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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs9276466

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:32748675 (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
T>A / T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.370233 (97997/264690, TOPMED)
T=0.386609 (53857/139306, GnomAD)
T=0.41487 (17506/42196, ALFA) (+ 18 more)
T=0.28233 (7978/28258, 14KJPN)
T=0.28276 (4739/16760, 8.3KJPN)
T=0.3159 (2023/6404, 1000G_30x)
T=0.3159 (1582/5008, 1000G)
T=0.4112 (1842/4480, Estonian)
T=0.4471 (1723/3854, ALSPAC)
T=0.4668 (1731/3708, TWINSUK)
T=0.2454 (719/2930, KOREAN)
T=0.3037 (342/1126, Daghestan)
T=0.491 (490/998, GoNL)
T=0.498 (299/600, NorthernSweden)
T=0.201 (100/498, SGDP_PRJ)
T=0.405 (133/328, HapMap)
T=0.426 (92/216, Qatari)
T=0.190 (41/216, Vietnamese)
T=0.24 (10/42, Siberian)
T=0.50 (20/40, GENOME_DK)
G=0.50 (20/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 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.

Release Version: 20230706150541
Population Group Sample Size Ref Allele Alt Allele
Total Global 42196 T=0.41487 G=0.58513
European Sub 29856 T=0.43258 G=0.56742
African Sub 6406 T=0.3592 G=0.6408
African Others Sub 216 T=0.394 G=0.606
African American Sub 6190 T=0.3580 G=0.6420
Asian Sub 434 T=0.214 G=0.786
East Asian Sub 370 T=0.216 G=0.784
Other Asian Sub 64 T=0.20 G=0.80
Latin American 1 Sub 212 T=0.373 G=0.627
Latin American 2 Sub 886 T=0.287 G=0.713
South Asian Sub 150 T=0.327 G=0.673
Other Sub 4252 T=0.4269 G=0.5731


Help

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
TopMed Global Study-wide 264690 T=0.370233 G=0.629767
gnomAD - Genomes Global Study-wide 139306 T=0.386609 G=0.613391
gnomAD - Genomes European Sub 75404 T=0.42910 G=0.57090
gnomAD - Genomes African Sub 41766 T=0.35426 G=0.64574
gnomAD - Genomes American Sub 13576 T=0.31644 G=0.68356
gnomAD - Genomes Ashkenazi Jewish Sub 3296 T=0.3541 G=0.6459
gnomAD - Genomes East Asian Sub 3118 T=0.1610 G=0.8390
gnomAD - Genomes Other Sub 2146 T=0.3448 G=0.6552
Allele Frequency Aggregator Total Global 42196 T=0.41487 G=0.58513
Allele Frequency Aggregator European Sub 29856 T=0.43258 G=0.56742
Allele Frequency Aggregator African Sub 6406 T=0.3592 G=0.6408
Allele Frequency Aggregator Other Sub 4252 T=0.4269 G=0.5731
Allele Frequency Aggregator Latin American 2 Sub 886 T=0.287 G=0.713
Allele Frequency Aggregator Asian Sub 434 T=0.214 G=0.786
Allele Frequency Aggregator Latin American 1 Sub 212 T=0.373 G=0.627
Allele Frequency Aggregator South Asian Sub 150 T=0.327 G=0.673
14KJPN JAPANESE Study-wide 28258 T=0.28233 G=0.71767
8.3KJPN JAPANESE Study-wide 16760 T=0.28276 G=0.71724
1000Genomes_30x Global Study-wide 6404 T=0.3159 G=0.6841
1000Genomes_30x African Sub 1786 T=0.3600 G=0.6400
1000Genomes_30x Europe Sub 1266 T=0.3934 G=0.6066
1000Genomes_30x South Asian Sub 1202 T=0.3261 G=0.6739
1000Genomes_30x East Asian Sub 1170 T=0.1812 G=0.8188
1000Genomes_30x American Sub 980 T=0.284 G=0.716
1000Genomes Global Study-wide 5008 T=0.3159 G=0.6841
1000Genomes African Sub 1322 T=0.3585 G=0.6415
1000Genomes East Asian Sub 1008 T=0.1954 G=0.8046
1000Genomes Europe Sub 1006 T=0.3867 G=0.6133
1000Genomes South Asian Sub 978 T=0.331 G=0.669
1000Genomes American Sub 694 T=0.285 G=0.715
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4112 G=0.5888
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.4471 G=0.5529
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.4668 G=0.5332
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.2454 A=0.0000, C=0.0000, G=0.7546
Genome-wide autozygosity in Daghestan Global Study-wide 1126 T=0.3037 G=0.6963
Genome-wide autozygosity in Daghestan Daghestan Sub 618 T=0.267 G=0.733
Genome-wide autozygosity in Daghestan Near_East Sub 144 T=0.285 G=0.715
Genome-wide autozygosity in Daghestan Central Asia Sub 122 T=0.361 G=0.639
Genome-wide autozygosity in Daghestan Europe Sub 108 T=0.398 G=0.602
Genome-wide autozygosity in Daghestan South Asian Sub 98 T=0.42 G=0.58
Genome-wide autozygosity in Daghestan Caucasus Sub 36 T=0.22 G=0.78
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.491 G=0.509
Northern Sweden ACPOP Study-wide 600 T=0.498 G=0.502
SGDP_PRJ Global Study-wide 498 T=0.201 G=0.799
HapMap Global Study-wide 328 T=0.405 G=0.595
HapMap African Sub 120 T=0.367 G=0.633
HapMap American Sub 120 T=0.517 G=0.483
HapMap Asian Sub 88 T=0.31 G=0.69
Qatari Global Study-wide 216 T=0.426 G=0.574
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.190 G=0.810
Siberian Global Study-wide 42 T=0.24 G=0.76
The Danish reference pan genome Danish Study-wide 40 T=0.50 G=0.50
Help

