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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/10264272"
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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">rs10264272</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>chr7:99665212 </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>
C>T
</dd>
<dt>Variation Type</dt>
<dd>
SNV
<span class="small-font gray">Single Nucleotide Variation</span>
</dd>
<dt>Frequency</dt>
<dd>
<div>
T=0.0041080
(5757/1401408, GnomAD_exomes)
</div><div>
T=0.007484
(2330/311328, ALFA)
</div><span>
T=0.042476 (11243/264690, TOPMED)
</span><span>(<a id="expandfrequency" data-freq-remn="15"
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">+ 15 more</a>)</span><div class="ui-widget hide_elm" id="remn_summ_freq"><div>
T=0.037488
(5594/149222, GnomAD_genomes)
</div><div>
T=0.011982
(1453/121268, ExAC)
</div><div>
T=0.06201
(4880/78700, PAGE_STUDY)
</div><div>
T=0.00001
(1/77444, 38KJPN)
</div><div>
T=0.04129
(537/13006, GO-ESP)
</div><div>
T=0.0465
(298/6404, 1000G_30X)
</div><div>
T=0.0445
(223/5008, 1000G)
</div><div>
T=0.0010
(4/3854, ALSPAC)
</div><div>
T=0.0000
(0/3708, TWINSUK)
</div><div>
T=0.0106
(35/3292, PRJNA289433)
</div><div>
T=0.0969
(139/1434, HapMap)
</div><div>
T=0.066
(54/816, PharmGKB)
</div><div>
T=0.006
(3/534, MGP)
</div><div>
T=0.032
(7/216, Qatari)
</div><div>
C=0.38
(12/32, SGDP_PRJ)
</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=((3210224[AlleleID]))">ClinVar</a>
</dd>
<dt>Gene : Consequence</dt>
<dd>
<div>CYP3A5 : Synonymous Variant</div><span>ZSCAN25 : Intron Variant</span>
</dd>
<dt>Publications</dt>
<dd>
<a id="snp_pub_count" href="#publications">53
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>
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<li class="js-tablist__item">
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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>
</li>
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ref="section=Tab&action=Click-on&label=Clinical Significance"
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Significance
<span aria-hidden="true"></span></a>
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<span aria-hidden="true"></span></a>
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data-ga-action="Click-on-horizontal" data-ga-label="Publications" id="label_id_seventh"
class="js-tablist__link">Publications
<span aria-hidden="true"></span></a>
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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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<a data-width="640px" href="#popfreq_tp"
ref="section=Frequency&action=Click-on-Popper&label=popfreq_tp"
data-section="Frequency" data-ga-action="Click-on-Popper"
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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">311328</td>
<td class="popfreq_ref_allele">C=0.992516</td>
<td class="popfreq_alt_allele">T=0.007484</td>
<td class="popfreq_alt_allele">0.985745</td>
<td class="popfreq_alt_allele">0.000713</td>
<td class="popfreq_alt_allele">0.013542</td>
<td class="popfreq_alt_allele">32</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492695">European</a>
</td>
<td>Sub</td>
<td class="samp_s">268326</td>
<td class="popfreq_ref_allele">C=0.998904</td>
<td class="popfreq_alt_allele">T=0.001096</td>
<td class="popfreq_alt_allele">0.997816</td>
<td class="popfreq_alt_allele">0.000007</td>
<td class="popfreq_alt_allele">0.002176</td>
<td class="popfreq_alt_allele">3</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492703">African</a>
</td>
<td>Sub</td>
<td class="samp_s">15664</td>
<td class="popfreq_ref_allele">C=0.88579</td>
<td class="popfreq_alt_allele">T=0.11421</td>
<td class="popfreq_alt_allele">0.784985</td>
<td class="popfreq_alt_allele">0.013407</td>
<td class="popfreq_alt_allele">0.201609</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">572</td>
<td class="popfreq_ref_allele">C=0.858</td>
<td class="popfreq_alt_allele">T=0.142</td>
<td class="popfreq_alt_allele">0.734266</td>
<td class="popfreq_alt_allele">0.017483</td>
<td class="popfreq_alt_allele">0.248252</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">15092</td>
<td class="popfreq_ref_allele">C=0.88683</td>
<td class="popfreq_alt_allele">T=0.11317</td>
<td class="popfreq_alt_allele">0.786907</td>
<td class="popfreq_alt_allele">0.013252</td>
<td class="popfreq_alt_allele">0.199841</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">3824</td>
<td class="popfreq_ref_allele">C=1.0000</td>
<td class="popfreq_alt_allele">T=0.0000</td>
<td class="popfreq_alt_allele">1.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">N/A</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492697">East Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">3112</td>
<td class="popfreq_ref_allele">C=1.0000</td>
<td class="popfreq_alt_allele">T=0.0000</td>
<td class="popfreq_alt_allele">1.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">N/A</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492701">Other Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">712</td>
<td class="popfreq_ref_allele">C=1.000</td>
<td class="popfreq_alt_allele">T=0.000</td>
<td class="popfreq_alt_allele">1.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">N/A</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492699">Latin American 1</a>
</td>
<td>Sub</td>
<td class="samp_s">1274</td>
<td class="popfreq_ref_allele">C=0.9537</td>
<td class="popfreq_alt_allele">T=0.0463</td>
<td class="popfreq_alt_allele">0.908948</td>
<td class="popfreq_alt_allele">0.00157</td>
<td class="popfreq_alt_allele">0.089482</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">1846</td>
<td class="popfreq_ref_allele">C=0.9908</td>
<td class="popfreq_alt_allele">T=0.0092</td>
<td class="popfreq_alt_allele">0.981582</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.018418</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492702">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">5218</td>
<td class="popfreq_ref_allele">C=1.0000</td>
<td class="popfreq_alt_allele">T=0.0000</td>
<td class="popfreq_alt_allele">1.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">N/A</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN11605645">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">15176</td>
<td class="popfreq_ref_allele">C=0.98873</td>
<td class="popfreq_alt_allele">T=0.01127</td>
<td class="popfreq_alt_allele">0.977992</td>
<td class="popfreq_alt_allele">0.000527</td>
<td class="popfreq_alt_allele">0.021481</td>
<td class="popfreq_alt_allele">6</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/rs10264272/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/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">1401408</td>
<td>C=0.9958920</td>
<td>T=0.0041080</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
European
</td>
<td>Sub</td>
<td class="samp_s">1165370</td>
<td>C=0.9993281</td>
<td>T=0.0006719</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
South Asian
</td>
<td>Sub</td>
<td class="samp_s">86254</td>
<td>C=0.99957</td>
<td>T=0.00043</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">44718</td>
<td>C=0.99045</td>
<td>T=0.00955</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
East Asian
</td>
<td>Sub</td>
<td class="samp_s">39700</td>
<td>C=1.00000</td>
<td>T=0.00000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">33464</td>
<td>C=0.86726</td>
<td>T=0.13274</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Ashkenazi Jewish
</td>
<td>Sub</td>
<td class="samp_s">26134</td>
<td>C=1.00000</td>
<td>T=0.00000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Middle Eastern
</td>
<td>sub</td>
<td class="samp_s">5768</td>
<td>C=0.9882</td>
