dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs5030868
Current Build 157
Released September 3, 2024
- Organism
- Homo sapiens
- Position
-
chrX:154534419 (GRCh38.p14) Help
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 here for details.
- Alleles
- G>A
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.0014023 (1475/1051813, GnomAD_exomes)A=0.000559 (148/264690, TOPMED)A=0.001386 (263/189758, ALFA) (+ 8 more)
- Clinical Significance
- Reported in ClinVar
- Gene : Consequence
- G6PD : Missense Variant
- Publications
- 24 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
| Population | Group | Sample Size | Ref Allele | Alt Allele | Ref HMOZ | Alt HMOZ | HTRZ | HWEP |
|---|---|---|---|---|---|---|---|---|
| Total | Global | 189758 | G=0.998614 | A=0.001386 | 0.997892 | 0.000664 | 0.001444 | 32 |
| European | Sub | 168480 | G=0.998676 | A=0.001324 | 0.998006 | 0.000653 | 0.001341 | 32 |
| African | Sub | 5090 | G=0.9994 | A=0.0006 | 0.998821 | 0.0 | 0.001179 | 0 |
| African Others | Sub | 178 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| African American | Sub | 4912 | G=0.9994 | A=0.0006 | 0.998779 | 0.0 | 0.001221 | 0 |
| Asian | Sub | 4592 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| East Asian | Sub | 3166 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| Other Asian | Sub | 1426 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 1 | Sub | 416 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 2 | Sub | 1084 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| South Asian | Sub | 288 | G=0.983 | A=0.017 | 0.979167 | 0.013889 | 0.006944 | 32 |
| Other | Sub | 9808 | G=0.9967 | A=0.0033 | 0.994698 | 0.001223 | 0.004078 | 32 |
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").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD v4 - Exomes | Global | Study-wide | 1051813 | G=0.9985977 | A=0.0014023 |
| gnomAD v4 - Exomes | European | Sub | 882362 | G=0.999820 | A=0.000180 |
| gnomAD v4 - Exomes | South Asian | Sub | 54137 | G=0.98114 | A=0.01886 |
| gnomAD v4 - Exomes | American | Sub | 35192 | G=0.99997 | A=0.00003 |
| gnomAD v4 - Exomes | East Asian | Sub | 30205 | G=1.00000 | A=0.00000 |
| gnomAD v4 - Exomes | African | Sub | 26401 | G=0.99970 | A=0.00030 |
| gnomAD v4 - Exomes | Ashkenazi Jewish | Sub | 19381 | G=0.99453 | A=0.00547 |
| gnomAD v4 - Exomes | Middle Eastern | sub | 4135 | G=0.9565 | A=0.0435 |
| TopMed | Global | Study-wide | 264690 | G=0.999441 | A=0.000559 |
| Allele Frequency Aggregator | Total | Global | 189758 | G=0.998614 | A=0.001386 |
| Allele Frequency Aggregator | European | Sub | 168480 | G=0.998676 | A=0.001324 |
| Allele Frequency Aggregator | Other | Sub | 9808 | G=0.9967 | A=0.0033 |
| Allele Frequency Aggregator | African | Sub | 5090 | G=0.9994 | A=0.0006 |
| Allele Frequency Aggregator | Asian | Sub | 4592 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 1084 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 416 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 288 | G=0.983 | A=0.017 |
| gnomAD v4 - Genomes | Global | Study-wide | 109659 | G=0.999325 | A=0.000675 |
| gnomAD v4 - Genomes | European | Sub | 59114 | G=0.99981 | A=0.00019 |
| gnomAD v4 - Genomes | African | Sub | 30815 | G=0.99987 | A=0.00013 |
| gnomAD v4 - Genomes | American | Sub | 10658 | G=1.00000 | A=0.00000 |
| gnomAD v4 - Genomes | East Asian | Sub | 3528 | G=1.0000 | A=0.0000 |
| gnomAD v4 - Genomes | South Asian | Sub | 2677 | G=0.9851 | A=0.0149 |
| gnomAD v4 - Genomes | Ashkenazi Jewish | Sub | 2649 | G=0.9940 | A=0.0060 |
| gnomAD v4 - Genomes | Middle Eastern | sub | 218 | G=0.986 | A=0.014 |
| ExAC | Global | Study-wide | 87438 | G=0.99735 | A=0.00265 |
| ExAC | Europe | Sub | 52284 | G=0.99897 | A=0.00103 |
| ExAC | Asian | Sub | 16742 | G=0.99032 | A=0.00968 |
| ExAC | American | Sub | 9297 | G=0.9994 | A=0.0006 |