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.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 6 NC_000006.12:g.32748675T>A
GRCh38.p14 chr 6 NC_000006.12:g.32748675T>C
GRCh38.p14 chr 6 NC_000006.12:g.32748675T>G
GRCh37.p13 chr 6 NC_000006.11:g.32716452T>A
GRCh37.p13 chr 6 NC_000006.11:g.32716452T>C
GRCh37.p13 chr 6 NC_000006.11:g.32716452T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4162249T>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4162249T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4162249T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4162355T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4162355T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4162355T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3942963G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3942963G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3942963G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3948559G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3948559G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3948559G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3993433G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3993433G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3993433G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3999018G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3999018G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3999018G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4148823T>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4148823T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4148823T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4148121T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4148121T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4148121T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4168014G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4168014G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4168014G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4173634G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4173634G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4173634G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.4048052G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.4048052G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.4048052G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.4053637G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.4053637G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.4053637G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.4054815T>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.4054815T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.4054815T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.4004731T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.4004731T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.4004731T>G
Help

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.

Not Reported in ClinVar
Help

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 T= A C G
GRCh38.p14 chr 6 NC_000006.12:g.32748675= NC_000006.12:g.32748675T>A NC_000006.12:g.32748675T>C NC_000006.12:g.32748675T>G
GRCh37.p13 chr 6 NC_000006.11:g.32716452= NC_000006.11:g.32716452T>A NC_000006.11:g.32716452T>C NC_000006.11:g.32716452T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4162249= NT_113891.3:g.4162249T>A NT_113891.3:g.4162249T>C NT_113891.3:g.4162249T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4162355= NT_113891.2:g.4162355T>A NT_113891.2:g.4162355T>C NT_113891.2:g.4162355T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3942963G>T NT_167248.2:g.3942963G>A NT_167248.2:g.3942963G>C NT_167248.2:g.3942963=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3948559G>T NT_167248.1:g.3948559G>A NT_167248.1:g.3948559G>C NT_167248.1:g.3948559=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3993433G>T NT_167245.2:g.3993433G>A NT_167245.2:g.3993433G>C NT_167245.2:g.3993433=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3999018G>T NT_167245.1:g.3999018G>A NT_167245.1:g.3999018G>C NT_167245.1:g.3999018=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4148823= NT_167249.2:g.4148823T>A NT_167249.2:g.4148823T>C NT_167249.2:g.4148823T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4148121= NT_167249.1:g.4148121T>A NT_167249.1:g.4148121T>C NT_167249.1:g.4148121T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4168014G>T NT_167246.2:g.4168014G>A NT_167246.2:g.4168014G>C NT_167246.2:g.4168014=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4173634G>T NT_167246.1:g.4173634G>A NT_167246.1:g.4173634G>C NT_167246.1:g.4173634=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.4048052G>T NT_167247.2:g.4048052G>A NT_167247.2:g.4048052G>C NT_167247.2:g.4048052=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.4053637G>T NT_167247.1:g.4053637G>A NT_167247.1:g.4053637G>C NT_167247.1:g.4053637=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.4054815= NT_167244.2:g.4054815T>A NT_167244.2:g.4054815T>C NT_167244.2:g.4054815T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.4004731= NT_167244.1:g.4004731T>A NT_167244.1:g.4004731T>C NT_167244.1:g.4004731T>G
Help

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#.