<td>T=0.0118</td>
</tr>
<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">311328</td>
<td>C=0.992516</td>
<td>T=0.007484</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">268326</td>
<td>C=0.998904</td>
<td>T=0.001096</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">15664</td>
<td>C=0.88579</td>
<td>T=0.11421</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">15176</td>
<td>C=0.98873</td>
<td>T=0.01127</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">5218</td>
<td>C=1.0000</td>
<td>T=0.0000</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">3824</td>
<td>C=1.0000</td>
<td>T=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">1846</td>
<td>C=0.9908</td>
<td>T=0.0092</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">1274</td>
<td>C=0.9537</td>
<td>T=0.0463</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA400167">TopMed</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">264690</td>
<td>C=0.957524</td>
<td>T=0.042476</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">149222</td>
<td>C=0.962512</td>
<td>T=0.037488</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
European
</td>
<td>Sub</td>
<td class="samp_s">78618</td>
<td>C=0.99919</td>
<td>T=0.00081</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">41536</td>
<td>C=0.87553</td>
<td>T=0.12447</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">15292</td>
<td>C=0.97718</td>
<td>T=0.02282</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
East Asian
</td>
<td>Sub</td>
<td class="samp_s">5190</td>
<td>C=1.0000</td>
<td>T=0.0000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
South Asian
</td>
<td>Sub</td>
<td class="samp_s">4822</td>
<td>C=0.9996</td>
<td>T=0.0004</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Ashkenazi Jewish
</td>
<td>Sub</td>
<td class="samp_s">3470</td>
<td>C=1.0000</td>
<td>T=0.0000</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Middle Eastern
</td>
<td>sub</td>
<td class="samp_s">294</td>
<td>C=0.969</td>
<td>T=0.031</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">121268</td>
<td>C=0.988018</td>
<td>T=0.011982</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
Europe
</td>
<td>Sub</td>
<td class="samp_s">73276</td>
<td>C=0.99925</td>
<td>T=0.00075</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>C=0.99984</td>
<td>T=0.00016</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">11528</td>
<td>C=0.99202</td>
<td>T=0.00798</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>C=0.87572</td>
<td>T=0.12428</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">906</td>
<td>C=0.990</td>
<td>T=0.010</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868975">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">78700</td>
<td>C=0.93799</td>
<td>T=0.06201</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868721">AfricanAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">32516</td>
<td>C=0.88092</td>
<td>T=0.11908</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868735">Mexican</a>
</td>
<td>Sub</td>
<td class="samp_s">10808</td>
<td>C=0.99093</td>
<td>T=0.00907</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868722">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">8318</td>
<td>C=0.9999</td>
<td>T=0.0001</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868968">PuertoRican</a>
</td>
<td>Sub</td>
<td class="samp_s">7918</td>
<td>C=0.9442</td>
<td>T=0.0558</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868777">NativeHawaiian</a>
</td>
<td>Sub</td>
<td class="samp_s">4534</td>
<td>C=0.9967</td>
<td>T=0.0033</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868733">Cuban</a>
</td>
<td>Sub</td>
<td class="samp_s">4230</td>
<td>C=0.9792</td>
<td>T=0.0208</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868734">Dominican</a>
</td>
<td>Sub</td>
<td class="samp_s">3828</td>
<td>C=0.9365</td>
<td>T=0.0635</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868729">CentralAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">2450</td>
<td>C=0.9690</td>
<td>T=0.0310</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868969">SouthAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">1982</td>
<td>C=0.9894</td>
<td>T=0.0106</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868739">NativeAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">1260</td>
<td>C=0.9817</td>
<td>T=0.0183</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868970">SouthAsian</a>
</td>
<td>Sub</td>
<td class="samp_s">856</td>
<td>C=0.999</td>
<td>T=0.001</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>C=0.99999</td>
<td>T=0.00001</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">13006</td>
<td>C=0.95871</td>
<td>T=0.04129</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
</td>
<td>
European American
</td>
<td>Sub</td>
<td class="samp_s">8600</td>
<td>C=0.9992</td>
<td>T=0.0008</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
</td>
<td>
African American
</td>
<td>Sub</td>
<td class="samp_s">4406</td>
<td>C=0.8797</td>
<td>T=0.1203</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>C=0.9535</td>
<td>T=0.0465</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>C=0.8488</td>
<td>T=0.1512</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>C=0.9961</td>
<td>T=0.0039</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>C=1.0000</td>
<td>T=0.0000</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>C=1.0000</td>
<td>T=0.0000</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>C=0.977</td>
<td>T=0.023</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>C=0.9555</td>
<td>T=0.0445</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>C=0.8457</td>
<td>T=0.1543</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>C=1.0000</td>
<td>T=0.0000</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>C=0.9970</td>
<td>T=0.0030</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>C=1.000</td>
<td>T=0.000</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>C=0.977</td>
<td>T=0.023</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>C=0.9990</td>
<td>T=0.0010</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>C=1.0000</td>
<td>T=0.0000</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB37766">MxGDAR/Encodat-PGx</a>
</td>
<td>
<a href="/biosample/SAMN15457995">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">3292</td>
<td>C=0.9894</td>
<td>T=0.0106</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB37766">MxGDAR/Encodat-PGx</a>
</td>
<td>
MxGDAR
</td>
<td>Sub</td>
<td class="samp_s">3292</td>
<td>C=0.9894</td>
<td>T=0.0106</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">1434</td>
<td>C=0.9031</td>
<td>T=0.0969</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">692</td>
<td>C=0.819</td>
<td>T=0.181</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">314</td>
<td>C=0.962</td>
<td>T=0.038</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">252</td>
<td>C=0.996</td>
<td>T=0.004</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>C=0.994</td>
<td>T=0.006</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">816</td>
<td>C=0.934</td>
<td>T=0.066</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13099042">PA149794671</a>
</td>
<td>Sub</td>
<td class="samp_s">354</td>
<td>C=0.977</td>
<td>T=0.023</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13101623">PA164944472</a>
</td>
<td>Sub</td>
<td class="samp_s">268</td>
<td>C=0.854</td>
<td>T=0.146</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
</td>
<td>
<a href="/biosample/SAMN13097512">PA142202220</a>
</td>
<td>Sub</td>
<td class="samp_s">194</td>
<td>C=0.964</td>
<td>T=0.036</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>C=0.994</td>
<td>T=0.006</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>C=0.968</td>
