Name: rs1131159
Published: September 21, 2022
License: Open Access

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.

rs1131159

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:31357115 (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 / G>C / G>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.36066 (6740/18688, ALFA)
C=0.47929 (8148/17000, 14KJPN)
G=0.19925 (3339/16758, 8.3KJPN) (+ 7 more)
C=0.27067 (3254/12022, GO-ESP)
G=0.4952 (3171/6404, 1000G_30x)
G=0.2979 (1492/5008, 1000G)
G=0.1769 (517/2922, KOREAN)
G=0.211 (103/488, SGDP_PRJ)
G=0.417 (90/216, Qatari)
G=0.0 (0/8, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HLA-B : Missense Variant
MIR6891 : 2KB Upstream Variant
LOC124905367 : 500B Downstream 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	18688	G=0.63934	A=0.00000, C=0.36066
European	Sub	14118	G=0.62190	A=0.00000, C=0.37810
African	Sub	1682	G=0.8086	A=0.0000, C=0.1914
African Others	Sub	38	G=0.82	A=0.00, C=0.18
African American	Sub	1644	G=0.8084	A=0.0000, C=0.1916
Asian	Sub	100	G=0.65	A=0.00, C=0.35
East Asian	Sub	58	G=0.71	A=0.00, C=0.29
Other Asian	Sub	42	G=0.57	A=0.00, C=0.43
Latin American 1	Sub	66	G=1.00	A=0.00, C=0.00
Latin American 2	Sub	290	G=1.000	A=0.000, C=0.000
South Asian	Sub	14	G=1.00	A=0.00, C=0.00
Other	Sub	2418	G=0.5678	A=0.0000, C=0.4322

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	18688	G=0.63934	A=0.00000, C=0.36066
Allele Frequency Aggregator	European	Sub	14118	G=0.62190	A=0.00000, C=0.37810
Allele Frequency Aggregator	Other	Sub	2418	G=0.5678	A=0.0000, C=0.4322
Allele Frequency Aggregator	African	Sub	1682	G=0.8086	A=0.0000, C=0.1914
Allele Frequency Aggregator	Latin American 2	Sub	290	G=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Asian	Sub	100	G=0.65	A=0.00, C=0.35
Allele Frequency Aggregator	Latin American 1	Sub	66	G=1.00	A=0.00, C=0.00
Allele Frequency Aggregator	South Asian	Sub	14	G=1.00	A=0.00, C=0.00
14KJPN	JAPANESE	Study-wide	17000	G=0.52071	C=0.47929
8.3KJPN	JAPANESE	Study-wide	16758	G=0.19925	C=0.80075
GO Exome Sequencing Project	Global	Study-wide	12022	G=0.72933	C=0.27067
GO Exome Sequencing Project	European American	Sub	7932	G=0.7598	C=0.2402
GO Exome Sequencing Project	African American	Sub	4090	G=0.6702	C=0.3298
1000Genomes_30x	Global	Study-wide	6404	G=0.4952	C=0.5048
1000Genomes_30x	African	Sub	1786	G=0.5011	C=0.4989
1000Genomes_30x	Europe	Sub	1266	G=0.5324	C=0.4676
1000Genomes_30x	South Asian	Sub	1202	G=0.3552	C=0.6448
1000Genomes_30x	East Asian	Sub	1170	G=0.5256	C=0.4744
1000Genomes_30x	American	Sub	980	G=0.571	C=0.429
1000Genomes	Global	Study-wide	5008	G=0.2979	C=0.7021
1000Genomes	African	Sub	1322	G=0.2965	C=0.7035
1000Genomes	East Asian	Sub	1008	G=0.2718	C=0.7282
1000Genomes	Europe	Sub	1006	G=0.3966	C=0.6034
1000Genomes	South Asian	Sub	978	G=0.188	C=0.812
1000Genomes	American	Sub	694	G=0.350	C=0.650
KOREAN population from KRGDB	KOREAN	Study-wide	2922	G=0.1769	C=0.8231
SGDP_PRJ	Global	Study-wide	488	G=0.211	C=0.789
Qatari	Global	Study-wide	216	G=0.417	C=0.583
Siberian	Global	Study-wide	8	G=0.0	C=1.0

