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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.

rs9273493

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:32660470 (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
C=0.473241 (53851/113792, GnomAD)
C=0.46158 (12831/27798, 14KJPN)
T=0.44755 (7501/16760, 8.3KJPN) (+ 12 more)
T=0.44687 (7217/16150, ALFA)
T=0.4778 (3060/6404, 1000G_30x)
T=0.4585 (2296/5008, 1000G)
T=0.4225 (1893/4480, Estonian)
T=0.4266 (1250/2930, KOREAN)
T=0.461 (460/998, GoNL)
T=0.427 (256/600, NorthernSweden)
C=0.234 (125/534, MGP)
T=0.272 (123/452, SGDP_PRJ)
T=0.421 (91/216, Qatari)
T=0.360 (77/214, Vietnamese)
T=0.26 (11/42, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
HLA-DQB1-AS1 : Non Coding Transcript Variant
HLA-DQB1 : Intron Variant
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 16150 T=0.44687 A=0.00000, C=0.55313
European Sub 11712 T=0.42802 A=0.00000, C=0.57198
African Sub 2546 T=0.5613 A=0.0000, C=0.4387
African Others Sub 96 T=0.61 A=0.00, C=0.39
African American Sub 2450 T=0.5592 A=0.0000, C=0.4408
Asian Sub 112 T=0.429 A=0.000, C=0.571
East Asian Sub 86 T=0.38 A=0.00, C=0.62
Other Asian Sub 26 T=0.58 A=0.00, C=0.42
Latin American 1 Sub 154 T=0.448 A=0.000, C=0.552
Latin American 2 Sub 616 T=0.339 A=0.000, C=0.661
South Asian Sub 94 T=0.53 A=0.00, C=0.47
Other Sub 916 T=0.436 A=0.000, C=0.564


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
gnomAD - Genomes Global Study-wide 113792 T=0.526759 C=0.473241
gnomAD - Genomes European Sub 62912 T=0.50647 C=0.49353
gnomAD - Genomes African Sub 34704 T=0.57284 C=0.42716
gnomAD - Genomes American Sub 9274 T=0.5280 C=0.4720
gnomAD - Genomes Ashkenazi Jewish Sub 2738 T=0.4653 C=0.5347
gnomAD - Genomes East Asian Sub 2470 T=0.4680 C=0.5320
gnomAD - Genomes Other Sub 1694 T=0.5142 C=0.4858
14KJPN JAPANESE Study-wide 27798 T=0.53842 C=0.46158
8.3KJPN JAPANESE Study-wide 16760 T=0.44755 C=0.55245
Allele Frequency Aggregator Total Global 16150 T=0.44687 A=0.00000, C=0.55313
Allele Frequency Aggregator European Sub 11712 T=0.42802 A=0.00000, C=0.57198
Allele Frequency Aggregator African Sub 2546 T=0.5613 A=0.0000, C=0.4387
Allele Frequency Aggregator Other Sub 916 T=0.436 A=0.000, C=0.564
Allele Frequency Aggregator Latin American 2 Sub 616 T=0.339 A=0.000, C=0.661
Allele Frequency Aggregator Latin American 1 Sub 154 T=0.448 A=0.000, C=0.552
Allele Frequency Aggregator Asian Sub 112 T=0.429 A=0.000, C=0.571
Allele Frequency Aggregator South Asian Sub 94 T=0.53 A=0.00, C=0.47
1000Genomes_30x Global Study-wide 6404 T=0.4778 C=0.5222
1000Genomes_30x African Sub 1786 T=0.5162 C=0.4838
1000Genomes_30x Europe Sub 1266 T=0.4494 C=0.5506
1000Genomes_30x South Asian Sub 1202 T=0.5308 C=0.4692
1000Genomes_30x East Asian Sub 1170 T=0.4966 C=0.5034
1000Genomes_30x American Sub 980 T=0.357 C=0.643
1000Genomes Global Study-wide 5008 T=0.4585 C=0.5415
1000Genomes African Sub 1322 T=0.4962 C=0.5038
1000Genomes East Asian Sub 1008 T=0.4772 C=0.5228
1000Genomes Europe Sub 1006 T=0.4284 C=0.5716
1000Genomes South Asian Sub 978 T=0.525 C=0.475
1000Genomes American Sub 694 T=0.310 C=0.690
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4225 C=0.5775
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4266 C=0.5734, G=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.461 C=0.539
Northern Sweden ACPOP Study-wide 600 T=0.427 C=0.573
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.766 C=0.234
SGDP_PRJ Global Study-wide 452 T=0.272 C=0.728
Qatari Global Study-wide 216 T=0.421 C=0.579
A Vietnamese Genetic Variation Database Global Study-wide 214 T=0.360 C=0.640
Siberian Global Study-wide 42 T=0.26 C=0.74
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.32660470T>A
GRCh38.p14 chr 6 NC_000006.12:g.32660470T>C
GRCh38.p14 chr 6 NC_000006.12:g.32660470T>G
GRCh37.p13 chr 6 NC_000006.11:g.32628247T>A
GRCh37.p13 chr 6 NC_000006.11:g.32628247T>C
GRCh37.p13 chr 6 NC_000006.11:g.32628247T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4073413C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4073413C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4073413C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4073519C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4073519C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4073519C>G
HLA-DQB1 RefSeqGene NG_029922.1:g.11593G>A
HLA-DQB1 RefSeqGene NG_029922.1:g.11593G>T
HLA-DQB1 RefSeqGene NG_029922.1:g.11593G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3854377C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3854377C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3854377C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859973C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859973C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859973C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3901300C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3901300C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3901300C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906885C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906885C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906885C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057703C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057703C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057703C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4057001C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4057001C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4057001C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077922C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077922C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077922C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4083542C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4083542C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4083542C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956838C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956838C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956838C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3962423C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3962423C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3962423C>G
Gene: HLA-DQB1, major histocompatibility complex, class II, DQ beta 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
HLA-DQB1 transcript variant 2 NM_001243961.2:c.797-221A…