<td>T=0.032</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">32</td>
<td>C=0.38</td>
<td>T=0.62</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 7</td>
<td>NC_000007.14:g.99665212C>T</td>
</tr>
<tr>
<td>GRCh37.p13 chr 7</td>
<td>NC_000007.13:g.99262835C>T</td>
</tr>
<tr>
<td>CYP3A5 RefSeqGene (LRG_1431)</td>
<td>NG_007938.2:g.19787G>A</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/221785">ZSCAN25</a>, zinc finger and SCAN domain containing 25
(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>ZSCAN25 transcript variant 7</td>
<td>
<span><a data-width="640px" href="#gene_change_12_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">NM_001350984.2:c.806-3883…</a><p id="gene_change_12_tp" class="break_values long_value_tooltip">NM_001350984.2:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant 8</td>
<td>
<span><a data-width="640px" href="#gene_change_22_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">NM_001350985.2:c.806-3883…</a><p id="gene_change_22_tp" class="break_values long_value_tooltip">NM_001350985.2:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant 2</td>
<td>
<span>
NM_001350979.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant 3</td>
<td>
<span>
NM_001350980.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant 4</td>
<td>
<span>
NM_001350981.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant 5</td>
<td>
<span>
NM_001350982.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant 6</td>
<td>
<span>
NM_001350983.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant 9</td>
<td>
<span>
NM_001350986.2:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant 1</td>
<td>
<span>
NM_145115.3:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X8</td>
<td>
<span><a data-width="640px" href="#gene_change_102_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">XM_011515909.3:c.806-3883…</a><p id="gene_change_102_tp" class="break_values long_value_tooltip">XM_011515909.3:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X9</td>
<td>
<span><a data-width="640px" href="#gene_change_112_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">XM_047420016.1:c.806-3883…</a><p id="gene_change_112_tp" class="break_values long_value_tooltip">XM_047420016.1:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X10</td>
<td>
<span><a data-width="640px" href="#gene_change_122_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">XM_047420017.1:c.806-3883…</a><p id="gene_change_122_tp" class="break_values long_value_tooltip">XM_047420017.1:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X13</td>
<td>
<span><a data-width="640px" href="#gene_change_132_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">XM_047420018.1:c.806-3883…</a><p id="gene_change_132_tp" class="break_values long_value_tooltip">XM_047420018.1:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X14</td>
<td>
<span><a data-width="640px" href="#gene_change_142_tp"
ref="section=Variant Details&action=Click-on-Tooltip&label=gene_change_tp"
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
data-ga-label="gene_change_tp" class="ncbiPopper">XM_047420019.1:c.806-3883…</a><p id="gene_change_142_tp" class="break_values long_value_tooltip">XM_047420019.1:c.806-3883C>T</p></span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X1</td>
<td>
<span>
XM_011515905.3:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X2</td>
<td>
<span>
XM_011515907.3:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X11</td>
<td>
<span>
XM_011515910.3:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X5</td>
<td>
<span>
XM_047420011.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X3</td>
<td>
<span>
XM_047420012.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X4</td>
<td>
<span>
XM_047420013.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X6</td>
<td>
<span>
XM_047420014.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X7</td>
<td>
<span>
XM_047420015.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X15</td>
<td>
<span>
XM_047420020.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X16</td>
<td>
<span>
XR_007059988.1:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X17</td>
<td>
<span>
XR_007059989.1:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_even">
<td>ZSCAN25 transcript variant X18</td>
<td>
<span>
XR_007059990.1:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
<tr class="vard_odd">
<td>ZSCAN25 transcript variant X12</td>
<td>
<span>
XR_927402.3:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron Variant
</td>
</tr>
</tbody>
</table>
<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/1577">CYP3A5</a>, cytochrome P450 family 3 subfamily A member 5
(minus 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>CYP3A5 transcript variant 2</td>
<td>
<span>
NM_001190484.3:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>CYP3A5 transcript variant 1</td>
<td>
<span>
NM_000777.5:c.624G>A
</span>
</td>
<td>
<span><span class="codon-plain">K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">G</span><span class="codon-plain">] &gt; K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">A</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>cytochrome P450 3A5 isoform 1</td>
<td>
<span>
NP_000768.1:p.Lys208=
</span>
</td>
<td>
<span>
K (Lys) > K (Lys)
</span>
</td>
<td>
Synonymous Variant
</td>
</tr>
<tr class="vard_odd">
<td>CYP3A5 transcript variant 4</td>
<td>
<span>
NM_001291829.2:c.285G>A
</span>
</td>
<td>
<span><span class="codon-plain">K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">G</span><span class="codon-plain">] &gt; K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">A</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>cytochrome P450 3A5 isoform 3</td>
<td>
<span>
NP_001278758.1:p.Lys95=
</span>
</td>
<td>
<span>
K (Lys) > K (Lys)
</span>
</td>
<td>
Synonymous Variant
</td>
</tr>
<tr class="vard_even">
<td>CYP3A5 transcript variant 5</td>
<td>
<span>
NM_001291830.2:c.594G>A
</span>
</td>
<td>
<span><span class="codon-plain">K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">G</span><span class="codon-plain">] &gt; K [</span><span class="codon-ghost">AA</span><span class="codon-hilite">A</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>cytochrome P450 3A5 isoform 4 precursor</td>
<td>
<span>
NP_001278759.1:p.Lys198=
</span>
</td>
<td>
<span>
K (Lys) > K (Lys)
</span>
</td>
<td>
Synonymous Variant
</td>
</tr>
<tr class="vard_odd">
<td>CYP3A5 transcript variant 3</td>
<td>
<span>
NR_033807.3:n.1243G>A
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Non Coding Transcript 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: T (allele ID:
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
target="_blank" href="/clinvar?term=(3210224[AlleleID])"
data-section="Clinical Significance"
data-ga-action="Click-on"
data-ga-label="allele_link">
3210224
</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/RCV003914459.1">RCV003914459.1</a>
</td>
<td>CYP3A5-related disorder</td>
<td>Likely-Benign</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>
C=
</th>
<th>
T
</th>
</tr>
</thead>
<tbody class="allele_wrap">
<tr>
<td class="alias_hgvs">
GRCh38.p14 chr 7
</td>
<td class="alias_hgvs">
NC_000007.14:g.99665212=
</td>
<td class="alias_hgvs">
NC_000007.14:g.99665212C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
GRCh37.p13 chr 7
</td>
<td class="alias_hgvs">
NC_000007.13:g.99262835=
</td>
<td class="alias_hgvs">
NC_000007.13:g.99262835C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 RefSeqGene (LRG_1431)
</td>
<td class="alias_hgvs">
NG_007938.2:g.19787=
</td>
<td class="alias_hgvs">
NG_007938.2:g.19787G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 1
</td>
<td class="alias_hgvs">
NM_000777.5:c.624=
</td>
<td class="alias_hgvs">
NM_000777.5:c.624G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 1