| ExAC | African | Sub | 8491 | G=0.9996 | A=0.0004 |
| ExAC | Other | Sub | 624 | G=0.989 | A=0.011 |
| 1000Genomes_30X | Global | Study-wide | 4805 | G=0.9992 | A=0.0008 |
| 1000Genomes_30X | African | Sub | 1328 | G=1.0000 | A=0.0000 |
| 1000Genomes_30X | Europe | Sub | 961 | G=1.000 | A=0.000 |
| 1000Genomes_30X | South Asian | Sub | 883 | G=0.995 | A=0.005 |
| 1000Genomes_30X | East Asian | Sub | 878 | G=1.000 | A=0.000 |
| 1000Genomes_30X | American | Sub | 755 | G=1.000 | A=0.000 |
| 1000Genomes | Global | Study-wide | 3775 | G=0.9992 | A=0.0008 |
| 1000Genomes | African | Sub | 1003 | G=1.0000 | A=0.0000 |
| 1000Genomes | Europe | Sub | 766 | G=1.000 | A=0.000 |
| 1000Genomes | East Asian | Sub | 764 | G=1.000 | A=0.000 |
| 1000Genomes | South Asian | Sub | 718 | G=0.996 | A=0.004 |
| 1000Genomes | American | Sub | 524 | G=1.000 | A=0.000 |
| UK 10K study - Twins | TWIN COHORT | Study-wide | 3708 | G=0.9997 | A=0.0003 |
| The Avon Longitudinal Study of Parents and Children | PARENT AND CHILD COHORT | Study-wide | 2889 | G=0.9993 | A=0.0007 |
| Qatari | Global | Study-wide | 108 | G=0.972 | A=0.028 |
| SGDP_PRJ | Global | Study-wide | 6 | G=0.3 | A=0.7 |
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 molecular consequences from Sequence Ontology. 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 > 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.
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr X | NC_000023.11:g.154534419G>A |
| GRCh37.p13 chr X fix patch HG1497_PATCH | NW_003871103.3:g.1968398G>A |
| G6PD RefSeqGene | NG_009015.2:g.18154C>T |
| LOC127898544 genomic region | NG_147855.1:g.511G>A |
| GRCh37.p13 chr X | NC_000023.10:g.153762634G>A |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| G6PD transcript variant 1 | NM_000402.4:c.653C>T | S [TCC] > F [TTC] | Coding Sequence Variant |
| glucose-6-phosphate 1-dehydrogenase isoform a | NP_000393.4:p.Ser218Phe | S (Ser) > F (Phe) | Missense Variant |
| G6PD transcript variant 3 | NM_001360016.2:c.563C>T | S [TCC] > F [TTC] | Coding Sequence Variant |
| glucose-6-phosphate 1-dehydrogenase isoform b | NP_001346945.1:p.Ser188Phe | S (Ser) > F (Phe) | Missense Variant |
| G6PD transcript variant 2 | NM_001042351.3:c.563C>T | S [TCC] > F [TTC] | Coding Sequence Variant |
| glucose-6-phosphate 1-dehydrogenase isoform b | NP_001035810.1:p.Ser188Phe | S (Ser) > F (Phe) | Missense Variant |
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
| ClinVar Accession | Disease Names | Clinical Significance |
|---|---|---|
| RCV000011086.13 | G6PD MEDITERRANEAN | Other |
| RCV000011087.13 | G6PD SASSARI | Other |
| RCV000011088.13 | G6PD CAGLIARI | Other |
| RCV000079409.60 | not provided | Pathogenic |
| RCV000179363.58 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency | Pathogenic-Likely-Pathogenic |
| RCV000445579.15 | G6PD deficiency | Pathogenic |
| RCV000477810.12 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency,Malaria, susceptibility to | Pathogenic |
| RCV000623137.11 | Inborn genetic diseases | Pathogenic |
| RCV001250219.9 | G6PD deficient hemolytic anemia | Pathogenic |
| RCV001265539.9 | Hemolytic anemia, G6PD deficient (favism) | Pathogenic |
| RCV001528124.12 | Malaria, susceptibility to | Pathogenic |
| RCV002305806.10 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency | Uncertain-Significance |
| RCV002305807.10 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency | Uncertain-Significance |
| RCV002305808.10 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency | Uncertain-Significance |
| RCV002305849.10 | Anemia, nonspherocytic hemolytic, due to G6PD deficiency | Likely-Pathogenic |
| RCV003925095.1 | G6PD-related disorder | Pathogenic |
| RCV004584350.1 | See cases | Likely-Pathogenic |
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name 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".