NM_001243961.2:c.797-221A>T

 		N/A Intron Variant
HLA-DQB1 transcript variant 1 NM_002123.5:c.773-221A>T N/A Intron Variant
Gene: HLA-DQB1-AS1, HLA-DQB1 antisense RNA 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
HLA-DQB1-AS1 transcript NR_133907.1:n.293T>A N/A Non Coding Transcript Variant
HLA-DQB1-AS1 transcript NR_133907.1:n.293T>C N/A Non Coding Transcript Variant
HLA-DQB1-AS1 transcript NR_133907.1:n.293T>G N/A Non Coding Transcript Variant
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.32660470= NC_000006.12:g.32660470T>A NC_000006.12:g.32660470T>C NC_000006.12:g.32660470T>G
GRCh37.p13 chr 6 NC_000006.11:g.32628247= NC_000006.11:g.32628247T>A NC_000006.11:g.32628247T>C NC_000006.11:g.32628247T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4073413C>T NT_113891.3:g.4073413C>A NT_113891.3:g.4073413= NT_113891.3:g.4073413C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4073519C>T NT_113891.2:g.4073519C>A NT_113891.2:g.4073519= NT_113891.2:g.4073519C>G
HLA-DQB1 RefSeqGene NG_029922.1:g.11593G>A NG_029922.1:g.11593G>T NG_029922.1:g.11593= NG_029922.1:g.11593G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3854377C>T NT_167248.2:g.3854377C>A NT_167248.2:g.3854377= NT_167248.2:g.3854377C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859973C>T NT_167248.1:g.3859973C>A NT_167248.1:g.3859973= NT_167248.1:g.3859973C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3901300C>T NT_167245.2:g.3901300C>A NT_167245.2:g.3901300= NT_167245.2:g.3901300C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906885C>T NT_167245.1:g.3906885C>A NT_167245.1:g.3906885= NT_167245.1:g.3906885C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057703C>T NT_167249.2:g.4057703C>A NT_167249.2:g.4057703= NT_167249.2:g.4057703C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4057001C>T NT_167249.1:g.4057001C>A NT_167249.1:g.4057001= NT_167249.1:g.4057001C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077922C>T NT_167246.2:g.4077922C>A NT_167246.2:g.4077922= NT_167246.2:g.4077922C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4083542C>T NT_167246.1:g.4083542C>A NT_167246.1:g.4083542= NT_167246.1:g.4083542C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956838C>T NT_167247.2:g.3956838C>A NT_167247.2:g.3956838= NT_167247.2:g.3956838C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3962423C>T NT_167247.1:g.3962423C>A NT_167247.1:g.3962423= NT_167247.1:g.3962423C>G
HLA-DQB1-AS1 transcript NR_133907.1:n.293= NR_133907.1:n.293T>A NR_133907.1:n.293T>C NR_133907.1:n.293T>G
HLA-DQB1 transcript variant 2 NM_001243961.1:c.797-221= NM_001243961.1:c.797-221A>T NM_001243961.1:c.797-221A>G NM_001243961.1:c.797-221A>C
HLA-DQB1 transcript variant 2 NM_001243961.2:c.797-221= NM_001243961.2:c.797-221A>T NM_001243961.2:c.797-221A>G NM_001243961.2:c.797-221A>C
HLA-DQB1 transcript variant 3 NM_001243962.1:c.773-222G>A NM_001243962.1:c.773-222G>T NM_001243962.1:c.773-222= NM_001243962.1:c.773-222G>C
HLA-DQB1 transcript variant 1 NM_002123.4:c.773-221= NM_002123.4:c.773-221A>T NM_002123.4:c.773-221A>G NM_002123.4:c.773-221A>C
HLA-DQB1 transcript variant 1 NM_002123.5:c.773-221= NM_002123.5:c.773-221A>T NM_002123.5:c.773-221A>G NM_002123.5:c.773-221A>C
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#.

