/pubmed/33192522"
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<td class="fir_col">Pleiotropic Functions of Cytochrome P450 Monooxygenase-Derived Eicosanoids in Cancer.</td>
<td>Luo Y et al.</td>
<td>2020</td>
<td>Frontiers in pharmacology</td>
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<td><a target="_blank" href="/pubmed/33262486"
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<td class="fir_col">Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.</td>
<td></td>
<td>2020</td>
<td>European journal of human genetics </td>
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<td><a target="_blank" href="/pubmed/33346480"
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<td class="fir_col">[The pharmacogenetics of hypoglycemia and the glycemic variability at the patients ith type 2 diabetes mellitus].</td>
<td>Chernikova NA et al.</td>
<td>2020</td>
<td>Terapevticheskii arkhiv</td>
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<td><a target="_blank" href="/pubmed/33519226"
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<td class="fir_col">Genetic Diversity of Drug-Related Genes in Native Americans of the Brazilian Amazon.</td>
<td>Fernandes MR et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
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<td><a target="_blank" href="/pubmed/33569925"
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<td class="fir_col">Gene-environment interactions between air pollution and biotransformation enzymes and risk of birth defects.</td>
<td>Padula AM et al.</td>
<td>2021</td>
<td>Birth defects research</td>
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<td><a target="_blank" href="/pubmed/33580125"
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<td class="fir_col">Preservation of epoxyeicosatrienoic acid bioavailability prevents renal allograft dysfunction and cardiovascular alterations in kidney transplant recipients.</td>
<td>Duflot T et al.</td>
<td>2021</td>
<td>Scientific reports</td>
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<td><a target="_blank" href="/pubmed/33637672"
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<td class="fir_col">Metabolism pathways of arachidonic acids: mechanisms and potential therapeutic targets.</td>
<td>Wang B et al.</td>
<td>2021</td>
<td>Signal transduction and targeted therapy</td>
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<td><a target="_blank" href="/pubmed/33804537"
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<td class="fir_col">Pharmacogenetics of Carbamazepine and Valproate: Focus on Polymorphisms of Drug Metabolizing Enzymes and Transporters.</td>
<td>Iannaccone T et al.</td>
<td>2021</td>
<td>Pharmaceuticals (Basel, Switzerland)</td>
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<td><a target="_blank" href="/pubmed/33805706"
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<td class="fir_col">SLCO1B1 Phenotype and CYP3A5 Polymorphism Significantly Affect Atorvastatin Bioavailability.</td>
<td>Zubiaur P et al.</td>
<td>2021</td>
<td>Journal of personalized medicine</td>
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<td><a target="_blank" href="/pubmed/33811620"
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<td class="fir_col">Influence of CYP2C9, VKORC1, and CYP4F2 polymorphisms on the pharmacodynamic parameters of warfarin: a cross-sectional study.</td>
<td>Sridharan K et al.</td>
<td>2021</td>
<td>Pharmacological reports </td>
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<td><a target="_blank" href="/pubmed/33840516"
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<td class="fir_col">Association Between the CYP2C9 Genotype and Hypoglycemia Among Patients With Type 2 Diabetes Receiving Sulfonylurea Treatment: A Meta-analysis.</td>
<td>Yee J et al.</td>
<td>2021</td>
<td>Clinical therapeutics</td>
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<td><a target="_blank" href="/pubmed/33995083"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Dexketoprofen Pharmacokinetics is not Significantly Altered by Genetic Polymorphism.</td>
<td>Mejía-Abril G et al.</td>
<td>2021</td>
<td>Frontiers in pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/34149005"
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<td class="fir_col">Sulfamethoxazole-trimethoprim-induced liver injury and genetic polymorphisms of NAT2 and CYP2C9 in Taiwan.</td>
<td>Huang YS et al.</td>
<td>2021</td>
<td>Pharmacogenetics and genomics</td>
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<tr>
<td><a target="_blank" href="/pubmed/34163711"
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<td class="fir_col">Universal and high-fidelity DNA single nucleotide polymorphism detection based on a CRISPR/Cas12a biochip.</td>
<td>Chen Y et al.</td>
<td>2021</td>
<td>Chemical science</td>
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<tr>
<td><a target="_blank" href="/pubmed/34250965"
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<td class="fir_col">Performance Evaluation of Warfarin Dose Prediction Algorithms and Effects of Clinical Factors on Warfarin Dose in Chinese Patients.</td>
<td>Gao W et al.</td>
<td>2021</td>
<td>Therapeutic drug monitoring</td>
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<tr>
<td><a target="_blank" href="/pubmed/34316407"