</td>
<td class="alias_hgvs">
NM_000777.4:c.624=
</td>
<td class="alias_hgvs">
NM_000777.4:c.624G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 1
</td>
<td class="alias_hgvs">
NM_000777.3:c.624=
</td>
<td class="alias_hgvs">
NM_000777.3:c.624G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 3
</td>
<td class="alias_hgvs">
NR_033807.3:n.1243=
</td>
<td class="alias_hgvs">
NR_033807.3:n.1243G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 3
</td>
<td class="alias_hgvs">
NR_033807.2:n.1273=
</td>
<td class="alias_hgvs">
NR_033807.2:n.1273G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 3
</td>
<td class="alias_hgvs">
NR_033807.1:n.1245=
</td>
<td class="alias_hgvs">
NR_033807.1:n.1245G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 4
</td>
<td class="alias_hgvs">
NM_001291829.2:c.285=
</td>
<td class="alias_hgvs">
NM_001291829.2:c.285G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 4
</td>
<td class="alias_hgvs">
NM_001291829.1:c.285=
</td>
<td class="alias_hgvs">
NM_001291829.1:c.285G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 5
</td>
<td class="alias_hgvs">
NM_001291830.2:c.594=
</td>
<td class="alias_hgvs">
NM_001291830.2:c.594G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 5
</td>
<td class="alias_hgvs">
NM_001291830.1:c.594=
</td>
<td class="alias_hgvs">
NM_001291830.1:c.594G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 5
</td>
<td class="alias_hgvs">
NR_033809.1:n.986=
</td>
<td class="alias_hgvs">
NR_033809.1:n.986G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 6
</td>
<td class="alias_hgvs">
NR_033810.1:n.1226=
</td>
<td class="alias_hgvs">
NR_033810.1:n.1226G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 4
</td>
<td class="alias_hgvs">
NR_033808.1:n.1226=
</td>
<td class="alias_hgvs">
NR_033808.1:n.1226G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 7
</td>
<td class="alias_hgvs">
NR_033811.1:n.975=
</td>
<td class="alias_hgvs">
NR_033811.1:n.975G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
CYP3A5 transcript variant 8
</td>
<td class="alias_hgvs">
NR_033812.1:n.867=
</td>
<td class="alias_hgvs">
NR_033812.1:n.867G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
cytochrome P450 3A5 isoform 1
</td>
<td class="alias_hgvs">
NP_000768.1:p.Lys208=
</td>
<td class="alias_hgvs">
NP_000768.1:p.Lys208=
</td>
</tr>
<tr>
<td class="alias_hgvs">
cytochrome P450 3A5 isoform 3
</td>
<td class="alias_hgvs">
NP_001278758.1:p.Lys95=
</td>
<td class="alias_hgvs">
NP_001278758.1:p.Lys95=
</td>
</tr>
<tr>
<td class="alias_hgvs">
cytochrome P450 3A5 isoform 4 precursor
</td>
<td class="alias_hgvs">
NP_001278759.1:p.Lys198=
</td>
<td class="alias_hgvs">
NP_001278759.1:p.Lys198=
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant 7
</td>
<td class="alias_hgvs">
NM_001350984.2:c.806-3883=
</td>
<td class="alias_hgvs">
NM_001350984.2:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant 8
</td>
<td class="alias_hgvs">
NM_001350985.2:c.806-3883=
</td>
<td class="alias_hgvs">
NM_001350985.2:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X5
</td>
<td class="alias_hgvs">
XM_005250198.1:c.806-11992=
</td>
<td class="alias_hgvs">
XM_005250198.1:c.806-11992C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X8
</td>
<td class="alias_hgvs">
XM_011515909.3:c.806-3883=
</td>
<td class="alias_hgvs">
XM_011515909.3:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X9
</td>
<td class="alias_hgvs">
XM_047420016.1:c.806-3883=
</td>
<td class="alias_hgvs">
XM_047420016.1:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X10
</td>
<td class="alias_hgvs">
XM_047420017.1:c.806-3883=
</td>
<td class="alias_hgvs">
XM_047420017.1:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X13
</td>
<td class="alias_hgvs">
XM_047420018.1:c.806-3883=
</td>
<td class="alias_hgvs">
XM_047420018.1:c.806-3883C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
ZSCAN25 transcript variant X14
</td>
<td class="alias_hgvs">
XM_047420019.1:c.806-3883=
</td>
<td class="alias_hgvs">
XM_047420019.1:c.806-3883C>T
</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">
112 SubSNP,
18 Frequency,
1 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>
WUGSC_SSAHASNP
</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=ss14134088">ss14134088</a>
</td>
<td>Dec 05, 2003
(119)
</td>
</tr>
<tr >
<td>2</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=ss32476142">ss32476142</a>
</td>
<td>May 24, 2005
(125)
</td>
</tr>
<tr >
<td>3</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=ss60197490">ss60197490</a>
</td>
<td>Oct 16, 2006
(127)
</td>
</tr>
<tr >
<td>4</td>
<td>
PHARMGKB_PAAR-UCHI
</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=ss69371787">ss69371787</a>
</td>
<td>May 18, 2007
(127)
</td>
</tr>
<tr >
<td>5</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=ss74883461">ss74883461</a>
</td>
<td>Dec 06, 2007
(129)
</td>
</tr>
<tr >
<td>6</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=ss79314231">ss79314231</a>
</td>
<td>Dec 15, 2007
(130)
</td>
</tr>
<tr >
<td>7</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=ss84155161">ss84155161</a>
</td>
<td>Dec 15, 2007
(130)
</td>
</tr>
<tr >
<td>8</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=ss105439784">ss105439784</a>
</td>
<td>Feb 05, 2009
(130)
</td>
</tr>
<tr >
<td>9</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=ss119619350">ss119619350</a>
</td>
<td>Dec 01, 2009
(131)
</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=ss152703961">ss152703961</a>
</td>
<td>Dec 01, 2009
(131)
</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=ss159119264">ss159119264</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>12</td>
<td>
SEATTLESEQ
</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=ss159715234">ss159715234</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>13</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=ss159884673">ss159884673</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>14</td>
<td>
PHARMGKB_PAAR-UCHI
</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=ss161109922">ss161109922</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>15</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=ss169949687">ss169949687</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>16</td>
<td>
BUSHMAN
</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=ss197976973">ss197976973</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>17</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=ss223228490">ss223228490</a>
</td>
<td>Jul 14, 2010
(132)
</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=ss244268485">ss244268485</a>
</td>
<td>Jul 04, 2010
(132)
</td>
</tr>
<tr >
<td>19</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=ss342240801">ss342240801</a>
</td>
<td>May 09, 2011
(134)
</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=ss479242577">ss479242577</a>
</td>
<td>May 04, 2012
(137)
</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=ss479245267">ss479245267</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>22</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=ss479604592">ss479604592</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>23</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=ss480387493">ss480387493</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>24</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=ss484421998">ss484421998</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>25</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=ss485503765">ss485503765</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>26</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=ss490949797">ss490949797</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>27</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=ss491910495">ss491910495</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>28</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=ss533712051">ss533712051</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>29</td>