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.31357115G>A
GRCh38.p14 chr 6	NC_000006.12:g.31357115G>C
GRCh38.p14 chr 6	NC_000006.12:g.31357115G>T
GRCh37.p13 chr 6	NC_000006.11:g.31324892G>A
GRCh37.p13 chr 6	NC_000006.11:g.31324892G>C
GRCh37.p13 chr 6	NC_000006.11:g.31324892G>T
HLA-B RefSeqGene	NG_023187.1:g.5098C>T
HLA-B RefSeqGene	NG_023187.1:g.5098C>G
HLA-B RefSeqGene	NG_023187.1:g.5098C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2837474G>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2837474G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2837474G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2837580G>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2837580G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2837580G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2699100C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2699100C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2699100C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2704685C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2704685C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2704685C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2612812C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2612812C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2612812C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2618408C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2618408C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2618408C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2659353C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2659353C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2659353C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2658651C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2658651C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2658651C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2665727C>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2665727C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2665727C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2671347C>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2671347C>A
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2671347C>T

Gene: HLA-B, major histocompatibility complex, class I, B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HLA-B transcript	NM_005514.8:c.44C>T	A [GCG] > V [GTG]	Coding Sequence Variant
major histocompatibility complex, class I, B precursor	NP_005505.2:p.Ala15Val	A (Ala) > V (Val)	Missense Variant
HLA-B transcript	NM_005514.8:c.44C>G	A [GCG] > G [GGG]	Coding Sequence Variant
major histocompatibility complex, class I, B precursor	NP_005505.2:p.Ala15Gly	A (Ala) > G (Gly)	Missense Variant
HLA-B transcript	NM_005514.8:c.44C>A	A [GCG] > E [GAG]	Coding Sequence Variant
major histocompatibility complex, class I, B precursor	NP_005505.2:p.Ala15Glu	A (Ala) > E (Glu)	Missense Variant

Gene: MIR6891, microRNA 6891 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
MIR6891 transcript	NR_106951.1:n.	N/A	Upstream Transcript 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.

Not Reported in ClinVar

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	C	T
GRCh38.p14 chr 6	NC_000006.12:g.31357115=	NC_000006.12:g.31357115G>A	NC_000006.12:g.31357115G>C	NC_000006.12:g.31357115G>T
GRCh37.p13 chr 6	NC_000006.11:g.31324892=	NC_000006.11:g.31324892G>A	NC_000006.11:g.31324892G>C	NC_000006.11:g.31324892G>T
HLA-B RefSeqGene	NG_023187.1:g.5098=	NG_023187.1:g.5098C>T	NG_023187.1:g.5098C>G	NG_023187.1:g.5098C>A
HLA-B transcript	NM_005514.8:c.44=	NM_005514.8:c.44C>T	NM_005514.8:c.44C>G	NM_005514.8:c.44C>A
HLA-B transcript	NM_005514.7:c.44=	NM_005514.7:c.44C>T	NM_005514.7:c.44C>G	NM_005514.7:c.44C>A
HLA-B transcript	NM_005514.6:c.44=	NM_005514.6:c.44C>T	NM_005514.6:c.44C>G	NM_005514.6:c.44C>A
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.3:g.2837474=	NT_113891.3:g.2837474G>A	NT_113891.3:g.2837474G>C	NT_113891.3:g.2837474G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1	NT_113891.2:g.2837580=	NT_113891.2:g.2837580G>A	NT_113891.2:g.2837580G>C	NT_113891.2:g.2837580G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.2:g.2699100C>G	NT_167247.2:g.2699100C>A	NT_167247.2:g.2699100=	NT_167247.2:g.2699100C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1	NT_167247.1:g.2704685C>G	NT_167247.1:g.2704685C>A	NT_167247.1:g.2704685=	NT_167247.1:g.2704685C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.2:g.2612812C>G	NT_167248.2:g.2612812C>A	NT_167248.2:g.2612812=	NT_167248.2:g.2612812C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1	NT_167248.1:g.2618408C>G	NT_167248.1:g.2618408C>A	NT_167248.1:g.2618408=	NT_167248.1:g.2618408C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.2:g.2659353C>G	NT_167249.2:g.2659353C>A	NT_167249.2:g.2659353=	NT_167249.2:g.2659353C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1	NT_167249.1:g.2658651C>G	NT_167249.1:g.2658651C>A	NT_167249.1:g.2658651=	NT_167249.1:g.2658651C>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.2:g.2665727C>G	NT_167246.2:g.2665727C>A	NT_167246.2:g.2665727=	NT_167246.2:g.2665727C>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MANN_CTG1	NT_167246.1:g.2671347C>G	NT_167246.1:g.2671347C>A	NT_167246.1:g.2671347=	NT_167246.1:g.2671347C>T
major histocompatibility complex, class I, B precursor	NP_005505.2:p.Ala15=	NP_005505.2:p.Ala15Val	NP_005505.2:p.Ala15Gly	NP_005505.2:p.Ala15Glu

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#.

