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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.

rs9273444

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:32659858 (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=0.415698 (110031/264690, TOPMED)
T=0.433449 (60089/138630, GnomAD)
T=0.41452 (7677/18520, ALFA) (+ 8 more)
T=0.4343 (2781/6404, 1000G_30x)
T=0.4489 (2248/5008, 1000G)
T=0.4210 (1886/4480, Estonian)
T=0.4263 (1249/2930, KOREAN)
T=0.425 (255/600, NorthernSweden)
T=0.272 (123/452, SGDP_PRJ)
T=0.417 (90/216, Qatari)
T=0.26 (11/42, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
HLA-DQB1 : 3 Prime UTR Variant
HLA-DQB1-AS1 : 2KB Upstream 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 18520 T=0.41452 G=0.58548
European Sub 14152 T=0.40298 G=0.59702
African Sub 2898 T=0.4993 G=0.5007
African Others Sub 114 T=0.544 G=0.456
African American Sub 2784 T=0.4975 G=0.5025
Asian Sub 112 T=0.384 G=0.616
East Asian Sub 86 T=0.37 G=0.63
Other Asian Sub 26 T=0.42 G=0.58
Latin American 1 Sub 146 T=0.418 G=0.582
Latin American 2 Sub 610 T=0.279 G=0.721
South Asian Sub 98 T=0.50 G=0.50
Other Sub 504 T=0.405 G=0.595