<td>
TISHKOFF
</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=ss560183971">ss560183971</a>
</td>
<td>Apr 25, 2013
(138)
</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=ss779197459">ss779197459</a>
</td>
<td>Sep 08, 2015
(146)
</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=ss781218646">ss781218646</a>
</td>
<td>Sep 08, 2015
(146)
</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=ss782657458">ss782657458</a>
</td>
<td>Sep 08, 2015
(146)
</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=ss831907895">ss831907895</a>
</td>
<td>Sep 08, 2015
(146)
</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=ss832631995">ss832631995</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>35</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=ss834663060">ss834663060</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>36</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=ss974465102">ss974465102</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>37</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=ss1067490097">ss1067490097</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>38</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=ss1074831432">ss1074831432</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>39</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=ss1326337913">ss1326337913</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>40</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=ss1618799133">ss1618799133</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>41</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=ss1661793166">ss1661793166</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>42</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=ss1688840991">ss1688840991</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>43</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=ss1711173172">ss1711173172</a>
</td>
<td>Apr 01, 2015
(144)
</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=ss1752702668">ss1752702668</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>45</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=ss1927851259">ss1927851259</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>46</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=ss1946215402">ss1946215402</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>47</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=ss1959035635">ss1959035635</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>48</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=ss2296200866">ss2296200866</a>
</td>
<td>Dec 20, 2016
(150)
</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=ss2634638264">ss2634638264</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>50</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=ss2634638265">ss2634638265</a>
</td>
<td>Nov 08, 2017
(151)
</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=ss2634638266">ss2634638266</a>
</td>
<td>Nov 08, 2017
(151)
</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=ss2711117320">ss2711117320</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>53</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=ss2736598533">ss2736598533</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>54</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=ss2747871723">ss2747871723</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>55</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=ss2856765305">ss2856765305</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>56</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=ss2985413720">ss2985413720</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>57</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=ss2986045859">ss2986045859</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>58</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=ss3022760748">ss3022760748</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>59</td>
<td>
CSIRBIOHTS
</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=ss3029637921">ss3029637921</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>60</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=ss3625934032">ss3625934032</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>61</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=ss3629873017">ss3629873017</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>62</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=ss3632543889">ss3632543889</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>63</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=ss3633472116">ss3633472116</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>64</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=ss3634197467">ss3634197467</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>65</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=ss3635132965">ss3635132965</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>66</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=ss3635877051">ss3635877051</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>67</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=ss3636867351">ss3636867351</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>68</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=ss3637630065">ss3637630065</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>69</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=ss3638713083">ss3638713083</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>70</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=ss3640840257">ss3640840257</a>
</td>
<td>Oct 12, 2018
(152)
</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=ss3643647666">ss3643647666</a>
</td>
<td>Oct 12, 2018
(152)
</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=ss3644948505">ss3644948505</a>
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>73</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=ss3653294770">ss3653294770</a>
</td>
<td>Oct 12, 2018
(152)
</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=ss3654175332">ss3654175332</a>
</td>
<td>Oct 12, 2018
(152)
</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=ss3726465309">ss3726465309</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>76</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=ss3744293684">ss3744293684</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>77</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=ss3745432993">ss3745432993</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>78</td>
<td>
PAGE_CC
</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=ss3771386370">ss3771386370</a>
</td>
<td>Jul 13, 2019
(153)
</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=ss3772925844">ss3772925844</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>80</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=ss3810096644">ss3810096644</a>
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>81</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=ss3824296376">ss3824296376</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>82</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=ss3825724429">ss3825724429</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>83</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=ss3830722350">ss3830722350</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>84</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=ss3867981568">ss3867981568</a>