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<td class="fir_col">Efficacy of computational predictions of the functional effect of idiosyncratic pharmacogenetic variants.</td>
<td>McConnell H et al.</td>
<td>2021</td>
<td>PeerJ</td>
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<td><a target="_blank" href="/pubmed/34382722"
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<td class="fir_col">Profiling of warfarin pharmacokinetics-associated genetic variants: Black Africans portray unique genetic markers important for an African specific warfarin pharmacogenetics-dosing algorithm.</td>
<td>Ndadza A et al.</td>
<td>2021</td>
<td>Journal of thrombosis and haemostasis </td>
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<tr>
<td><a target="_blank" href="/pubmed/34385834"
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<td class="fir_col">Individualized Drugs&#x27; Selection by Evaluation of Drug Properties, Pharmacogenomics and Clinical Parameters: Performance of a Bioinformatic Tool Compared to a Clinically Established Counselling Process.</td>
<td>Borro M et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
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<tr>
<td><a target="_blank" href="/pubmed/34429635"
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<td class="fir_col">Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population.</td>
<td>He C et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
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<tr>
<td><a target="_blank" href="/pubmed/34498315"
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<td class="fir_col">The impact of an URAT1 polymorphism on the losartan treatment of hypertension and hyperuricemia.</td>
<td>Wu L et al.</td>
<td>2021</td>
<td>Journal of clinical laboratory analysis</td>
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<td><a target="_blank" href="/pubmed/34559488"
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<td class="fir_col">Retrospective pharmacogenetic analysis of a pediatric patient under anticoagulant treatment: Clinical case.</td>
<td>Cavieres M et al.</td>
<td>2021</td>
<td>Biomedica </td>
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<td><a target="_blank" href="/pubmed/34621165"
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<td class="fir_col">Lack of Major Involvement of Common CYP2C Gene Polymorphisms in the Risk of Developing Cross-Hypersensitivity to NSAIDs.</td>
<td>Macías Y et al.</td>
<td>2021</td>
<td>Frontiers in pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/34621706"
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<td class="fir_col">Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.</td>
<td>Kim B et al.</td>
<td>2021</td>
<td>Translational and clinical pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/34690761"
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<td class="fir_col">Effects of Cytochrome P450 and Transporter Polymorphisms on the Bioavailability and Safety of Dutasteride and Tamsulosin.</td>
<td>Villapalos-García G et al.</td>
<td>2021</td>
<td>Frontiers in pharmacology</td>
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<td><a target="_blank" href="/pubmed/34798807"
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<td class="fir_col">Genetic analysis of pharmacogenomic VIP variants in the Wa population from Yunnan Province of China.</td>
<td>Li D et al.</td>
<td>2021</td>
<td>BMC genomic data</td>
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<tr>
<td><a target="_blank" href="/pubmed/34802403"
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<td class="fir_col">Influence of CYP2C9 Polymorphisms on Plasma Concentration of Warfarin and 7-Hydroxy Warfarin in South Indian Patients.</td>
<td>Kumar DK et al.</td>
<td>2021</td>
<td>Current drug metabolism</td>
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<td><a target="_blank" href="/pubmed/34803393"
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<td class="fir_col">Pharmacogenomics and Personalized Medicine in Type 2 Diabetes Mellitus: Potential Implications for Clinical Practice.</td>
<td>Venkatachalapathy P et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
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<td><a target="_blank" href="/pubmed/34824904"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genetic diversity of &#x27;Very Important Pharmacogenes&#x27; in two South-Asian populations.</td>
<td>Bharti N et al.</td>
<td>2021</td>
<td>PeerJ</td>
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<td><a target="_blank" href="/pubmed/34900803"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">A pharmacogenetic pilot study of CYP2C9 common genetic variant and sulfonylureas therapeutic response in type 2 diabetes mellitus patients.</td>
<td>Didari E et al.</td>
<td>2021</td>
<td>Journal of diabetes and metabolic disorders</td>
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<td><a target="_blank" href="/pubmed/34920277"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Assessment of susceptibility to phthalate and DINCH exposure through CYP and UGT single nucleotide polymorphisms.</td>
<td>Stajnko A et al.</td>
<td>2022</td>
<td>Environment international</td>
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<td><a target="_blank" href="/pubmed/34949935"
