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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.

rs7774255

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr6:29306579 (GRCh38.p13) 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
A=0.417375 (110475/264690, TOPMED)
A=0.441959 (61731/139676, GnomAD)
A=0.48931 (9243/18890, ALFA) (+ 13 more)
A=0.3612 (1809/5008, 1000G)
T=0.4310 (1931/4480, Estonian)
T=0.4966 (1914/3854, ALSPAC)
T=0.4973 (1844/3708, TWINSUK)
A=0.3601 (1055/2930, KOREAN)
T=0.487 (486/998, GoNL)
T=0.458 (275/600, NorthernSweden)
A=0.461 (246/534, MGP)
T=0.325 (111/342, SGDP_PRJ)
A=0.328 (107/326, HapMap)
A=0.407 (88/216, Qatari)
T=0.46 (21/46, Siberian)
T=0.47 (19/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
OR14J1 : Intron Variant
LOC105375005 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
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.p13 chr 6 NC_000006.12:g.29306579T>A
GRCh38.p13 chr 6 NC_000006.12:g.29306579T>C
GRCh38.p13 chr 6 NC_000006.12:g.29306579T>G
GRCh37.p13 chr 6 NC_000006.11:g.29274356T>A
GRCh37.p13 chr 6 NC_000006.11:g.29274356T>C
GRCh37.p13 chr 6 NC_000006.11:g.29274356T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.793169T>A
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.793169T>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.793169T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.793275T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.793275T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.793275T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.572222A>T
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.572222A>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.572222A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.577807A>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.577807A>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.577807A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.616012A>T
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.616012A>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.616012A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.615310A>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.615310A>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.615310A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.572181A>T
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.572181A>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.572181A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.577801A>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.577801A>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.577801A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.572402T>A
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.572402T>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.572402T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.577987T>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.577987T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.577987T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.572245A>T
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.572245A>C
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.572245A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.577839A>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.577839A>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.577839A>G
Gene: OR14J1, olfactory receptor family 14 subfamily J member 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
OR14J1 transcript NM_030946.2:c.-28-83T>A N/A Intron Variant
Gene: LOC105375005, uncharacterized LOC105375005 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105375005 transcript variant X3 XR_926670.1:n. N/A Intron Variant
LOC105375005 transcript variant X1 XR_001744074.1:n. N/A Genic Downstream Transcript Variant
LOC105375005 transcript variant X2 XR_001744075.1:n. N/A Genic Downstream 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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 18890 T=0.51069 A=0.48931
European Sub 14286 T=0.46080 A=0.53920
African Sub 2946 T=0.7135 A=0.2865
African Others Sub 114 T=0.798 A=0.202
African American Sub 2832 T=0.7101 A=0.2899
Asian Sub 112 T=0.571 A=0.429
East Asian Sub 86 T=0.58 A=0.42
Other Asian Sub 26 T=0.54 A=0.46
Latin American 1 Sub 146 T=0.623 A=0.377
Latin American 2 Sub 610 T=0.592 A=0.408
South Asian Sub 98 T=0.60 A=0.40
Other Sub 692 T=0.559 A=0.441