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>85</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=ss3984448806">ss3984448806</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>86</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=ss3986390917">ss3986390917</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>87</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=ss4017349809">ss4017349809</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>88</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=ss4756563862">ss4756563862</a>
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>89</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=ss6081190464">ss6081190464</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>90</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=ss6241635122">ss6241635122</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>91</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=ss6301280523">ss6301280523</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>92</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=ss6322314976">ss6322314976</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>93</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=ss6404379021">ss6404379021</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>94</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=ss6431767255">ss6431767255</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>95</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=ss6763863355">ss6763863355</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>96</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=ss8237035234">ss8237035234</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>97</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=ss8274031933">ss8274031933</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>98</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=ss8375496687">ss8375496687</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>99</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=ss8471003006">ss8471003006</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>100</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=ss8509064478">ss8509064478</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>101</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=ss8562812978">ss8562812978</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>102</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=ss8624169000">ss8624169000</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>103</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=ss8624670290">ss8624670290</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>104</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=ss8643587250">ss8643587250</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>105</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=ss8823255860">ss8823255860</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>106</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=ss8847323005">ss8847323005</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>107</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=ss8848146815">ss8848146815</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>108</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=ss8860087443">ss8860087443</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>109</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=ss8972771684">ss8972771684</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>110</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=ss8979835141">ss8979835141</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>111</td>
<td>
LNCC-LABINFO
</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=ss8982126870">ss8982126870</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>112</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=ss8982567030">ss8982567030</a>
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>113</td>
<td>
1000Genomes
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>114</td>
<td>
1000Genomes_30X
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>115</td>
<td>
The Avon Longitudinal Study of Parents and Children
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>116</td>
<td>
ExAC
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>117</td>
<td>
gnomAD v4 - Exomes
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>118</td>
<td>
gnomAD v4 - Genomes
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>119</td>
<td>
GO Exome Sequencing Project
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>120</td>
<td>
HapMap
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>121</td>
<td>
Medical Genome Project healthy controls from Spanish population
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>122</td>
<td>
The PAGE Study
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Jul 13, 2019
(153)
</td>
</tr>
<tr >
<td>123</td>
<td>
MxGDAR/Encodat-PGx
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>124</td>
<td>
PharmGKB Aggregated
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>125</td>
<td>
Qatari
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>126</td>
<td>
SGDP_PRJ
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Apr 26, 2020
(154)
</td>
</tr>
<tr >
<td>127</td>
<td>
38KJPN
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>128</td>
<td>
TopMed
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Apr 26, 2021
(155)
</td>
</tr>
<tr >
<td>129</td>
<td>
UK 10K study - Twins
</td>
<td>
NC_000007.13 - 99262835
</td>
<td>Oct 12, 2018
(152)
</td>
</tr>
<tr >
<td>130</td>
<td>
ALFA
</td>
<td>
NC_000007.14 - 99665212
</td>
<td>Oct 31, 2024
(157)
</td>
</tr>
<tr >
<td>131</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/RCV003914459.1/">RCV003914459.1</a>
</td>
<td>Oct 31, 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="rs58867275">rs58867275</a>
</td>
<td>May 25, 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>
ss197976973,
ss479242577,
ss485503765,
ss491910495,
ss3643647666
</td>
<td>
NC_000007.12:99100770:C:T
</td>
<td>
NC_000007.14:99665211:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
38351822,
21340760,
8914766,
754320,
288932,
1807,
9893189,
19998548,
21340760,
ss223228490,
ss342240801,
ss479245267,
ss479604592,
ss480387493,
ss484421998,
ss490949797,
ss533712051,
ss560183971,
ss779197459,
ss781218646,
ss782657458,
ss831907895,
ss832631995,
ss834663060,
ss974465102,
ss1067490097,
ss1074831432,
ss1326337913,
ss1618799133,
ss1661793166,
ss1688840991,
ss1711173172,
ss1752702668,
ss1927851259,
ss1946215402,
ss1959035635,
ss2634638264,
ss2634638265,
ss2634638266,
ss2711117320,
ss2736598533,
ss2747871723,
ss2856765305,
ss2985413720,
ss2986045859,
ss3022760748,
ss3029637921,
ss3625934032,
ss3629873017,
ss3632543889,
ss3633472116,
ss3634197467,
ss3635132965,
ss3635877051,
ss3636867351,
ss3637630065,
ss3638713083,
ss3640840257,
ss3644948505,
ss3653294770,
ss3654175332,
ss3744293684,
ss3745432993,
ss3772925844,
ss3824296376,
ss3825724429,
ss3830722350,
ss3867981568,
ss3984448806,
ss3986390917,
ss4017349809,
ss6241635122,
ss6301280523,
ss6322314976,
ss8375496687,
ss8509064478,
ss8624169000,
ss8624670290,
ss8643587250,
ss8823255860,
ss8847323005,
ss8848146815,
ss8972771684,
ss8979835141,
ss8982567030
</td>
<td>
NC_000007.13:99262834:C:T
</td>
<td>
NC_000007.14:99665211:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
RCV003914459.1,
50338913,
27082053,
290765241,
3455286,
607839,
11626,
98566284,
593941421,
12988334533,
ss2296200866,
ss3726465309,
ss3771386370,
ss3810096644,
ss4756563862,
ss6081190464,
ss6404379021,
ss6431767255,
ss6763863355,
ss8237035234,
ss8274031933,
ss8471003006,
ss8562812978,
ss8860087443,
ss8982126870
</td>
<td>
NC_000007.14:99665211:C:T
</td>
<td>
NC_000007.14:99665211:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss14134088
</td>
<td>
NT_007933.13:24496418:C:T