| Placement | G= | A |
|---|---|---|
| GRCh38.p14 chr X | NC_000023.11:g.154534419= | NC_000023.11:g.154534419G>A |
| GRCh37.p13 chr X fix patch HG1497_PATCH | NW_003871103.3:g.1968398= | NW_003871103.3:g.1968398G>A |
| G6PD RefSeqGene | NG_009015.2:g.18154= | NG_009015.2:g.18154C>T |
| G6PD transcript variant 1 | NM_000402.4:c.653= | NM_000402.4:c.653C>T |
| G6PD transcript variant 1 | NM_000402.3:c.653= | NM_000402.3:c.653C>T |
| G6PD transcript variant 2 | NM_001042351.3:c.563= | NM_001042351.3:c.563C>T |
| G6PD transcript variant 2 | NM_001042351.2:c.563= | NM_001042351.2:c.563C>T |
| G6PD transcript variant 2 | NM_001042351.1:c.563= | NM_001042351.1:c.563C>T |
| G6PD transcript variant 3 | NM_001360016.2:c.563= | NM_001360016.2:c.563C>T |
| G6PD transcript variant 1 | NM_001360016.1:c.563= | NM_001360016.1:c.563C>T |
| LOC127898544 genomic region | NG_147855.1:g.511= | NG_147855.1:g.511G>A |
| GRCh37.p13 chr X | NC_000023.10:g.153762634= | NC_000023.10:g.153762634G>A |
| glucose-6-phosphate 1-dehydrogenase isoform a | NP_000393.4:p.Ser218= | NP_000393.4:p.Ser218Phe |
| glucose-6-phosphate 1-dehydrogenase isoform b | NP_001035810.1:p.Ser188= | NP_001035810.1:p.Ser188Phe |
| glucose-6-phosphate 1-dehydrogenase isoform b | NP_001346945.1:p.Ser188= | NP_001346945.1:p.Ser188Phe |
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#.
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | HGBASE | ss7986035 | Mar 31, 2003 (113) |
| 2 | ILLUMINA | ss161109713 | Dec 01, 2009 (131) |
| 3 | OMICIA | ss244239881 | Aug 29, 2012 (137) |
| 4 | OMIM-CURATED-RECORDS | ss289479829 | Jan 06, 2011 (133) |
| 5 | NHLBI-ESP | ss342562463 | May 09, 2011 (134) |
| 6 | ILLUMINA | ss483026670 | Sep 11, 2015 (146) |
| 7 | EXOME_CHIP | ss491580924 | May 04, 2012 (137) |
| 8 | CLINSEQ_SNP | ss491955733 | May 04, 2012 (137) |
| 9 | ILLUMINA | ss780769153 | Sep 11, 2015 (146) |
| 10 | JMKIDD_LAB | ss1067612239 | Apr 09, 2015 (144) |
| 11 | 1000GENOMES | ss1556698389 | Apr 09, 2015 (144) |
| 12 | EVA_UK10K_ALSPAC | ss1641785217 | Apr 09, 2015 (144) |
| 13 | EVA_UK10K_TWINSUK | ss1684779250 | Apr 09, 2015 (144) |
| 14 | EVA_EXAC | ss1694662764 | Apr 09, 2015 (144) |
| 15 | ILLUMINA | ss1752801563 | Sep 11, 2015 (146) |
| 16 | ILLUMINA | ss1917720703 | Feb 17, 2016 (147) |
| 17 | WEILL_CORNELL_DGM | ss1939852047 | Feb 17, 2016 (147) |
| 18 | ILLUMINA | ss1945981456 | Feb 17, 2016 (147) |
| 19 | ILLUMINA | ss1958229233 | Feb 17, 2016 (147) |
| 20 | HUMAN_LONGEVITY | ss2321325374 | Dec 20, 2016 (150) |
| 21 | ILLUMINA | ss2711191347 | Oct 13, 2018 (152) |
| 22 | ILLUMINA | ss2711191348 | Oct 13, 2018 (152) |
| 23 | GNOMAD | ss2745624974 | Oct 13, 2018 (152) |
| 24 | GNOMAD | ss2746166213 | Oct 13, 2018 (152) |
| 25 | GNOMAD | ss2984756128 | Oct 13, 2018 (152) |
| 26 | AFFY | ss2985493622 | Oct 13, 2018 (152) |
| 27 | AFFY | ss2986139338 | Oct 13, 2018 (152) |
| 28 | ILLUMINA | ss3023047865 | Oct 13, 2018 (152) |
| 29 | ILLUMINA | ss3635263272 | Oct 13, 2018 (152) |
| 30 | ILLUMINA | ss3637012661 | Oct 13, 2018 (152) |