82 SubSNP, 20 Frequency submissions
No Submitter Submission ID Date (Build)
1 SI_MHC_SNP ss12701595 Oct 31, 2003 (118)
2 CSHL-HAPMAP ss17113308 Feb 27, 2004 (120)
3 ABI ss44698855 Mar 15, 2006 (126)
4 HGSV ss80336619 Dec 15, 2007 (130)
5 HGSV ss83699513 Dec 15, 2007 (130)
6 HUMANGENOME_JCVI ss98488262 Feb 06, 2009 (130)
7 BGI ss105991952 Feb 06, 2009 (130)
8 1000GENOMES ss109922495 Feb 13, 2009 (137)
9 1000GENOMES ss114168263 Jan 25, 2009 (137)
10 ILLUMINA-UK ss116405603 Feb 14, 2009 (130)
11 ENSEMBL ss133673118 Dec 01, 2009 (131)
12 ENSEMBL ss144246429 Dec 01, 2009 (131)
13 GMI ss156771479 Dec 01, 2009 (131)
14 ILLUMINA ss160971212 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss162219717 Jul 04, 2010 (132)
16 COMPLETE_GENOMICS ss163372217 Jul 04, 2010 (132)
17 COMPLETE_GENOMICS ss166464373 Jul 04, 2010 (132)
18 BUSHMAN ss201652106 Jul 04, 2010 (132)
19 1000GENOMES ss222319721 Jul 14, 2010 (137)
20 1000GENOMES ss233417055 Jul 14, 2010 (137)
21 1000GENOMES ss240483917 Jul 15, 2010 (137)
22 BL ss254216464 May 09, 2011 (137)
23 GMI ss278742671 May 04, 2012 (137)
24 GMI ss285381590 Apr 25, 2013 (138)
25 PJP ss293831820 May 09, 2011 (137)
26 ILLUMINA ss482842302 Sep 08, 2015 (146)
27 ILLUMINA ss537579878 Sep 08, 2015 (146)
28 TISHKOFF ss559121435 Apr 25, 2013 (138)
29 SSMP ss653053431 Apr 25, 2013 (138)
30 ILLUMINA ss778715423 Aug 21, 2014 (142)
31 ILLUMINA ss834174693 Aug 21, 2014 (142)
32 EVA-GONL ss982787602 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1073513288 Aug 21, 2014 (142)
34 1000GENOMES ss1319600135 Aug 21, 2014 (142)
35 HAMMER_LAB ss1397451841 Sep 08, 2015 (146)
36 EVA_GENOME_DK ss1581615747 Apr 01, 2015 (144)
37 EVA_DECODE ss1592321272 Apr 01, 2015 (144)
38 EVA_UK10K_ALSPAC ss1615293048 Apr 01, 2015 (144)
39 EVA_UK10K_TWINSUK ss1658287081 Apr 01, 2015 (144)
40 HAMMER_LAB ss1804368468 Sep 08, 2015 (146)
41 WEILL_CORNELL_DGM ss1926045510 Feb 12, 2016 (147)
42 GENOMED ss1970365036 Jul 19, 2016 (147)
43 JJLAB ss2023658072 Sep 14, 2016 (149)
44 USC_VALOUEV ss2151833987 Dec 20, 2016 (150)
45 HUMAN_LONGEVITY ss2282995184 Dec 20, 2016 (150)
46 SYSTEMSBIOZJU ss2626317040 Nov 08, 2017 (151)
47 ILLUMINA ss2634433880 Nov 08, 2017 (151)
48 GRF ss2707428856 Nov 08, 2017 (151)
49 SWEGEN ss2998843093 Nov 08, 2017 (151)
50 BIOINF_KMB_FNS_UNIBA ss3025620535 Nov 08, 2017 (151)
51 ILLUMINA ss3629512110 Oct 12, 2018 (152)
52 ILLUMINA ss3632351952 Oct 12, 2018 (152)
53 ILLUMINA ss3636781793 Oct 12, 2018 (152)
54 URBANLAB ss3648322984 Oct 12, 2018 (152)
55 EGCUT_WGS ss3666730116 Jul 13, 2019 (153)