</td>
<td>
NC_000007.14:99665211:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss32476142,
ss60197490,
ss69371787,
ss74883461,
ss79314231,
ss84155161,
ss105439784,
ss119619350,
ss152703961,
ss159119264,
ss159715234,
ss159884673,
ss161109922,
ss169949687,
ss244268485
</td>
<td>
NT_007933.15:37295677:C:T
</td>
<td>
NC_000007.14:99665211:C:T
</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">
53
citations for rs10264272
</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/18341681"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18341681</a>
</td>
<td class="fir_col">Graft rejection: pharmacogenetic analysis or drug anamnesis?</td>
<td>Pham VV et al.</td>
<td>2008</td>
<td>British journal of clinical pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/18825162"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18825162</a>
</td>
<td class="fir_col">Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans.</td>
<td>Perera MA et al.</td>
<td>2009</td>
<td>The pharmacogenomics journal</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/20354687"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">20354687</a>
</td>
<td class="fir_col">Explaining variability in ciclosporin exposure in adult kidney transplant recipients.</td>
<td>Press RR et al.</td>
<td>2010</td>
<td>European journal of clinical pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/20459744"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">20459744</a>
</td>
<td class="fir_col">Cyclophosphamide-metabolizing enzyme polymorphisms and survival outcomes after adjuvant chemotherapy for node-positive breast cancer: a retrospective cohort study.</td>
<td>Gor PP et al.</td>
<td>2010</td>
<td>Breast cancer research </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/20959500"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">20959500</a>
</td>
<td class="fir_col">Induction of CYP3A4 by vinblastine: Role of the nuclear receptor NR1I2.</td>
<td>Smith NF et al.</td>
<td>2010</td>
<td>The Annals of pharmacotherapy</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21206424"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21206424</a>
</td>
<td class="fir_col">Novel polymorphisms associated with tacrolimus trough concentrations: results from a multicenter kidney transplant consortium.</td>
<td>Jacobson PA et al.</td>
<td>2011</td>
<td>Transplantation</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21712189"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21712189</a>
</td>
<td class="fir_col">Analysis of pharmacogenetic traits in two distinct South African populations.</td>
<td>Ikediobi O et al.</td>
<td>2011</td>
<td>Human genomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21806386"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21806386</a>
</td>
<td class="fir_col">Pharmacogenetics of calcineurin inhibitors in Brazilian renal transplant patients.</td>
<td>Santoro A et al.</td>
<td>2011</td>
<td>Pharmacogenomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21950641"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21950641</a>
</td>
<td class="fir_col">Effect of cytochrome P450 3A5 genotype on atorvastatin pharmacokinetics and its interaction with clarithromycin.</td>
<td>Shin J et al.</td>
<td>2011</td>
<td>Pharmacotherapy</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/22094953"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">22094953</a>
</td>
<td class="fir_col">Associations of ABCB1 3435C&gt;T and IL-10-1082G&gt;A polymorphisms with long-term sirolimus dose requirements in renal transplant patients.</td>
<td>Sam WJ et al.</td>
<td>2011</td>
<td>Transplantation</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/22445700"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">22445700</a>
</td>
<td class="fir_col">The impact of drug metabolizing enzyme polymorphisms on outcomes after antenatal corticosteroid use.</td>
<td>Haas DM et al.</td>
<td>2012</td>
<td>American journal of obstetrics and gynecology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/22808112"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">22808112</a>
</td>
<td class="fir_col">Liver enzyme abnormalities and associated risk factors in HIV patients on efavirenz-based HAART with or without tuberculosis co-infection in Tanzania.</td>
<td>Mugusi S et al.</td>
<td>2012</td>
<td>PloS one</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/22871999"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">22871999</a>
</td>
<td class="fir_col">Concordance of DMET plus genotyping results with those of orthogonal genotyping methods.</td>
<td>Fernandez CA et al.</td>
<td>2012</td>
<td>Clinical pharmacology and therapeutics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/23073467"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">23073467</a>
</td>
<td class="fir_col">Associations of ABCB1 and IL-10 genetic polymorphisms with sirolimus-induced dyslipidemia in renal transplant recipients.</td>
<td>Sam WJ et al.</td>
<td>2012</td>
<td>Transplantation</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/23133420"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">23133420</a>
</td>
<td class="fir_col">Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.</td>
<td>Suarez-Kurtz G et al.</td>
<td>2012</td>
<td>Frontiers in pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/23922006"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">23922006</a>
</td>
<td class="fir_col">PharmGKB summary: cyclosporine and tacrolimus pathways.</td>
<td>Barbarino JM et al.</td>
<td>2013</td>
<td>Pharmacogenetics and genomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/24427273"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">24427273</a>
</td>
<td class="fir_col">Global pharmacogenomics: distribution of CYP3A5 polymorphisms and phenotypes in the Brazilian population.</td>
<td>Suarez-Kurtz G et al.</td>
<td>2014</td>
<td>PloS one</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/24557078"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">24557078</a>
</td>
<td class="fir_col">Genomewide association study of atazanavir pharmacokinetics and hyperbilirubinemia in AIDS Clinical Trials Group protocol A5202.</td>
<td>Johnson DH et al.</td>
<td>2014</td>
<td>Pharmacogenetics and genomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/24944790"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">24944790</a>
</td>
<td class="fir_col">Screening for 392 polymorphisms in 141 pharmacogenes.</td>
<td>Kim JY et al.</td>
<td>2014</td>
<td>Biomedical reports</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/25266489"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">25266489</a>
</td>
<td class="fir_col">Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China.</td>
<td>Zhang J et al.</td>
<td>2014</td>
<td>BMC genetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/25741362"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">25741362</a>
</td>
<td class="fir_col">Use of pharmacogenomics in pediatric renal transplant recipients.</td>
<td>Medeiros M et al.</td>
<td>2015</td>
<td>Frontiers in genetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26091847"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">26091847</a>
</td>
<td class="fir_col">Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China.</td>
<td>Wang L et al.</td>
<td>2015</td>
<td>BMC genetics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26485092"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">26485092</a>
</td>
<td class="fir_col">Genomewide Association Study of Tacrolimus Concentrations in African American Kidney Transplant Recipients Identifies Multiple CYP3A5 Alleles.</td>
<td>Oetting WS et al.</td>
<td>2016</td>