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<td class="fir_col">Genetic Polymorphisms of Very Important Pharmacogene Variants in the Blang Population from Yunnan Province in China.</td>
<td>Wang Y et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/34958284"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Warfarin Pharmacogenomics for Precision Medicine in Real-Life Clinical Practice in Southern Africa: Harnessing 73 Variants in 29 Pharmacogenes.</td>
<td>Muyambo S et al.</td>
<td>2022</td>
<td>Omics </td>
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<td><a target="_blank" href="/pubmed/35089958"
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<td class="fir_col">Identification of pharmacogenetic variants from large scale next generation sequencing data in the Saudi population.</td>
<td>Goljan E et al.</td>
<td>2022</td>
<td>PloS one</td>
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<tr>
<td><a target="_blank" href="/pubmed/35136381"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genetic Analysis of CYP2C9 with Reference to Drug Response in Epilepsy Patients of Pakistan.</td>
<td>Maqbool H et al.</td>
<td>2022</td>
<td>Genetics research</td>
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<tr>
<td><a target="_blank" href="/pubmed/35169023"
ref="section=Publications&action=Click-on&label=PMID_link"
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</td>
<td class="fir_col"></td>
<td></td>
<td></td>
<td></td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/35337356"
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<td class="fir_col">Cross-ethnic analysis of common gene variants in hemostasis show lopsided representation of global populations in genetic databases.</td>
<td>Osman A et al.</td>
<td>2022</td>
<td>BMC medical genomics</td>
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<td><a target="_blank" href="/pubmed/35757332"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Determination of Pleiotropic Effect of Warfarin in VKORC1 and CYP2C9 Genotypes in Patients With Heart Valve Replacement.</td>
<td>Shafique H et al.</td>
<td>2022</td>
<td>Frontiers in cardiovascular medicine</td>
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<td><a target="_blank" href="/pubmed/35761855"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Pharmacogenetics of Breast Cancer Treatments: A Sub-Saharan Africa Perspective.</td>
<td>Nthontho KC et al.</td>
<td>2022</td>
<td>Pharmacogenomics and personalized medicine</td>
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<td><a target="_blank" href="/pubmed/35866816"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Impact of VKORC1, CYP2C9, CYP1A2, UGT1A1, and GGCX polymorphisms on warfarin maintenance dose: Exploring a new algorithm in South Chinese patients accept mechanical heart valve replacement.</td>
<td>Li J et al.</td>
<td>2022</td>
<td>Medicine</td>
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<td><a target="_blank" href="/pubmed/36065758"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">CYP2C8*3 and *4 define CYP2C8 phenotype: An approach with the substrate cinitapride.</td>
<td>Campodónico DM et al.</td>
<td>2022</td>
<td>Clinical and translational science</td>
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<td><a target="_blank" href="/pubmed/36076616"
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<td class="fir_col">Pharmacogenetics of siponimod: A systematic review.</td>
<td>Díaz-Villamarín X et al.</td>
<td>2022</td>
<td>Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie</td>
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<td><a target="_blank" href="/pubmed/36164570"
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<td class="fir_col">Prevalence of exposure to pharmacogenetic drugs by the Saudis treated at the health care centers of the Ministry of National Guard.</td>
<td>Alshabeeb MA et al.</td>
<td>2022</td>
<td>Saudi pharmaceutical journal </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/36210801"
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<td class="fir_col">A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients.</td>
<td>Asiimwe IG et al.</td>
<td>2022</td>
<td>Frontiers in pharmacology</td>
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<td><a target="_blank" href="/pubmed/36248867"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genetic factors underlying tacrolimus intolerance after liver transplantation.</td>
<td>Liu Y et al.</td>
<td>2022</td>
<td>Frontiers in immunology</td>
</tr>
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<td><a target="_blank" href="/pubmed/37457231"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Pharmacogenomics in the Management of Pulmonary Arterial Hypertension: Current Perspectives.</td>
<td>Coons JC et al.</td>
<td>2023</td>
<td>Pharmacogenomics and personalized medicine</td>
</tr>
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<td><a target="_blank" href="/pubmed/37686209"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Evaluation of Human Hepatocyte Drug Metabolism Carrying High-Risk or Protection-Associated Liver Disease Genetic Variants.</td>
<td>Faccioli LAP et al.</td>
<td>2023</td>
<td>International journal of molecular sciences</td>
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