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=0.415698 G=0.584302
gnomAD - Genomes Global Study-wide 138630 T=0.433449 G=0.566551
gnomAD - Genomes European Sub 75244 T=0.42466 G=0.57534
gnomAD - Genomes African Sub 41350 T=0.48595 G=0.51405
gnomAD - Genomes American Sub 13504 T=0.35338 G=0.64662
gnomAD - Genomes Ashkenazi Jewish Sub 3310 T=0.3752 G=0.6248
gnomAD - Genomes East Asian Sub 3106 T=0.3738 G=0.6262
gnomAD - Genomes Other Sub 2116 T=0.4097 G=0.5903
Allele Frequency Aggregator Total Global 18520 T=0.41452 G=0.58548
Allele Frequency Aggregator European Sub 14152 T=0.40298 G=0.59702
Allele Frequency Aggregator African Sub 2898 T=0.4993 G=0.5007
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.279 G=0.721
Allele Frequency Aggregator Other Sub 504 T=0.405 G=0.595
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.418 G=0.582
Allele Frequency Aggregator Asian Sub 112 T=0.384 G=0.616
Allele Frequency Aggregator South Asian Sub 98 T=0.50 G=0.50
1000Genomes_30x Global Study-wide 6404 T=0.4343 G=0.5657
1000Genomes_30x African Sub 1786 T=0.4787 G=0.5213
1000Genomes_30x Europe Sub 1266 T=0.4036 G=0.5964
1000Genomes_30x South Asian Sub 1202 T=0.5033 G=0.4967
1000Genomes_30x East Asian Sub 1170 T=0.4513 G=0.5487
1000Genomes_30x American Sub 980 T=0.288 G=0.712
1000Genomes Global Study-wide 5008 T=0.4489 G=0.5511
1000Genomes African Sub 1322 T=0.4924 G=0.5076
1000Genomes East Asian Sub 1008 T=0.4692 G=0.5308
1000Genomes Europe Sub 1006 T=0.4115 G=0.5885
1000Genomes South Asian Sub 978 T=0.516 G=0.484
1000Genomes American Sub 694 T=0.295 G=0.705
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4210 G=0.5790
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.4263 A=0.0000, G=0.5737
Northern Sweden ACPOP Study-wide 600 T=0.425 G=0.575
SGDP_PRJ Global Study-wide 452 T=0.272 G=0.728
Qatari Global Study-wide 216 T=0.417 G=0.583
Siberian Global Study-wide 42 T=0.26 G=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.32659858T>A
GRCh38.p14 chr 6 NC_000006.12:g.32659858T>C
GRCh38.p14 chr 6 NC_000006.12:g.32659858T>G
GRCh37.p13 chr 6 NC_000006.11:g.32627635T>A
GRCh37.p13 chr 6 NC_000006.11:g.32627635T>C
GRCh37.p13 chr 6 NC_000006.11:g.32627635T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4072799G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4072799G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4072799G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4072905G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4072905G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4072905G>C
HLA-DQB1 RefSeqGene NG_029922.1:g.12207C>A
HLA-DQB1 RefSeqGene NG_029922.1:g.12207C>T
HLA-DQB1 RefSeqGene NG_029922.1:g.12207C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3853763G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3853763G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3853763G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859359G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859359G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859359G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3900687G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3900687G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3900687G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906272G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906272G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906272G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057089G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057089G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057089G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4056387G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4056387G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4056387G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077308G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077308G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077308G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4082928G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4082928G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4082928G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956225G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956225G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956225G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3961810G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3961810G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3961810G>C
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.*378= N/A 3 Prime UTR Variant
HLA-DQB1 transcript variant 1 NM_002123.5:c.*378= N/A 3 Prime UTR Variant
Gene: HLA-DQB1-AS1, HLA-DQB1 antisense RNA 1 (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
HLA-DQB1-AS1 transcript NR_133907.1:n. N/A Upstream 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.32659858= NC_000006.12:g.32659858T>A NC_000006.12:g.32659858T>C NC_000006.12:g.32659858T>G
GRCh37.p13 chr 6 NC_000006.11:g.32627635= NC_000006.11:g.32627635T>A NC_000006.11:g.32627635T>C NC_000006.11:g.32627635T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.4072799G>T NT_113891.3:g.4072799G>A NT_113891.3:g.4072799G>C NT_113891.3:g.4072799=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.4072905G>T NT_113891.2:g.4072905G>A NT_113891.2:g.4072905G>C NT_113891.2:g.4072905=
HLA-DQB1 RefSeqGene NG_029922.1:g.12207C>A NG_029922.1:g.12207C>T NG_029922.1:g.12207C>G NG_029922.1:g.12207=
HLA-DQB1 transcript variant 1 NM_002123.5:c.*378= NM_002123.5:c.*378A>T NM_002123.5:c.*378A>G NM_002123.5:c.*378A>C
HLA-DQB1 transcript variant 1 NM_002123.4:c.*378= NM_002123.4:c.*378A>T NM_002123.4:c.*378A>G NM_002123.4:c.*378A>C
HLA-DQB1 transcript variant 2 NM_001243961.2:c.*378= NM_001243961.2:c.*378A>T NM_001243961.2:c.*378A>G NM_001243961.2:c.*378A>C
HLA-DQB1 transcript variant 2 NM_001243961.1:c.*378= NM_001243961.1:c.*378A>T NM_001243961.1:c.*378A>G NM_001243961.1:c.*378A>C
HLA-DQB1 transcript variant 3 NM_001243962.1:c.*379C>A NM_001243962.1:c.*379C>T NM_001243962.1:c.*379C>G NM_001243962.1:c.*379=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.3853763G>T NT_167248.2:g.3853763G>A NT_167248.2:g.3853763G>C NT_167248.2:g.3853763=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.3859359G>T NT_167248.1:g.3859359G>A NT_167248.1:g.3859359G>C NT_167248.1:g.3859359=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.3900687G>T NT_167245.2:g.3900687G>A NT_167245.2:g.3900687G>C NT_167245.2:g.3900687=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.3906272G>T NT_167245.1:g.3906272G>A NT_167245.1:g.3906272G>C NT_167245.1:g.3906272=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.4057089G>T NT_167249.2:g.4057089G>A NT_167249.2:g.4057089G>C NT_167249.2:g.4057089=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.4056387G>T NT_167249.1:g.4056387G>A NT_167249.1:g.4056387G>C NT_167249.1:g.4056387=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.4077308G>T NT_167246.2:g.4077308G>A NT_167246.2:g.4077308G>C NT_167246.2:g.4077308=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.4082928G>T NT_167246.1:g.4082928G>A NT_167246.1:g.4082928G>C NT_167246.1:g.4082928=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.3956225G>T NT_167247.2:g.3956225G>A NT_167247.2:g.3956225G>C NT_167247.2:g.3956225=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.3961810G>T NT_167247.1:g.3961810G>A NT_167247.1:g.3961810G>C NT_167247.1:g.3961810=
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#.

