Name: rs11575231
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.

rs11575231

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:56350661 (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
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.04374 (1236/28258, 14KJPN)
C=0.02446 (429/17540, ALFA)
C=0.04433 (743/16760, 8.3KJPN) (+ 13 more)
C=0.0312 (200/6404, 1000G_30x)
C=0.0315 (158/5008, 1000G)
C=0.0931 (417/4480, Estonian)
C=0.0462 (135/2922, KOREAN)
C=0.0404 (74/1832, Korea1K)
C=0.063 (63/998, GoNL)
C=0.055 (33/600, NorthernSweden)
C=0.005 (1/216, Qatari)
C=0.019 (4/216, Vietnamese)
T=0.44 (30/68, SGDP_PRJ)
C=0.03 (1/40, GENOME_DK)
T=0.5 (5/10, Siberian)
C=0.5 (5/10, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STAT2 : 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	17540	T=0.97554	A=0.00000, C=0.02446
European	Sub	13080	T=0.96789	A=0.00000, C=0.03211
African	Sub	2896	T=1.0000	A=0.0000, C=0.0000
African Others	Sub	114	T=1.000	A=0.000, C=0.000
African American	Sub	2782	T=1.0000	A=0.0000, C=0.0000
Asian	Sub	106	T=1.000	A=0.000, C=0.000
East Asian	Sub	84	T=1.00	A=0.00, C=0.00
Other Asian	Sub	22	T=1.00	A=0.00, C=0.00
Latin American 1	Sub	138	T=1.000	A=0.000, C=0.000
Latin American 2	Sub	548	T=1.000	A=0.000, C=0.000
South Asian	Sub	98	T=1.00	A=0.00, C=0.00
Other	Sub	674	T=0.987	A=0.000, C=0.013

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
14KJPN	JAPANESE	Study-wide	28258	T=0.95626	C=0.04374
Allele Frequency Aggregator	Total	Global	17540	T=0.97554	A=0.00000, C=0.02446
Allele Frequency Aggregator	European	Sub	13080	T=0.96789	A=0.00000, C=0.03211
Allele Frequency Aggregator	African	Sub	2896	T=1.0000	A=0.0000, C=0.0000
Allele Frequency Aggregator	Other	Sub	674	T=0.987	A=0.000, C=0.013
Allele Frequency Aggregator	Latin American 2	Sub	548	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	Asian	Sub	106	T=1.000	A=0.000, C=0.000
Allele Frequency Aggregator	South Asian	Sub	98	T=1.00	A=0.00, C=0.00
8.3KJPN	JAPANESE	Study-wide	16760	T=0.95567	C=0.04433
1000Genomes_30x	Global	Study-wide	6404	T=0.9688	C=0.0312
1000Genomes_30x	African	Sub	1786	T=0.9989	C=0.0011
1000Genomes_30x	Europe	Sub	1266	T=0.9352	C=0.0648
1000Genomes_30x	South Asian	Sub	1202	T=0.9800	C=0.0200
1000Genomes_30x	East Asian	Sub	1170	T=0.9667	C=0.0333
1000Genomes_30x	American	Sub	980	T=0.946	C=0.054
1000Genomes	Global	Study-wide	5008	T=0.9685	C=0.0315
1000Genomes	African	Sub	1322	T=0.9985	C=0.0015
1000Genomes	East Asian	Sub	1008	T=0.9643	C=0.0357
1000Genomes	Europe	Sub	1006	T=0.9354	C=0.0646
1000Genomes	South Asian	Sub	978	T=0.981	C=0.019
1000Genomes	American	Sub	694	T=0.948	C=0.052
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.9069	C=0.0931
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.9538	C=0.0462
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9596	C=0.0404
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.937	C=0.063
Northern Sweden	ACPOP	Study-wide	600	T=0.945	C=0.055
Qatari	Global	Study-wide	216	T=0.995	C=0.005
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.981	C=0.019
SGDP_PRJ	Global	Study-wide	68	T=0.44	C=0.56
The Danish reference pan genome	Danish	Study-wide	40	T=0.97	C=0.03
Siberian	Global	Study-wide	10	T=0.5	C=0.5

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 12	NC_000012.12:g.56350661T>A
GRCh38.p14 chr 12	NC_000012.12:g.56350661T>C
GRCh37.p13 chr 12	NC_000012.11:g.56744445T>A
GRCh37.p13 chr 12	NC_000012.11:g.56744445T>C
STAT2 RefSeqGene (LRG_1329)	NG_046314.1:g.14593A>T
STAT2 RefSeqGene (LRG_1329)	NG_046314.1:g.14593A>G