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=0.582625 A=0.417375
gnomAD - Genomes Global Study-wide 139676 T=0.558041 A=0.441959
gnomAD - Genomes European Sub 75582 T=0.46163 A=0.53837
gnomAD - Genomes African Sub 41916 T=0.71085 A=0.28915
gnomAD - Genomes American Sub 13606 T=0.58437 A=0.41563
gnomAD - Genomes Ashkenazi Jewish Sub 3316 T=0.5805 A=0.4195
gnomAD - Genomes East Asian Sub 3114 T=0.6795 A=0.3205
gnomAD - Genomes Other Sub 2142 T=0.5910 A=0.4090
1000Genomes Global Study-wide 5008 T=0.6388 A=0.3612
1000Genomes African Sub 1322 T=0.7920 A=0.2080
1000Genomes East Asian Sub 1008 T=0.6677 A=0.3323
1000Genomes Europe Sub 1006 T=0.4682 A=0.5318
1000Genomes South Asian Sub 978 T=0.615 A=0.385
1000Genomes American Sub 694 T=0.586 A=0.414
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.4310 A=0.5690
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.4966 A=0.5034
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.4973 A=0.5027
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.6399 A=0.3601, C=0.0000
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.487 A=0.513
Northern Sweden ACPOP Study-wide 600 T=0.458 A=0.542
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.539 A=0.461
SGDP_PRJ Global Study-wide 342 T=0.325 A=0.675
HapMap Global Study-wide 326 T=0.672 A=0.328
HapMap African Sub 120 T=0.833 A=0.167
HapMap American Sub 120 T=0.467 A=0.533
HapMap Asian Sub 86 T=0.73 A=0.27
Qatari Global Study-wide 216 T=0.593 A=0.407
Siberian Global Study-wide 46 T=0.46 A=0.54
The Danish reference pan genome Danish Study-wide 40 T=0.47 A=0.53
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.p13 chr 6 NC_000006.12:g.29306579= NC_000006.12:g.29306579T>A NC_000006.12:g.29306579T>C NC_000006.12:g.29306579T>G
GRCh37.p13 chr 6 NC_000006.11:g.29274356= NC_000006.11:g.29274356T>A NC_000006.11:g.29274356T>C NC_000006.11:g.29274356T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.793169= NT_113891.3:g.793169T>A NT_113891.3:g.793169T>C NT_113891.3:g.793169T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.793275= NT_113891.2:g.793275T>A NT_113891.2:g.793275T>C NT_113891.2:g.793275T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.572222A>T NT_167245.2:g.572222= NT_167245.2:g.572222A>C NT_167245.2:g.572222A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.577807A>T NT_167245.1:g.577807= NT_167245.1:g.577807A>C NT_167245.1:g.577807A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.616012A>T NT_167249.2:g.616012= NT_167249.2:g.616012A>C NT_167249.2:g.616012A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.615310A>T NT_167249.1:g.615310= NT_167249.1:g.615310A>C NT_167249.1:g.615310A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.2:g.572181A>T NT_167246.2:g.572181= NT_167246.2:g.572181A>C NT_167246.2:g.572181A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1 NT_167246.1:g.577801A>T NT_167246.1:g.577801= NT_167246.1:g.577801A>C NT_167246.1:g.577801A>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.572402= NT_167247.2:g.572402T>A NT_167247.2:g.572402T>C NT_167247.2:g.572402T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.577987= NT_167247.1:g.577987T>A NT_167247.1:g.577987T>C NT_167247.1:g.577987T>G
GRCh38.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.572245A>T NT_167244.2:g.572245= NT_167244.2:g.572245A>C NT_167244.2:g.572245A>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.577839A>T NT_167244.1:g.577839= NT_167244.1:g.577839A>C NT_167244.1:g.577839A>G
OR14J1 transcript NM_030946.2:c.-28-83= NM_030946.2:c.-28-83T>A NM_030946.2:c.-28-83T>C NM_030946.2:c.-28-83T>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#.