55 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	LEE	ss4394552	May 29, 2002 (117)
2	SI_MHC_SNP	ss12689713	Oct 31, 2003 (119)
3	1000GENOMES	ss233396586	Jul 14, 2010 (132)
4	1000GENOMES	ss240467643	Jul 15, 2010 (132)
5	PJP	ss293824761	May 09, 2011 (136)
6	EXOME_CHIP	ss491381662	May 04, 2012 (137)
7	CLINSEQ_SNP	ss491884955	May 04, 2012 (137)
8	DBMHC	ss539211642	Oct 03, 2012 (137)
9	SSMP	ss653032169	Apr 25, 2013 (138)
10	NHLBI-ESP	ss712699020	Apr 25, 2013 (138)
11	EVA-GONL	ss982762186	Aug 21, 2014 (142)
12	1000GENOMES	ss1319551063	Aug 21, 2014 (142)
13	EVA_EXAC	ss1688228978	Apr 01, 2015 (144)
14	EVA_EXAC	ss1688228979	Apr 01, 2015 (144)
15	WEILL_CORNELL_DGM	ss1926014106	Feb 12, 2016 (147)
16	JJLAB	ss2023639364	Sep 14, 2016 (149)
17	USC_VALOUEV	ss2151805417	Dec 20, 2016 (150)
18	GRF	ss2707398800	Nov 08, 2017 (151)
19	GNOMAD	ss2735645944	Nov 08, 2017 (151)
20	GNOMAD	ss2747580868	Nov 08, 2017 (151)
21	SWEGEN	ss2998790671	Nov 08, 2017 (151)
22	EVA_SAMSUNG_MC	ss3023062001	Nov 08, 2017 (151)
23	CSIRBIOHTS	ss3029637714	Nov 08, 2017 (151)
24	CSHL	ss3346902006	Nov 08, 2017 (151)
25	OMUKHERJEE_ADBS	ss3646334564	Oct 12, 2018 (152)
26	URBANLAB	ss3648308956	Oct 12, 2018 (152)
27	EVA	ss3764818343	Jul 13, 2019 (153)
28	PACBIO	ss3785424026	Jul 13, 2019 (153)
29	PACBIO	ss3790783455	Jul 13, 2019 (153)
30	PACBIO	ss3795660948	Jul 13, 2019 (153)
31	KHV_HUMAN_GENOMES	ss3807973619	Jul 13, 2019 (153)
32	EVA	ss3824169885	Apr 26, 2020 (154)
33	EVA	ss3825523233	Apr 26, 2020 (154)
34	EVA	ss3825539272	Apr 26, 2020 (154)
35	EVA	ss3829830040	Apr 26, 2020 (154)
36	EVA	ss3843834937	Apr 26, 2020 (154)
37	SGDP_PRJ	ss3864247623	Apr 26, 2020 (154)
38	KRGDB	ss3911022937	Apr 26, 2020 (154)
39	EVA	ss3986034565	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5176827656	Apr 26, 2021 (155)
41	EVA	ss5237022213	Apr 26, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5553584383	Oct 13, 2022 (156)
43	EVA	ss5623935667	Oct 13, 2022 (156)
44	SANFORD_IMAGENETICS	ss5640084026	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5714680228	Oct 13, 2022 (156)
46	EVA	ss5799402789	Oct 13, 2022 (156)
47	EVA	ss5800055567	Oct 13, 2022 (156)
48	EVA	ss5800128918	Oct 13, 2022 (156)
49	YY_MCH	ss5807303268	Oct 13, 2022 (156)
50	EVA	ss5842022060	Oct 13, 2022 (156)
51	EVA	ss5848651110	Oct 13, 2022 (156)
52	EVA	ss5935803119	Oct 13, 2022 (156)
53	EVA	ss5936530626	Oct 13, 2022 (156)
54	EVA	ss5968586318	Oct 13, 2022 (156)
55	EVA	ss5980356030	Oct 13, 2022 (156)
56	1000Genomes	NC_000006.11 - 31324892	Oct 12, 2018 (152)
57	1000Genomes_30x	NC_000006.12 - 31357115	Oct 13, 2022 (156)
58	ExAC Submission ignored due to conflicting rows: Row 8254144 (NC_000006.11:31324891:G:G 39089/65114, NC_000006.11:31324891:G:C 26025/65114) Row 8254145 (NC_000006.11:31324891:G:G 65112/65114, NC_000006.11:31324891:G:A 2/65114)	-	Oct 12, 2018 (152)
59	ExAC Submission ignored due to conflicting rows: Row 8254144 (NC_000006.11:31324891:G:G 39089/65114, NC_000006.11:31324891:G:C 26025/65114) Row 8254145 (NC_000006.11:31324891:G:G 65112/65114, NC_000006.11:31324891:G:A 2/65114)	-	Oct 12, 2018 (152)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221178900 (NC_000006.12:31357114:G:C 3411/46646) Row 221178901 (NC_000006.12:31357114:G:T 1/52748)	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 221178900 (NC_000006.12:31357114:G:C 3411/46646) Row 221178901 (NC_000006.12:31357114:G:T 1/52748)	-	Apr 26, 2021 (155)
62	gnomAD - Exomes Submission ignored due to conflicting rows: Row 4788647 (NC_000006.11:31324891:G:G 79285/138376, NC_000006.11:31324891:G:C 59091/138376) Row 4788648 (NC_000006.11:31324891:G:G 138374/138376, NC_000006.11:31324891:G:T 2/138376)	-	Jul 13, 2019 (153)
63	gnomAD - Exomes Submission ignored due to conflicting rows: Row 4788647 (NC_000006.11:31324891:G:G 79285/138376, NC_000006.11:31324891:G:C 59091/138376) Row 4788648 (NC_000006.11:31324891:G:G 138374/138376, NC_000006.11:31324891:G:T 2/138376)	-	Jul 13, 2019 (153)
64	GO Exome Sequencing Project	NC_000006.11 - 31324892	Oct 12, 2018 (152)
65	KOREAN population from KRGDB	NC_000006.11 - 31324892	Apr 26, 2020 (154)
66	Qatari	NC_000006.11 - 31324892	Apr 26, 2020 (154)
67	SGDP_PRJ	NC_000006.11 - 31324892	Apr 26, 2020 (154)
68	Siberian	NC_000006.11 - 31324892	Apr 26, 2020 (154)
69	8.3KJPN	NC_000006.11 - 31324892	Apr 26, 2021 (155)
70	14KJPN	NC_000006.12 - 31357115	Oct 13, 2022 (156)
71	ALFA	NC_000006.12 - 31357115	Apr 26, 2021 (155)