56 EVA_DECODE ss3716941191 Jul 13, 2019 (153)
57 ACPOP ss3733383143 Jul 13, 2019 (153)
58 EVA ss3764847969 Jul 13, 2019 (153)
59 KHV_HUMAN_GENOMES ss3808004367 Jul 13, 2019 (153)
60 EVA ss3829851958 Apr 26, 2020 (154)
61 EVA ss3838403796 Apr 26, 2020 (154)
62 EVA ss3843847800 Apr 26, 2020 (154)
63 SGDP_PRJ ss3864304338 Apr 26, 2020 (154)
64 KRGDB ss3911082399 Apr 26, 2020 (154)
65 VINODS ss4025173432 Apr 26, 2021 (155)
66 VINODS ss4025196086 Apr 26, 2021 (155)
67 VINODS ss4025294769 Apr 26, 2021 (155)
68 TOPMED ss4698594008 Apr 26, 2021 (155)
69 TOMMO_GENOMICS ss5176914077 Apr 26, 2021 (155)
70 1000G_HIGH_COVERAGE ss5267975549 Oct 13, 2022 (156)
71 EVA ss5315144950 Oct 13, 2022 (156)
72 EVA ss5364781087 Oct 13, 2022 (156)
73 HUGCELL_USP ss5465696177 Oct 13, 2022 (156)
74 EVA ss5508439059 Oct 13, 2022 (156)
75 1000G_HIGH_COVERAGE ss5553651096 Oct 13, 2022 (156)
76 SANFORD_IMAGENETICS ss5640132906 Oct 13, 2022 (156)
77 TOMMO_GENOMICS ss5714785148 Oct 13, 2022 (156)
78 YY_MCH ss5807345947 Oct 13, 2022 (156)
79 EVA ss5842051967 Oct 13, 2022 (156)
80 EVA ss5855297057 Oct 13, 2022 (156)
81 EVA ss5883280374 Oct 13, 2022 (156)
82 EVA ss5968621779 Oct 13, 2022 (156)
83 1000Genomes NC_000006.11 - 32716452 Oct 12, 2018 (152)
84 1000Genomes_30x NC_000006.12 - 32748675 Oct 13, 2022 (156)
85 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 32716452 Oct 12, 2018 (152)
86 Genome-wide autozygosity in Daghestan NC_000006.10 - 32824430 Apr 26, 2020 (154)
87 Genetic variation in the Estonian population NC_000006.11 - 32716452 Oct 12, 2018 (152)
88 The Danish reference pan genome NC_000006.11 - 32716452 Apr 26, 2020 (154)
89 gnomAD - Genomes NC_000006.12 - 32748675 Apr 26, 2021 (155)
90 Genome of the Netherlands Release 5 NC_000006.11 - 32716452 Apr 26, 2020 (154)
91 HapMap NC_000006.12 - 32748675 Apr 26, 2020 (154)
92 KOREAN population from KRGDB NC_000006.11 - 32716452 Apr 26, 2020 (154)
93 Northern Sweden NC_000006.11 - 32716452 Jul 13, 2019 (153)
94 Qatari NC_000006.11 - 32716452 Apr 26, 2020 (154)
95 SGDP_PRJ NC_000006.11 - 32716452 Apr 26, 2020 (154)
96 Siberian NC_000006.11 - 32716452 Apr 26, 2020 (154)
97 8.3KJPN NC_000006.11 - 32716452 Apr 26, 2021 (155)
98 14KJPN NC_000006.12 - 32748675 Oct 13, 2022 (156)
99 TopMed NC_000006.12 - 32748675 Apr 26, 2021 (155)
100 UK 10K study - Twins NC_000006.11 - 32716452 Oct 12, 2018 (152)
101 A Vietnamese Genetic Variation Database NC_000006.11 - 32716452 Jul 13, 2019 (153)
102 ALFA NC_000006.12 - 32748675 Apr 26, 2021 (155)
Help