105 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss11838340 Jul 11, 2003 (116)
2 SI_MHC_SNP ss12677140 Oct 31, 2003 (118)
3 SC_SNP ss14794892 Dec 05, 2003 (119)
4 CSHL-HAPMAP ss19672108 Feb 27, 2004 (120)
5 SSAHASNP ss22508289 Apr 05, 2004 (121)
6 ABI ss44727704 Mar 14, 2006 (126)
7 KRIBB_YJKIM ss65847450 Nov 30, 2006 (127)
8 CSHL-HAPMAP ss68421491 Jan 12, 2007 (127)
9 ILLUMINA ss75264705 Dec 07, 2007 (129)
10 SI_EXO ss76896867 Dec 07, 2007 (129)
11 BCMHGSC_JDW ss93430174 Mar 24, 2008 (129)
12 HUMANGENOME_JCVI ss98484501 Feb 05, 2009 (130)
13 BGI ss104290599 Dec 01, 2009 (131)
14 1000GENOMES ss109864875 Feb 13, 2009 (137)
15 1000GENOMES ss114085857 Jan 25, 2009 (137)
16 KRIBB_YJKIM ss119568342 Dec 01, 2009 (131)
17 ENSEMBL ss134588650 Dec 01, 2009 (131)
18 GMI ss156686875 Dec 01, 2009 (131)
19 ILLUMINA ss160913481 Dec 01, 2009 (131)
20 COMPLETE_GENOMICS ss162157065 Jul 04, 2010 (132)
21 COMPLETE_GENOMICS ss163296977 Jul 04, 2010 (132)
22 COMPLETE_GENOMICS ss166353466 Jul 04, 2010 (132)
23 ILLUMINA ss174541449 Jul 04, 2010 (135)
24 BUSHMAN ss201578428 Jul 04, 2010 (132)
25 1000GENOMES ss222282413 Jul 14, 2010 (137)
26 1000GENOMES ss233379085 Jul 14, 2010 (137)
27 1000GENOMES ss240450909 Jul 15, 2010 (137)
28 GMI ss278705785 May 04, 2012 (137)
29 GMI ss285365367 Apr 25, 2013 (138)
30 ILLUMINA ss481671128 May 04, 2012 (137)
31 ILLUMINA ss481701882 May 04, 2012 (137)
32 ILLUMINA ss482669305 Sep 08, 2015 (146)
33 ILLUMINA ss485630198 May 04, 2012 (137)
34 ILLUMINA ss532828720 Sep 08, 2015 (146)
35 ILLUMINA ss537512519 Sep 08, 2015 (146)
36 TISHKOFF ss559093522 Apr 25, 2013 (138)
37 SSMP ss653007819 Apr 25, 2013 (138)
38 ILLUMINA ss778342319 Sep 08, 2015 (146)
39 ILLUMINA ss783260697 Sep 08, 2015 (146)
40 ILLUMINA ss784214142 Sep 08, 2015 (146)
41 ILLUMINA ss832521612 Sep 08, 2015 (146)
42 ILLUMINA ss833796929 Sep 08, 2015 (146)
43 EVA-GONL ss982730314 Aug 21, 2014 (142)
44 JMKIDD_LAB ss1073483938 Aug 21, 2014 (142)
45 1000GENOMES ss1319483938 Aug 21, 2014 (142)
46 EVA_GENOME_DK ss1581589803 Apr 01, 2015 (144)
47 EVA_DECODE ss1592280670 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1615233881 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1658227914 Apr 01, 2015 (144)
50 EVA_MGP ss1711116641 Apr 01, 2015 (144)
51 EVA_SVP ss1712847156 Apr 01, 2015 (144)
52 ILLUMINA ss1752623577 Sep 08, 2015 (146)
53 HAMMER_LAB ss1804339792 Sep 08, 2015 (146)
54 WEILL_CORNELL_DGM ss1925982346 Feb 12, 2016 (147)
55 GENOMED ss1970345304 Jul 19, 2016 (147)
56 JJLAB ss2023615765 Sep 14, 2016 (149)
57 ILLUMINA ss2094821239 Dec 20, 2016 (150)
58 ILLUMINA ss2095172536 Dec 20, 2016 (150)
59 USC_VALOUEV ss2151780150 Nov 08, 2017 (151)
60 HUMAN_LONGEVITY ss2282829392 Dec 20, 2016 (150)
61 TOPMED ss2451198036 Dec 20, 2016 (150)
62 SYSTEMSBIOZJU ss2626293807 Nov 08, 2017 (151)