Gene: STAT2, signal transducer and activator of transcription 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
STAT2 transcript variant 3	NM_001385110.1:c.1082+168… NM_001385110.1:c.1082+168A>T	N/A	Intron Variant
STAT2 transcript variant 4	NM_001385111.1:c.1094+168… NM_001385111.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant 5	NM_001385113.1:c.1094+168… NM_001385113.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant 6	NM_001385114.1:c.1094+168… NM_001385114.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant 7	NM_001385115.1:c.1082+168… NM_001385115.1:c.1082+168A>T	N/A	Intron Variant
STAT2 transcript variant 1	NM_005419.4:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant 2	NM_198332.2:c.1082+168A>T	N/A	Intron Variant
STAT2 transcript variant X1	XM_011538697.3:c.1094+168… XM_011538697.3:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X2	XM_011538698.4:c.1082+168… XM_011538698.4:c.1082+168A>T	N/A	Intron Variant
STAT2 transcript variant X3	XM_011538699.4:c.1094+168… XM_011538699.4:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X4	XM_047429468.1:c.1094+168… XM_047429468.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X5	XM_047429469.1:c.125+168A… XM_047429469.1:c.125+168A>T	N/A	Intron Variant
STAT2 transcript variant X6	XM_047429470.1:c.1094+168… XM_047429470.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X8	XM_047429471.1:c.1094+168… XM_047429471.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X9	XM_047429472.1:c.1094+168… XM_047429472.1:c.1094+168A>T	N/A	Intron Variant
STAT2 transcript variant X10	XR_007063122.1:n.	N/A	Intron Variant
STAT2 transcript variant X7	XR_245953.4:n.	N/A	Intron 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	T=	A	C
GRCh38.p14 chr 12	NC_000012.12:g.56350661=	NC_000012.12:g.56350661T>A	NC_000012.12:g.56350661T>C
GRCh37.p13 chr 12	NC_000012.11:g.56744445=	NC_000012.11:g.56744445T>A	NC_000012.11:g.56744445T>C
STAT2 RefSeqGene (LRG_1329)	NG_046314.1:g.14593=	NG_046314.1:g.14593A>T	NG_046314.1:g.14593A>G
STAT2 transcript variant 3	NM_001385110.1:c.1082+168=	NM_001385110.1:c.1082+168A>T	NM_001385110.1:c.1082+168A>G
STAT2 transcript variant 4	NM_001385111.1:c.1094+168=	NM_001385111.1:c.1094+168A>T	NM_001385111.1:c.1094+168A>G
STAT2 transcript variant 5	NM_001385113.1:c.1094+168=	NM_001385113.1:c.1094+168A>T	NM_001385113.1:c.1094+168A>G
STAT2 transcript variant 6	NM_001385114.1:c.1094+168=	NM_001385114.1:c.1094+168A>T	NM_001385114.1:c.1094+168A>G
STAT2 transcript variant 7	NM_001385115.1:c.1082+168=	NM_001385115.1:c.1082+168A>T	NM_001385115.1:c.1082+168A>G
STAT2 transcript variant 1	NM_005419.3:c.1094+168=	NM_005419.3:c.1094+168A>T	NM_005419.3:c.1094+168A>G
STAT2 transcript variant 1	NM_005419.4:c.1094+168=	NM_005419.4:c.1094+168A>T	NM_005419.4:c.1094+168A>G
STAT2 transcript variant 2	NM_198332.1:c.1082+168=	NM_198332.1:c.1082+168A>T	NM_198332.1:c.1082+168A>G
STAT2 transcript variant 2	NM_198332.2:c.1082+168=	NM_198332.2:c.1082+168A>T	NM_198332.2:c.1082+168A>G
STAT2 transcript variant X1	XM_005269108.1:c.1298+168=	XM_005269108.1:c.1298+168A>T	XM_005269108.1:c.1298+168A>G
STAT2 transcript variant X2	XM_005269109.1:c.1286+168=	XM_005269109.1:c.1286+168A>T	XM_005269109.1:c.1286+168A>G
STAT2 transcript variant X3	XM_005269110.1:c.1298+168=	XM_005269110.1:c.1298+168A>T	XM_005269110.1:c.1298+168A>G
STAT2 transcript variant X4	XM_005269111.1:c.1298+168=	XM_005269111.1:c.1298+168A>T	XM_005269111.1:c.1298+168A>G
STAT2 transcript variant X1	XM_011538697.3:c.1094+168=	XM_011538697.3:c.1094+168A>T	XM_011538697.3:c.1094+168A>G
STAT2 transcript variant X2	XM_011538698.4:c.1082+168=	XM_011538698.4:c.1082+168A>T	XM_011538698.4:c.1082+168A>G
STAT2 transcript variant X3	XM_011538699.4:c.1094+168=	XM_011538699.4:c.1094+168A>T	XM_011538699.4:c.1094+168A>G
STAT2 transcript variant X4	XM_047429468.1:c.1094+168=	XM_047429468.1:c.1094+168A>T	XM_047429468.1:c.1094+168A>G
STAT2 transcript variant X5	XM_047429469.1:c.125+168=	XM_047429469.1:c.125+168A>T	XM_047429469.1:c.125+168A>G
STAT2 transcript variant X6	XM_047429470.1:c.1094+168=	XM_047429470.1:c.1094+168A>T	XM_047429470.1:c.1094+168A>G
STAT2 transcript variant X8	XM_047429471.1:c.1094+168=	XM_047429471.1:c.1094+168A>T	XM_047429471.1:c.1094+168A>G
STAT2 transcript variant X9	XM_047429472.1:c.1094+168=	XM_047429472.1:c.1094+168A>T	XM_047429472.1:c.1094+168A>G

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#.