60 SubSNP, 15 Frequency submissions
No Submitter Submission ID Date (Build)
1 SI_MHC_SNP ss12698411 Oct 31, 2003 (118)
2 UWGC ss50397212 Mar 15, 2006 (126)
3 SI_EXO ss69378164 May 18, 2007 (127)
4 BGI ss104299768 Dec 01, 2009 (137)
5 1000GENOMES ss109918326 Feb 13, 2009 (130)
6 1000GENOMES ss114162527 Jan 25, 2009 (130)
7 GMI ss156765794 Dec 01, 2009 (137)
8 COMPLETE_GENOMICS ss162212891 Jul 04, 2010 (132)
9 COMPLETE_GENOMICS ss163366321 Jul 04, 2010 (132)
10 COMPLETE_GENOMICS ss166456134 Jul 04, 2010 (132)
11 BUSHMAN ss201646732 Jul 04, 2010 (132)
12 BCM-HGSC-SUB ss207767858 Jul 04, 2010 (132)
13 GMI ss278739408 May 04, 2012 (137)
14 GMI ss285379614 Apr 25, 2013 (138)
15 PJP ss293830314 May 09, 2011 (134)
16 SSMP ss653049963 Apr 25, 2013 (138)
17 1000GENOMES ss1319594294 Aug 21, 2014 (142)
18 WEILL_CORNELL_DGM ss1926040704 Feb 12, 2016 (147)
19 GENOMED ss1970363127 Jul 19, 2016 (147)
20 JJLAB ss2023654414 Sep 14, 2016 (149)
21 USC_VALOUEV ss2151829495 Dec 20, 2016 (150)
22 SYSTEMSBIOZJU ss2626314914 Nov 08, 2017 (151)
23 GRF ss2707423842 Nov 08, 2017 (151)
24 SWEGEN ss2998836666 Nov 08, 2017 (151)
25 BIOINF_KMB_FNS_UNIBA ss3025617599 Nov 08, 2017 (151)
26 OMUKHERJEE_ADBS ss3646336462 Oct 12, 2018 (152)
27 URBANLAB ss3648319559 Oct 12, 2018 (152)
28 EGCUT_WGS ss3666726948 Jul 13, 2019 (153)
29 EVA_DECODE ss3716935765 Jul 13, 2019 (153)
30 ACPOP ss3733378535 Jul 13, 2019 (153)
31 PACBIO ss3785435412 Jul 13, 2019 (153)
32 PACBIO ss3790793080 Jul 13, 2019 (153)
33 PACBIO ss3795671436 Jul 13, 2019 (153)
34 KHV_HUMAN_GENOMES ss3807999442 Jul 13, 2019 (153)
35 EVA ss3829847515 Apr 26, 2020 (154)
36 EVA ss3838401227 Apr 26, 2020 (154)
37 EVA ss3843844657 Apr 26, 2020 (154)
38 SGDP_PRJ ss3864298033 Apr 26, 2020 (154)
39 KRGDB ss3911076036 Apr 26, 2020 (154)
40 EVA ss3986035071 Apr 26, 2021 (155)
41 VINODS ss4025194438 Apr 26, 2021 (155)
42 VINODS ss4025213960 Apr 26, 2021 (155)
43 VINODS ss4025234842 Apr 26, 2021 (155)
44 VINODS ss4025251399 Apr 26, 2021 (155)
45 VINODS ss4025272272 Apr 26, 2021 (155)
46 VINODS ss4025293297 Apr 26, 2021 (155)
47 TOPMED ss4698579038 Apr 26, 2021 (155)
48 TOMMO_GENOMICS ss5176905631 Apr 26, 2021 (155)
49 TOMMO_GENOMICS ss5176905632 Apr 26, 2021 (155)
50 1000G_HIGH_COVERAGE ss5267969975 Oct 17, 2022 (156)
51 EVA ss5364775554 Oct 17, 2022 (156)
52 EVA ss5508436542 Oct 17, 2022 (156)
53 1000G_HIGH_COVERAGE ss5553644118 Oct 17, 2022 (156)
54 SANFORD_IMAGENETICS ss5640126747 Oct 17, 2022 (156)
55 TOMMO_GENOMICS ss5714775296 Oct 17, 2022 (156)
56 TOMMO_GENOMICS ss5714775297 Oct 17, 2022 (156)
57 YY_MCH ss5807340133 Oct 17, 2022 (156)
58 EVA ss5842047778 Oct 17, 2022 (156)
59 EVA ss5883274344 Oct 17, 2022 (156)
60 EVA ss5980359353 Oct 17, 2022 (156)
61 1000Genomes NC_000006.11 - 32627635 Oct 12, 2018 (152)
62 1000Genomes_30x NC_000006.12 - 32659858 Oct 17, 2022 (156)
63 Genetic variation in the Estonian population NC_000006.11 - 32627635 Oct 12, 2018 (152)
64 gnomAD - Genomes NC_000006.12 - 32659858 Apr 26, 2021 (155)
65 KOREAN population from KRGDB NC_000006.11 - 32627635 Apr 26, 2020 (154)
66 Northern Sweden NC_000006.11 - 32627635 Jul 13, 2019 (153)
67 Qatari NC_000006.11 - 32627635 Apr 26, 2020 (154)
68 SGDP_PRJ NC_000006.11 - 32627635 Apr 26, 2020 (154)
69 Siberian NC_000006.11 - 32627635 Apr 26, 2020 (154)
70 8.3KJPN