63 ILLUMINA ss2634421027 Nov 08, 2017 (151)
64 GRF ss2707372159 Nov 08, 2017 (151)
65 AFFY ss2985989142 Nov 08, 2017 (151)
66 SWEGEN ss2998741118 Nov 08, 2017 (151)
67 BIOINF_KMB_FNS_UNIBA ss3025592873 Nov 08, 2017 (151)
68 TOPMED ss3493451013 Nov 08, 2017 (151)
69 ILLUMINA ss3629484911 Oct 12, 2018 (152)
70 ILLUMINA ss3629484912 Oct 12, 2018 (152)
71 ILLUMINA ss3632340512 Oct 12, 2018 (152)
72 ILLUMINA ss3633412316 Oct 12, 2018 (152)
73 ILLUMINA ss3634134566 Oct 12, 2018 (152)
74 ILLUMINA ss3635052007 Oct 12, 2018 (152)
75 ILLUMINA ss3635815748 Oct 12, 2018 (152)
76 ILLUMINA ss3636770297 Oct 12, 2018 (152)
77 ILLUMINA ss3637568487 Oct 12, 2018 (152)
78 ILLUMINA ss3638615682 Oct 12, 2018 (152)
79 ILLUMINA ss3640759303 Oct 12, 2018 (152)
80 ILLUMINA ss3643556921 Oct 12, 2018 (152)
81 URBANLAB ss3648299978 Oct 12, 2018 (152)
82 ILLUMINA ss3653098219 Oct 12, 2018 (152)
83 EGCUT_WGS ss3666669320 Jul 13, 2019 (153)
84 EVA_DECODE ss3716854871 Jul 13, 2019 (153)
85 ACPOP ss3733325490 Jul 13, 2019 (153)
86 ILLUMINA ss3745352079 Jul 13, 2019 (153)
87 EVA ss3764783737 Jul 13, 2019 (153)
88 ILLUMINA ss3772845819 Jul 13, 2019 (153)
89 PACBIO ss3785411737 Jul 13, 2019 (153)
90 PACBIO ss3790771804 Jul 13, 2019 (153)
91 PACBIO ss3795649162 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3807939789 Jul 13, 2019 (153)
93 EVA ss3829807214 Apr 26, 2020 (154)
94 EVA ss3838380894 Apr 26, 2020 (154)
95 EVA ss3843821876 Apr 26, 2020 (154)
96 SGDP_PRJ ss3864193015 Apr 26, 2020 (154)
97 KRGDB ss3910967387 Apr 26, 2020 (154)
98 EVA ss4017263036 Apr 26, 2021 (155)
99 VINODS ss4025166879 Apr 26, 2021 (155)
100 VINODS ss4025199125 Apr 26, 2021 (155)
101 VINODS ss4025218362 Apr 26, 2021 (155)
102 VINODS ss4025277510 Apr 26, 2021 (155)
103 TOPMED ss4697933066 Apr 26, 2021 (155)
104 TOMMO_GENOMICS ss5176742326 Apr 26, 2021 (155)
105 TOMMO_GENOMICS ss5176742327 Apr 26, 2021 (155)
106 1000Genomes NC_000006.11 - 29274356 Oct 12, 2018 (152)
107 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 29274356 Oct 12, 2018 (152)
108 Genetic variation in the Estonian population NC_000006.11 - 29274356 Oct 12, 2018 (152)
109 The Danish reference pan genome NC_000006.11 - 29274356 Apr 26, 2020 (154)
110 gnomAD - Genomes NC_000006.12 - 29306579 Apr 26, 2021 (155)
111 Genome of the Netherlands Release 5 NC_000006.11 - 29274356 Apr 26, 2020 (154)
112 HapMap NC_000006.12 - 29306579 Apr 26, 2020 (154)
113 KOREAN population from KRGDB NC_000006.11 - 29274356 Apr 26, 2020 (154)
114 Medical Genome Project healthy controls from Spanish population NC_000006.11 - 29274356 Apr 26, 2020 (154)
115 Northern Sweden NC_000006.11 - 29274356 Jul 13, 2019 (153)
116 Qatari NC_000006.11 - 29274356 Apr 26, 2020 (154)
117 SGDP_PRJ NC_000006.11 - 29274356 Apr 26, 2020 (154)
118 Siberian NC_000006.11 - 29274356 Apr 26, 2020 (154)
119 8.3KJPN