| 31 | ILLUMINA | ss3640970743 | Oct 13, 2018 (152) |
| 32 | ILLUMINA | ss3645020370 | Oct 13, 2018 (152) |
| 33 | ILLUMINA | ss3653606133 | Oct 13, 2018 (152) |
| 34 | ILLUMINA | ss3654261373 | Oct 13, 2018 (152) |
| 35 | ILLUMINA | ss3726710861 | Jul 14, 2019 (153) |
| 36 | ILLUMINA | ss3744602552 | Jul 14, 2019 (153) |
| 37 | ILLUMINA | ss3745563776 | Jul 14, 2019 (153) |
| 38 | ILLUMINA | ss3773055382 | Jul 14, 2019 (153) |
| 39 | EVA | ss3825516068 | Apr 27, 2020 (154) |
| 40 | SGDP_PRJ | ss3892536814 | Apr 27, 2020 (154) |
| 41 | FSA-LAB | ss3984446469 | Apr 27, 2021 (155) |
| 42 | EVA | ss3986888532 | Apr 27, 2021 (155) |
| 43 | EVA | ss6328867542 | Nov 02, 2024 (157) |
| 44 | GNOMAD | ss6473686649 | Nov 02, 2024 (157) |
| 45 | TOPMED | ss8141613124 | Nov 02, 2024 (157) |
| 46 | 1000G_HIGH_COVERAGE | ss8314364513 | Nov 02, 2024 (157) |
| 47 | HUGCELL_USP | ss8505716653 | Nov 02, 2024 (157) |
| 48 | EVA | ss8512474061 | Nov 02, 2024 (157) |
| 49 | 1000G_HIGH_COVERAGE | ss8623703387 | Nov 02, 2024 (157) |
| 50 | EVA | ss8848241663 | Nov 02, 2024 (157) |
| 51 | EVA | ss8979247984 | Nov 02, 2024 (157) |
| 52 | EVA | ss8979924772 | Nov 02, 2024 (157) |
| 53 | EVA | ss8982064787 | Nov 02, 2024 (157) |
| 54 | GNOMAD | ss10110230410 | Nov 02, 2024 (157) |
| 55 | 1000Genomes | NC_000023.10 - 153762634 | Oct 13, 2018 (152) |
| 56 | 1000Genomes_30X | NC_000023.11 - 154534419 | Nov 02, 2024 (157) |
| 57 | The Avon Longitudinal Study of Parents and Children | NC_000023.10 - 153762634 | Oct 13, 2018 (152) |
| 58 | ExAC | NC_000023.10 - 153762634 | Oct 13, 2018 (152) |
| 59 | gnomAD v4 - Exomes | NC_000023.11 - 154534419 | Nov 02, 2024 (157) |
| 60 | gnomAD v4 - Genomes | NC_000023.11 - 154534419 | Nov 02, 2024 (157) |
| 61 | Qatari | NC_000023.10 - 153762634 | Apr 27, 2020 (154) |
| 62 | SGDP_PRJ | NC_000023.10 - 153762634 | Apr 27, 2020 (154) |
| 63 | TopMed | NC_000023.11 - 154534419 | Apr 27, 2021 (155) |
| 64 | UK 10K study - Twins | NC_000023.10 - 153762634 | Oct 13, 2018 (152) |
| 65 | ALFA | NC_000023.11 - 154534419 | Nov 02, 2024 (157) |
| 66 | ClinVar | RCV000011086.13 | Nov 02, 2024 (157) |
| 67 | ClinVar | RCV000011087.13 | Nov 02, 2024 (157) |
| 68 | ClinVar | RCV000011088.13 | Nov 02, 2024 (157) |
| 69 | ClinVar | RCV000079409.60 | Nov 02, 2024 (157) |
| 70 | ClinVar | RCV000179363.58 | Nov 02, 2024 (157) |
| 71 | ClinVar | RCV000445579.15 | Nov 02, 2024 (157) |
| 72 | ClinVar | RCV000477810.12 | Nov 02, 2024 (157) |
| 73 | ClinVar | RCV000623137.11 | Nov 02, 2024 (157) |
| 74 | ClinVar | RCV001250219.9 | Nov 02, 2024 (157) |
| 75 | ClinVar | RCV001265539.9 | Nov 02, 2024 (157) |
| 76 | ClinVar | RCV001528124.12 | Nov 02, 2024 (157) |
| 77 | ClinVar | RCV002305806.10 | Nov 02, 2024 (157) |
| 78 | ClinVar | RCV002305807.10 | Nov 02, 2024 (157) |
| 79 | ClinVar | RCV002305808.10 | Nov 02, 2024 (157) |
| 80 | ClinVar | RCV002305849.10 | Nov 02, 2024 (157) |
| 81 | ClinVar | RCV003925095.1 | Nov 02, 2024 (157) |
| 82 | ClinVar | RCV004584350.1 | Nov 02, 2024 (157) |
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).
| Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
|---|---|---|---|
| ss491955733 | NC_000023.9:153415827:G:A | NC_000023.11:154534418:G:A | (self) |
| 84651606, 46612227, 10174611, 21893969, 44553794, 46612227, ss342562463, ss483026670, ss491580924, ss780769153, ss1067612239, ss1556698389, ss1641785217, ss1684779250, ss1694662764, ss1752801563, ss1917720703, ss1939852047, ss1945981456, ss1958229233, ss2711191347, ss2711191348, ss2745624974, ss2746166213, ss2984756128, ss2985493622, ss2986139338, ss3023047865, ss3635263272, ss3637012661, ss3640970743, ss3645020370, ss3653606133, ss3654261373, ss3744602552, ss3745563776, ss3773055382, ss3825516068, ss3892536814, ss3984446469, ss3986888532, ss6328867542, ss8512474061, ss8848241663, ss8979247984, ss8979924772, ss8982064787 | NC_000023.10:153762633:G:A | NC_000023.11:154534418:G:A | (self) |
| RCV000011086.13, RCV000011087.13, RCV000011088.13, RCV000079409.60, RCV000179363.58, RCV000445579.15, RCV000477810.12, RCV000623137.11, RCV001250219.9, RCV001265539.9, RCV001528124.12, RCV002305806.10, RCV002305807.10, RCV002305808.10, RCV002305849.10, RCV003925095.1, RCV004584350.1, 111229322, 69040187, 638030936, 705219481, 15617270547, ss244239881, ss289479829, ss2321325374, ss3726710861, ss6473686649, ss8141613124, ss8314364513, ss8505716653, ss8623703387, ss10110230410 | NC_000023.11:154534418:G:A | NC_000023.11:154534418:G:A | (self) |
| ss7986035, ss161109713 | NT_167198.1:4680571:G:A | NC_000023.11:154534418:G:A | (self) |
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
| PMID | Title | Author | Year | Journal |
|---|---|---|---|---|
| 1551674 | Molecular heterogeneity underlying the G6PD Mediterranean phenotype. | Corcoran CM et al. | 1992 | Human genetics |
| 1972698 | Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: evidence for a single origin of the common G6PD A- mutation. | Beutler E et al. | 1990 | Human genetics |
| 1978555 | Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East. | Kurdi-Haidar B et al. | 1990 | American journal of human genetics |
| 2503817 | G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation. | Vulliamy TJ et al. | 1989 | Nucleic acids research |
| 3393536 | Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia. | Vulliamy TJ et al. | 1988 | Proceedings of the National Academy of Sciences of the United States of America |
| 4974311 | A new structural variant of glucose-6-phosphate dehydrogenase with a high production rate (G6PD Hektoen). | Dern RJ et al. | 1969 | The Journal of laboratory and clinical medicine |
| 5305539 | Characterization of glucose-6-phosphate dehydrogenase variants. I. Occurrence of a G6PD Seattle-like variant in Sardinia and its interaction with the G6PD Mediterranean variant. | Lenzerini L et al. | 1969 | American journal of human genetics |
| 5369703 | Hereditary hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (Mediterranean type). | Benbassat J et al. | 1969 | Israel journal of medical sciences |
| 6698555 | G6PD Cagliari: a new low activity glucose 6-phosphate dehydrogenase variant characterized by enhanced intracellular lability. | Morelli A et al. | 1984 | Human genetics |
| 7203486 | Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia. | Testa U et al. | 1980 | Human genetics |
| 9342374 | Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia. | Kaplan M et al. | 1997 | Proceedings of the National Academy of Sciences of the United States of America |
| 11445808 | Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes. | Kaplan M et al. | 2001 | The Journal of pediatrics |
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The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.