54 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EGP_SNPS	ss16361216	Feb 28, 2004 (120)
2	CGM_KYOTO	ss76872924	Dec 06, 2007 (129)
3	1000GENOMES	ss235946382	Jul 15, 2010 (132)
4	1000GENOMES	ss242503774	Jul 15, 2010 (132)
5	GMI	ss281409001	May 04, 2012 (137)
6	SSMP	ss658743964	Apr 25, 2013 (138)
7	EVA-GONL	ss989565865	Aug 21, 2014 (142)
8	JMKIDD_LAB	ss1078483883	Aug 21, 2014 (142)
9	1000GENOMES	ss1345148021	Aug 21, 2014 (142)
10	EVA_GENOME_DK	ss1576302322	Apr 01, 2015 (144)
11	EVA_DECODE	ss1599239359	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1628656824	Apr 01, 2015 (144)
13	EVA_UK10K_ALSPAC	ss1628656825	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1671650857	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1671650858	Apr 01, 2015 (144)
16	WEILL_CORNELL_DGM	ss1932931714	Feb 12, 2016 (147)
17	JJLAB	ss2027215836	Sep 14, 2016 (149)
18	ILLUMINA	ss2094874530	Dec 20, 2016 (150)
19	ILLUMINA	ss2095035609	Dec 20, 2016 (150)
20	USC_VALOUEV	ss2155556588	Dec 20, 2016 (150)
21	HUMAN_LONGEVITY	ss2190055824	Dec 20, 2016 (150)
22	SYSTEMSBIOZJU	ss2628089243	Nov 08, 2017 (151)
23	GRF	ss2699901332	Nov 08, 2017 (151)
24	GNOMAD	ss2910887840	Nov 08, 2017 (151)
25	AFFY	ss2984980375	Nov 08, 2017 (151)
26	SWEGEN	ss3009744509	Nov 08, 2017 (151)
27	BIOINF_KMB_FNS_UNIBA	ss3027416760	Nov 08, 2017 (151)
28	CSHL	ss3350079353	Nov 08, 2017 (151)
29	ILLUMINA	ss3651812972	Oct 12, 2018 (152)
30	EGCUT_WGS	ss3677013421	Jul 13, 2019 (153)
31	EVA_DECODE	ss3693735542	Jul 13, 2019 (153)
32	ACPOP	ss3739050700	Jul 13, 2019 (153)
33	EVA	ss3750519142	Jul 13, 2019 (153)
34	KHV_HUMAN_GENOMES	ss3815849775	Jul 13, 2019 (153)
35	SGDP_PRJ	ss3878343013	Apr 27, 2020 (154)
36	KRGDB	ss3926987453	Apr 27, 2020 (154)
37	KOGIC	ss3972007926	Apr 27, 2020 (154)
38	FSA-LAB	ss3984030572	Apr 26, 2021 (155)
39	EVA	ss3986573950	Apr 26, 2021 (155)
40	TOPMED	ss4919456239	Apr 26, 2021 (155)
41	TOPMED	ss4919456240	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5206478604	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5290927765	Oct 16, 2022 (156)
44	EVA	ss5405844998	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5485665388	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5588470043	Oct 16, 2022 (156)
47	SANFORD_IMAGENETICS	ss5653220223	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5756318427	Oct 16, 2022 (156)
49	YY_MCH	ss5813327007	Oct 16, 2022 (156)
50	EVA	ss5838010526	Oct 16, 2022 (156)
51	EVA	ss5848354855	Oct 16, 2022 (156)
52	EVA	ss5850395587	Oct 16, 2022 (156)
53	EVA	ss5904524057	Oct 16, 2022 (156)
54	EVA	ss5944582688	Oct 16, 2022 (156)
55	1000Genomes	NC_000012.11 - 56744445	Oct 12, 2018 (152)
56	1000Genomes_30x	NC_000012.12 - 56350661	Oct 16, 2022 (156)
57	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32147977 (NC_000012.11:56744444:T:T 3611/3854, NC_000012.11:56744444:T:C 243/3854) Row 32147978 (NC_000012.11:56744444:T:T 3853/3854, NC_000012.11:56744444:T:A 1/3854)	-	Oct 12, 2018 (152)
58	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 32147977 (NC_000012.11:56744444:T:T 3611/3854, NC_000012.11:56744444:T:C 243/3854) Row 32147978 (NC_000012.11:56744444:T:T 3853/3854, NC_000012.11:56744444:T:A 1/3854)	-	Oct 12, 2018 (152)
59	Genetic variation in the Estonian population	NC_000012.11 - 56744445	Oct 12, 2018 (152)