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)
rs2308336	Aug 27, 2003 (117)
rs3177906	Aug 27, 2003 (117)
rs3190788	Oct 09, 2002 (108)
rs9266202	Dec 04, 2003 (119)
rs116546020	Oct 26, 2010 (133)
rs117887069	Aug 16, 2010 (132)
rs138071825	Mar 28, 2012 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1688228979, ss5935803119	NC_000006.11:31324891:G:A	NC_000006.12:31357114:G:A	(self)
8541740814	NC_000006.12:31357114:G:A	NC_000006.12:31357114:G:A	(self)
ss293824761, ss491884955	NC_000006.10:31432870:G:C	NC_000006.12:31357114:G:C	(self)
31318131, 627928, 18200331, 8056036, 16264603, 4321771, 34796963, ss233396586, ss240467643, ss491381662, ss653032169, ss712699020, ss982762186, ss1319551063, ss1688228978, ss1926014106, ss2023639364, ss2151805417, ss2707398800, ss2735645944, ss2747580868, ss2998790671, ss3023062001, ss3029637714, ss3346902006, ss3646334564, ss3764818343, ss3785424026, ss3790783455, ss3795660948, ss3824169885, ss3825523233, ss3825539272, ss3829830040, ss3864247623, ss3911022937, ss3986034565, ss5176827656, ss5623935667, ss5640084026, ss5799402789, ss5800055567, ss5800128918, ss5842022060, ss5848651110, ss5936530626, ss5968586318, ss5980356030	NC_000006.11:31324891:G:C	NC_000006.12:31357114:G:C	(self)
41110318, 48517332, 8541740814, ss539211642, ss3648308956, ss3807973619, ss3843834937, ss5237022213, ss5553584383, ss5714680228, ss5807303268	NC_000006.12:31357114:G:C	NC_000006.12:31357114:G:C	(self)
ss4394552, ss12689713	NT_007592.15:31264891:G:C	NC_000006.12:31357114:G:C	(self)
ss2735645944	NC_000006.11:31324891:G:T	NC_000006.12:31357114:G:T	(self)
	NC_000006.12:31357114:G:T	NC_000006.12:31357114:G:T	(self)

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

No publications for rs1131159

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1131159