Submission ignored due to conflicting rows:
Row 34711633 (NC_000006.11:29274355:T:A 5537/16760)
Row 34711634 (NC_000006.11:29274355:T:G 1/16760)

- Apr 26, 2021 (155)
120 8.3KJPN

Submission ignored due to conflicting rows:
Row 34711633 (NC_000006.11:29274355:T:A 5537/16760)
Row 34711634 (NC_000006.11:29274355:T:G 1/16760)

- Apr 26, 2021 (155)
121 TopMed NC_000006.12 - 29306579 Apr 26, 2021 (155)
122 UK 10K study - Twins NC_000006.11 - 29274356 Oct 12, 2018 (152)
123 ALFA NC_000006.12 - 29306579 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)
rs111831678 Sep 17, 2011 (135)
rs114962395 May 04, 2012 (137)
rs117687304 Aug 16, 2010 (132)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss93430174, ss109864875, ss114085857, ss162157065, ss163296977, ss166353466, ss201578428, ss278705785, ss285365367, ss481671128, ss1592280670, ss1712847156, ss3643556921 NC_000006.10:29382334:T:A NC_000006.12:29306578:T:A (self)
31248234, 17418521, 12407568, 7754742, 7730996, 18144781, 232401, 6610355, 8024276, 16209995, 4296504, 17418521, ss222282413, ss233379085, ss240450909, ss481701882, ss482669305, ss485630198, ss532828720, ss537512519, ss559093522, ss653007819, ss778342319, ss783260697, ss784214142, ss832521612, ss833796929, ss982730314, ss1073483938, ss1319483938, ss1581589803, ss1615233881, ss1658227914, ss1711116641, ss1752623577, ss1804339792, ss1925982346, ss1970345304, ss2023615765, ss2094821239, ss2095172536, ss2151780150, ss2451198036, ss2626293807, ss2634421027, ss2707372159, ss2985989142, ss2998741118, ss3629484911, ss3629484912, ss3632340512, ss3633412316, ss3634134566, ss3635052007, ss3635815748, ss3636770297, ss3637568487, ss3638615682, ss3640759303, ss3653098219, ss3666669320, ss3733325490, ss3745352079, ss3764783737, ss3772845819, ss3785411737, ss3790771804, ss3795649162, ss3829807214, ss3838380894, ss3864193015, ss3910967387, ss4017263036, ss5176742326 NC_000006.11:29274355:T:A NC_000006.12:29306578:T:A (self)
220787974, 3092200, 334757796, 535310624, 4283904558, ss2282829392, ss3025592873, ss3493451013, ss3648299978, ss3716854871, ss3807939789, ss3843821876, ss4697933066 NC_000006.12:29306578:T:A NC_000006.12:29306578:T:A (self)
ss11838340, ss14794892, ss19672108, ss22508289 NT_007592.13:20132637:T:A NC_000006.12:29306578:T:A (self)
ss76896867 NT_007592.14:20132606:T:A NC_000006.12:29306578:T:A (self)
ss12677140, ss44727704, ss65847450, ss68421491, ss75264705, ss98484501, ss104290599, ss119568342, ss134588650, ss156686875, ss160913481, ss174541449 NT_007592.15:29214355:T:A NC_000006.12:29306578:T:A (self)
ss4025166879 NT_167244.2:572244:A:A NC_000006.12:29306578:T:A
ss4025199125 NT_167245.2:572221:A:A NC_000006.12:29306578:T:A
ss4025218362 NT_167246.2:572180:A:A NC_000006.12:29306578:T:A
ss4025277510 NT_167249.2:616011:A:A NC_000006.12:29306578:T:A
18144781, ss3910967387 NC_000006.11:29274355:T:C NC_000006.12:29306578:T:C (self)
ss5176742327 NC_000006.11:29274355:T:G NC_000006.12:29306578:T:G
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 rs7774255

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.post596+ae089ad