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).

Associated ID History Updated (Build)
rs60788839 May 26, 2008 (130)
rs115404818 May 04, 2012 (137)
rs117178334 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
18259793, ss3911082399 NC_000006.11:32716451:T:A NC_000006.12:32748674:T:A (self)
18259793, ss3911082399 NC_000006.11:32716451:T:C NC_000006.12:32748674:T:C (self)
ss80336619, ss83699513 NC_000006.9:32824429:T:G NC_000006.12:32748674:T:G (self)
426489, ss12701595, ss109922495, ss114168263, ss116405603, ss160971212, ss162219717, ss163372217, ss166464373, ss201652106, ss254216464, ss278742671, ss285381590, ss293831820, ss1397451841, ss1592321272 NC_000006.10:32824429:T:G NC_000006.12:32748674:T:G (self)
31369000, 17484698, 12468364, 7780686, 7781996, 18259793, 6668008, 8087440, 16321318, 4350341, 34883384, 17484698, 3880847, ss222319721, ss233417055, ss240483917, ss482842302, ss537579878, ss559121435, ss653053431, ss778715423, ss834174693, ss982787602, ss1073513288, ss1319600135, ss1581615747, ss1615293048, ss1658287081, ss1804368468, ss1926045510, ss1970365036, ss2023658072, ss2151833987, ss2626317040, ss2634433880, ss2707428856, ss2998843093, ss3629512110, ss3632351952, ss3636781793, ss3666730116, ss3733383143, ss3764847969, ss3829851958, ss3838403796, ss3864304338, ss3911082399, ss5176914077, ss5315144950, ss5364781087, ss5508439059, ss5640132906, ss5842051967, ss5968621779 NC_000006.11:32716451:T:G NC_000006.12:32748674:T:G (self)
41177031, 221441796, 3103212, 48622252, 535971566, 15395487705, ss2282995184, ss3025620535, ss3648322984, ss3716941191, ss3808004367, ss3843847800, ss4698594008, ss5267975549, ss5465696177, ss5553651096, ss5714785148, ss5807345947, ss5855297057, ss5883280374 NC_000006.12:32748674:T:G NC_000006.12:32748674:T:G (self)
ss17113308 NT_007592.13:23513733:G:G NC_000006.12:32748674:T:G (self)
ss44698855, ss98488262, ss105991952, ss133673118, ss144246429, ss156771479 NT_007592.15:32656451:T:G NC_000006.12:32748674:T:G (self)
ss4025196086 NT_113891.3:4162248:T:G NC_000006.12:32748674:T:G (self)
ss4025173432 NT_167244.2:4054814:T:G NC_000006.12:32748674:T:G (self)
ss4025294769 NT_167249.2:4148822:T:G NC_000006.12:32748674:T:G (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs9276466

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top▲ Help

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.

Software version is: 2.0.1.post761+d5e8e07