53 SubSNP, 15 Frequency submissions
No Submitter Submission ID Date (Build)
1 SI_MHC_SNP ss12698460 Oct 31, 2003 (118)
2 UWGC ss50397104 Mar 15, 2006 (126)
3 BGI ss104299787 Feb 13, 2009 (130)
4 COMPLETE_GENOMICS ss162212987 Jul 04, 2010 (132)
5 COMPLETE_GENOMICS ss163366469 Jul 04, 2010 (132)
6 COMPLETE_GENOMICS ss166456229 Jul 04, 2010 (132)
7 BCM-HGSC-SUB ss207723282 Jul 04, 2010 (132)
8 1000GENOMES ss210642826 Jul 14, 2010 (132)
9 1000GENOMES ss211817737 Jul 14, 2010 (132)
10 1000GENOMES ss222316154 Jul 14, 2010 (132)
11 1000GENOMES ss233413408 Jul 14, 2010 (132)
12 1000GENOMES ss240480729 Jul 15, 2010 (132)
13 BL ss254211312 May 09, 2011 (134)
14 GMI ss278739440 May 04, 2012 (137)
15 PJP ss293830335 May 09, 2011 (134)
16 ILLUMINA ss536521917 Sep 08, 2015 (146)
17 DBMHC ss539209908 Oct 01, 2012 (137)
18 SSMP ss653050014 Apr 25, 2013 (138)
19 EVA-GONL ss982783733 Aug 21, 2014 (142)
20 1000GENOMES ss1319594367 Aug 21, 2014 (142)
21 EVA_MGP ss1711124014 Apr 01, 2015 (144)
22 HAMMER_LAB ss1804366297 Sep 08, 2015 (146)
23 WEILL_CORNELL_DGM ss1926040776 Feb 12, 2016 (147)
24 GENOMED ss1970363141 Jul 19, 2016 (147)
25 JJLAB ss2023654479 Sep 14, 2016 (149)
26 USC_VALOUEV ss2151829565 Dec 20, 2016 (150)
27 SYSTEMSBIOZJU ss2626314945 Nov 08, 2017 (151)
28 GRF ss2707423915 Nov 08, 2017 (151)
29 SWEGEN ss2998836756 Nov 08, 2017 (151)
30 BIOINF_KMB_FNS_UNIBA ss3025617649 Nov 08, 2017 (151)
31 ILLUMINA ss3629510782 Oct 12, 2018 (152)
32 URBANLAB ss3648319610 Oct 12, 2018 (152)
33 EGCUT_WGS ss3666727033 Jul 13, 2019 (153)
34 EVA_DECODE ss3716935857 Jul 13, 2019 (153)
35 ACPOP ss3733378616 Jul 13, 2019 (153)
36 EVA ss3764843826 Jul 13, 2019 (153)
37 KHV_HUMAN_GENOMES ss3807999511 Jul 13, 2019 (153)
38 EVA ss3829847586 Apr 26, 2020 (154)
39 EVA ss3838401270 Apr 26, 2020 (154)
40 EVA ss3843844722 Apr 26, 2020 (154)
41 SGDP_PRJ ss3864298116 Apr 26, 2020 (154)
42 KRGDB ss3911076115 Apr 26, 2020 (154)
43 EVA ss3986035114 Apr 26, 2021 (155)
44 TOMMO_GENOMICS ss5176905730 Apr 26, 2021 (155)
45 EVA ss5364775615 Oct 17, 2022 (156)
46 1000G_HIGH_COVERAGE ss5553644207 Oct 17, 2022 (156)
47 SANFORD_IMAGENETICS ss5640126832 Oct 17, 2022 (156)
48 TOMMO_GENOMICS ss5714775400 Oct 17, 2022 (156)
49 YY_MCH ss5807340213 Oct 17, 2022 (156)
50 EVA ss5842047832 Oct 17, 2022 (156)
51 EVA ss5855293865 Oct 17, 2022 (156)
52 EVA ss5968617147 Oct 17, 2022 (156)
53 EVA ss5980359392 Oct 17, 2022 (156)
54 1000Genomes NC_000006.11 - 32628247 Oct 12, 2018 (152)