Submission ignored due to conflicting rows:
Row 34874938 (NC_000006.11:32627634:T:G 9258/16760)
Row 34874939 (NC_000006.11:32627634:T:C 1/16760)

- Apr 26, 2021 (155)
71 8.3KJPN

Submission ignored due to conflicting rows:
Row 34874938 (NC_000006.11:32627634:T:G 9258/16760)
Row 34874939 (NC_000006.11:32627634:T:C 1/16760)

- Apr 26, 2021 (155)
72 14KJPN

Submission ignored due to conflicting rows:
Row 48612400 (NC_000006.12:32659857:T:G 15776/28258)
Row 48612401 (NC_000006.12:32659857:T:C 1/28258)

- Oct 17, 2022 (156)
73 14KJPN

Submission ignored due to conflicting rows:
Row 48612400 (NC_000006.12:32659857:T:G 15776/28258)
Row 48612401 (NC_000006.12:32659857:T:C 1/28258)

- Oct 17, 2022 (156)
74 TopMed NC_000006.12 - 32659858 Apr 26, 2021 (155)
75 ALFA NC_000006.12 - 32659858 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)
rs35951223 May 23, 2006 (127)
rs76741966 May 04, 2012 (137)
rs79804262 May 04, 2012 (137)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
18253430, ss3911076036 NC_000006.11:32627634:T:A NC_000006.12:32659857:T:A (self)
ss5176905632 NC_000006.11:32627634:T:C NC_000006.12:32659857:T:C (self)
ss5714775297 NC_000006.12:32659857:T:C NC_000006.12:32659857:T:C
ss109918326, ss114162527, ss162212891, ss163366321, ss166456134, ss201646732, ss207767858, ss278739408, ss285379614, ss293830314 NC_000006.10:32735612:T:G NC_000006.12:32659857:T:G (self)
31363080, 12465196, 18253430, 6663400, 8082634, 16315013, 4345849, ss653049963, ss1319594294, ss1926040704, ss1970363127, ss2023654414, ss2151829495, ss2626314914, ss2707423842, ss2998836666, ss3646336462, ss3666726948, ss3733378535, ss3785435412, ss3790793080, ss3795671436, ss3829847515, ss3838401227, ss3864298033, ss3911076036, ss3986035071, ss5176905631, ss5364775554, ss5508436542, ss5640126747, ss5842047778, ss5980359353 NC_000006.11:32627634:T:G NC_000006.12:32659857:T:G (self)
41170053, 221422460, 535956596, 2427736112, ss3025617599, ss3648319559, ss3716935765, ss3807999442, ss3843844657, ss4698579038, ss5267969975, ss5553644118, ss5714775296, ss5807340133, ss5883274344 NC_000006.12:32659857:T:G NC_000006.12:32659857:T:G (self)
ss12698411, ss50397212, ss69378164, ss104299768, ss156765794 NT_007592.15:32567634:T:G NC_000006.12:32659857:T:G (self)
ss4025194438 NT_113891.3:4072798:G:G NC_000006.12:32659857:T:G (self)
ss4025213960 NT_167245.2:3900686:G:G NC_000006.12:32659857:T:G (self)
ss4025234842 NT_167246.2:4077307:G:G NC_000006.12:32659857:T:G (self)
ss4025251399 NT_167247.2:3956224:G:G NC_000006.12:32659857:T:G (self)
ss4025272272 NT_167248.2:3853762:G:G NC_000006.12:32659857:T:G (self)
ss4025293297 NT_167249.2:4057088:G:G NC_000006.12:32659857: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 rs9273444

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