60	The Danish reference pan genome	NC_000012.11 - 56744445	Apr 27, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408318749 (NC_000012.12:56350660:T:A 2/140216) Row 408318750 (NC_000012.12:56350660:T:C 6455/140212)	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 408318749 (NC_000012.12:56350660:T:A 2/140216) Row 408318750 (NC_000012.12:56350660:T:C 6455/140212)	-	Apr 26, 2021 (155)
63	Genome of the Netherlands Release 5	NC_000012.11 - 56744445	Apr 27, 2020 (154)
64	KOREAN population from KRGDB	NC_000012.11 - 56744445	Apr 27, 2020 (154)
65	Korean Genome Project	NC_000012.12 - 56350661	Apr 27, 2020 (154)
66	Northern Sweden	NC_000012.11 - 56744445	Jul 13, 2019 (153)
67	Qatari	NC_000012.11 - 56744445	Apr 27, 2020 (154)
68	SGDP_PRJ	NC_000012.11 - 56744445	Apr 27, 2020 (154)
69	Siberian	NC_000012.11 - 56744445	Apr 27, 2020 (154)
70	8.3KJPN	NC_000012.11 - 56744445	Apr 26, 2021 (155)
71	14KJPN	NC_000012.12 - 56350661	Oct 16, 2022 (156)
72	TopMed Submission ignored due to conflicting rows: Row 135001896 (NC_000012.12:56350660:T:A 3/264690) Row 135001897 (NC_000012.12:56350660:T:C 11160/264690)	-	Apr 26, 2021 (155)
73	TopMed Submission ignored due to conflicting rows: Row 135001896 (NC_000012.12:56350660:T:A 3/264690) Row 135001897 (NC_000012.12:56350660:T:C 11160/264690)	-	Apr 26, 2021 (155)
74	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32147977 (NC_000012.11:56744444:T:T 3460/3708, NC_000012.11:56744444:T:C 248/3708) Row 32147978 (NC_000012.11:56744444:T:T 3708/3708, NC_000012.11:56744444:T:A 0/3708)	-	Oct 12, 2018 (152)
75	UK 10K study - Twins Submission ignored due to conflicting rows: Row 32147977 (NC_000012.11:56744444:T:T 3460/3708, NC_000012.11:56744444:T:C 248/3708) Row 32147978 (NC_000012.11:56744444:T:T 3708/3708, NC_000012.11:56744444:T:A 0/3708)	-	Oct 12, 2018 (152)
76	A Vietnamese Genetic Variation Database	NC_000012.11 - 56744445	Jul 13, 2019 (153)
77	ALFA	NC_000012.12 - 56350661	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1628656825, ss1671650858	NC_000012.11:56744444:T:A	NC_000012.12:56350660:T:A	(self)
9359334750, ss4919456239	NC_000012.12:56350660:T:A	NC_000012.12:56350660:T:A	(self)
ss281409001, ss1599239359, ss2094874530	NC_000012.10:55030711:T:C	NC_000012.12:56350660:T:C	(self)
57901536, 22751669, 2975882, 14344362, 34164847, 12335565, 14973644, 30359993, 8072942, 64447911, 7136247, ss235946382, ss242503774, ss658743964, ss989565865, ss1078483883, ss1345148021, ss1576302322, ss1628656824, ss1671650857, ss1932931714, ss2027215836, ss2095035609, ss2155556588, ss2628089243, ss2699901332, ss2910887840, ss2984980375, ss3009744509, ss3350079353, ss3651812972, ss3677013421, ss3739050700, ss3750519142, ss3878343013, ss3926987453, ss3984030572, ss3986573950, ss5206478604, ss5405844998, ss5653220223, ss5838010526, ss5848354855, ss5944582688	NC_000012.11:56744444:T:C	NC_000012.12:56350660:T:C	(self)
75995978, 28385927, 90155531, 9359334750, ss2190055824, ss3027416760, ss3693735542, ss3815849775, ss3972007926, ss4919456240, ss5290927765, ss5485665388, ss5588470043, ss5756318427, ss5813327007, ss5850395587, ss5904524057	NC_000012.12:56350660:T:C	NC_000012.12:56350660:T:C	(self)
ss16361216, ss76872924	NT_029419.12:18887750:T:C	NC_000012.12:56350660:T:C	(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 rs11575231

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
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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

rs11575231