55 1000Genomes_30x NC_000006.12 - 32660470 Oct 17, 2022 (156)
56 Genetic variation in the Estonian population NC_000006.11 - 32628247 Oct 12, 2018 (152)
57 gnomAD - Genomes NC_000006.12 - 32660470 Apr 26, 2021 (155)
58 Genome of the Netherlands Release 5 NC_000006.11 - 32628247 Apr 26, 2020 (154)
59 KOREAN population from KRGDB NC_000006.11 - 32628247 Apr 26, 2020 (154)
60 Medical Genome Project healthy controls from Spanish population NC_000006.11 - 32628247 Apr 26, 2020 (154)
61 Northern Sweden NC_000006.11 - 32628247 Jul 13, 2019 (153)
62 Qatari NC_000006.11 - 32628247 Apr 26, 2020 (154)
63 SGDP_PRJ NC_000006.11 - 32628247 Apr 26, 2020 (154)
64 Siberian NC_000006.11 - 32628247 Apr 26, 2020 (154)
65 8.3KJPN NC_000006.11 - 32628247 Apr 26, 2021 (155)
66 14KJPN NC_000006.12 - 32660470 Oct 17, 2022 (156)
67 A Vietnamese Genetic Variation Database NC_000006.11 - 32628247 Jul 13, 2019 (153)
68 ALFA NC_000006.12 - 32660470 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)
rs36058284 May 23, 2006 (127)
rs281864435 Jan 09, 2013 (136)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
7851773022 NC_000006.12:32660469:T:A NC_000006.12:32660469:T:A (self)
ss50397104, ss162212987, ss163366469, ss166456229, ss207723282, ss210642826, ss211817737, ss254211312, ss278739440, ss293830335 NC_000006.10:32736224:T:C NC_000006.12:32660469:T:C (self)
31363153, 12465281, 7778539, 18253509, 239774, 6663481, 8082706, 16315096, 4345919, 34875037, 3879530, ss222316154, ss233413408, ss240480729, ss536521917, ss653050014, ss982783733, ss1319594367, ss1711124014, ss1804366297, ss1926040776, ss1970363141, ss2023654479, ss2151829565, ss2626314945, ss2707423915, ss2998836756, ss3629510782, ss3666727033, ss3733378616, ss3764843826, ss3829847586, ss3838401270, ss3864298116, ss3911076115, ss3986035114, ss5176905730, ss5364775615, ss5640126832, ss5842047832, ss5968617147, ss5980359392 NC_000006.11:32628246:T:C NC_000006.12:32660469:T:C (self)
41170142, 221422625, 48612504, 7851773022, ss539209908, ss3025617649, ss3648319610, ss3716935857, ss3807999511, ss3843844722, ss5553644207, ss5714775400, ss5807340213, ss5855293865 NC_000006.12:32660469:T:C NC_000006.12:32660469:T:C (self)
ss12698460, ss104299787 NT_007592.15:32568246:T:C NC_000006.12:32660469:T:C (self)
18253509, ss3911076115 NC_000006.11:32628246:T:G NC_000006.12:32660469: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 rs9273493

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