<td>American journal of transplantation </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26667830"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">26667830</a>
</td>
<td class="fir_col">Genotype-guided tacrolimus dosing in African-American kidney transplant recipients.</td>
<td>Sanghavi K et al.</td>
<td>2017</td>
<td>The pharmacogenomics journal</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26779253"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
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<td class="fir_col">An Expanded Analysis of Pharmacogenetics Determinants of Efavirenz Response that Includes 3&#x27;-UTR Single Nucleotide Polymorphisms among Black South African HIV/AIDS Patients.</td>
<td>Swart M et al.</td>
<td>2015</td>
<td>Frontiers in genetics</td>
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<td><a target="_blank" href="/pubmed/26785747"
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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>
<td>Iskakova AN et al.</td>
<td>2016</td>
<td>BMC genetics</td>
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<td><a target="_blank" href="/pubmed/27233804"
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<td class="fir_col">Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China.</td>
<td>Jin T et al.</td>
<td>2016</td>
<td>BMC genetics</td>
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<td><a target="_blank" href="/pubmed/27767381"
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<td class="fir_col">The effect of SNPs in CYP450 in chloroquine/primaquine Plasmodium vivax malaria treatment.</td>
<td>Sortica VA et al.</td>
<td>2016</td>
<td>Pharmacogenomics</td>
</tr>
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<td><a target="_blank" href="/pubmed/28673292"
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<td class="fir_col">Effect of pharmacogenetics on plasma lumefantrine pharmacokinetics and malaria treatment outcome in pregnant women.</td>
<td>Mutagonda RF et al.</td>
<td>2017</td>
<td>Malaria journal</td>
</tr>
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<td><a target="_blank" href="/pubmed/29193749"
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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>
<td>Borobia AM et al.</td>
<td>2018</td>
<td>Clinical and translational science</td>
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<td><a target="_blank" href="/pubmed/29681089"
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</td>
<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>
</tr>
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<td><a target="_blank" href="/pubmed/29775201"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Tacrolimus Population Pharmacokinetics and Multiple CYP3A5 Genotypes in Black and White Renal Transplant Recipients.</td>
<td>Campagne O et al.</td>
<td>2018</td>
<td>Journal of clinical pharmacology</td>
</tr>
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<td><a target="_blank" href="/pubmed/30093869"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Biological Predictors of Clozapine Response: A Systematic Review.</td>
<td>Samanaite R et al.</td>
<td>2018</td>
<td>Frontiers in psychiatry</td>
</tr>
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<td><a target="_blank" href="/pubmed/30801552"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genetic Variants Associated With Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome-wide Association Studies.</td>
<td>Oetting WS et al.</td>
<td>2019</td>
<td>Transplantation</td>
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<td><a target="_blank" href="/pubmed/30953600"
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<td class="fir_col">Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups.</td>
<td>Mohamed ME et al.</td>
<td>2019</td>
<td>American journal of transplantation </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/32366712"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Influence of CYP2C8, CYP3A4, and CYP3A5 Host Genotypes on Early Recurrence of Plasmodium vivax.</td>
<td>Almeida ACG et al.</td>
<td>2020</td>
<td>Antimicrobial agents and chemotherapy</td>
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<td><a target="_blank" href="/pubmed/32847973"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Phase I, Pharmacogenomic, Drug Interaction Study of Sorafenib and Bevacizumab in Combination with Paclitaxel in Patients with Advanced Refractory Solid Tumors.</td>
<td>Chiorean EG et al.</td>
<td>2020</td>
<td>Molecular cancer therapeutics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/33519226"
ref="section=Publications&action=Click-on&label=PMID_link"
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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>
</tr>
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<td><a target="_blank" href="/pubmed/33805706"
ref="section=Publications&action=Click-on&label=PMID_link"
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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/33829662"
ref="section=Publications&action=Click-on&label=PMID_link"
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<td class="fir_col">Genetic variants related to successful migraine prophylaxis with verapamil.</td>
<td>Cutrer FM et al.</td>
<td>2021</td>
<td>Molecular genetics & genomic medicine</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/33995083"
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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>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/34262462"
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<td class="fir_col">Pharmacogenomics of Impaired Tyrosine Kinase Inhibitor Response: Lessons Learned From Chronic Myelogenous Leukemia.</td>
<td>Kaehler M et al.</td>
<td>2021</td>
<td>Frontiers in pharmacology</td>
</tr>
<tr>
<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>
</tr>
<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>
</tr>
<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>
</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/34974452"
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<td class="fir_col">The Impact of Donor and Recipient Genetic Variation on Outcomes After Solid Organ Transplantation: A Scoping Review and Future Perspectives.</td>
<td>Li Y et al.</td>
<td>2022</td>
<td>Transplantation</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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<td><a target="_blank" href="/pubmed/35158880"
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<td class="fir_col">Pharmacogenomics of Vincristine-Induced Peripheral Neuropathy in Children with Cancer: A Systematic Review and Meta-Analysis.</td>
<td>Uittenboogaard A et al.</td>
<td>2022</td>
<td>Cancers</td>
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<tr>
<td><a target="_blank" href="/pubmed/35761855"
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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/35846994"
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<td class="fir_col">Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing.</td>
<td>Silgado-Guzmán DF et al.</td>
<td>2022</td>
<td>Frontiers in pharmacology</td>
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<tr>
<td><a target="_blank" href="/pubmed/36065758"
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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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<tr>
<td><a target="_blank" href="/pubmed/36164570"
ref="section=Publications&action=Click-on&label=PMID_link"
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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>
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