Name: rs211131
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.

rs211131

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:17995970 (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=0.479674 (126965/264690, TOPMED)
T=0.479981 (67158/139918, GnomAD)
C=0.36804 (10400/28258, 14KJPN) (+ 19 more)
C=0.36753 (6159/16758, 8.3KJPN)
C=0.34552 (3809/11024, ALFA)
T=0.4577 (2931/6404, 1000G_30x)
T=0.4589 (2298/5008, 1000G)
C=0.4391 (1967/4480, Estonian)
C=0.4657 (1795/3854, ALSPAC)
C=0.4552 (1688/3708, TWINSUK)
C=0.3775 (1106/2930, KOREAN)
C=0.3603 (660/1832, Korea1K)
C=0.4014 (456/1136, Daghestan)
C=0.461 (460/998, GoNL)
C=0.475 (285/600, NorthernSweden)
C=0.444 (237/534, MGP)
T=0.315 (124/394, SGDP_PRJ)
T=0.469 (149/318, HapMap)
C=0.389 (84/216, Qatari)
C=0.472 (101/214, Vietnamese)
T=0.41 (18/44, Siberian)
C=0.47 (19/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SERGEF : 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	11024	T=0.65448	C=0.34552, G=0.00000
European	Sub	9538	T=0.6606	C=0.3394, G=0.0000
African	Sub	836	T=0.444	C=0.556, G=0.000
African Others	Sub	30	T=0.30	C=0.70, G=0.00
African American	Sub	806	T=0.449	C=0.551, G=0.000
Asian	Sub	48	T=0.94	C=0.06, G=0.00
East Asian	Sub	44	T=0.95	C=0.05, G=0.00
Other Asian	Sub	4	T=0.8	C=0.2, G=0.0
Latin American 1	Sub	24	T=1.00	C=0.00, G=0.00
Latin American 2	Sub	204	T=1.000	C=0.000, G=0.000
South Asian	Sub	20	T=0.85	C=0.15, G=0.00
Other	Sub	354	T=0.715	C=0.285, G=0.000

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
TopMed	Global	Study-wide	264690	T=0.479674	C=0.520326
gnomAD - Genomes	Global	Study-wide	139918	T=0.479981	C=0.520019
gnomAD - Genomes	European	Sub	75816	T=0.55141	C=0.44859
gnomAD - Genomes	African	Sub	41884	T=0.30379	C=0.69621
gnomAD - Genomes	American	Sub	13626	T=0.55842	C=0.44158
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	T=0.6596	C=0.3404
gnomAD - Genomes	East Asian	Sub	3122	T=0.5586	C=0.4414
gnomAD - Genomes	Other	Sub	2150	T=0.5047	C=0.4953
14KJPN	JAPANESE	Study-wide	28258	T=0.63196	C=0.36804
8.3KJPN	JAPANESE	Study-wide	16758	T=0.63247	C=0.36753
Allele Frequency Aggregator	Total	Global	11024	T=0.65448	C=0.34552, G=0.00000
Allele Frequency Aggregator	European	Sub	9538	T=0.6606	C=0.3394, G=0.0000
Allele Frequency Aggregator	African	Sub	836	T=0.444	C=0.556, G=0.000
Allele Frequency Aggregator	Other	Sub	354	T=0.715	C=0.285, G=0.000
Allele Frequency Aggregator	Latin American 2	Sub	204	T=1.000	C=0.000, G=0.000
Allele Frequency Aggregator	Asian	Sub	48	T=0.94	C=0.06, G=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	T=1.00	C=0.00, G=0.00
Allele Frequency Aggregator	South Asian	Sub	20	T=0.85	C=0.15, G=0.00
1000Genomes_30x	Global	Study-wide	6404	T=0.4577	C=0.5423
1000Genomes_30x	African	Sub	1786	T=0.2576	C=0.7424
1000Genomes_30x	Europe	Sub	1266	T=0.5561	C=0.4439
1000Genomes_30x	South Asian	Sub	1202	T=0.4268	C=0.5732
1000Genomes_30x	East Asian	Sub	1170	T=0.5915	C=0.4085
1000Genomes_30x	American	Sub	980	T=0.573	C=0.427
1000Genomes	Global	Study-wide	5008	T=0.4589	C=0.5411
1000Genomes	African	Sub	1322	T=0.2542	C=0.7458
1000Genomes	East Asian	Sub	1008	T=0.5952	C=0.4048
1000Genomes	Europe	Sub	1006	T=0.5547	C=0.4453
1000Genomes	South Asian	Sub	978	T=0.428	C=0.572
1000Genomes	American	Sub	694	T=0.555	C=0.445
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.5609	C=0.4391
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.5343	C=0.4657
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.5448	C=0.4552
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.6225	A=0.0000, C=0.3775
Korean Genome Project	KOREAN	Study-wide	1832	T=0.6397	C=0.3603
Genome-wide autozygosity in Daghestan	Global	Study-wide	1136	T=0.5986	C=0.4014
Genome-wide autozygosity in Daghestan	Daghestan	Sub	628	T=0.631	C=0.369
Genome-wide autozygosity in Daghestan	Near_East	Sub	144	T=0.597	C=0.403
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	T=0.574	C=0.426
Genome-wide autozygosity in Daghestan	Europe	Sub	108	T=0.574	C=0.426
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	T=0.44	C=0.56
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	T=0.64	C=0.36
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.539	C=0.461
Northern Sweden	ACPOP	Study-wide	600	T=0.525	C=0.475
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.556	C=0.444
SGDP_PRJ	Global	Study-wide	394	T=0.315	C=0.685
HapMap	Global	Study-wide	318	T=0.469	C=0.531
HapMap	African	Sub	118	T=0.297	C=0.703
HapMap	American	Sub	116	T=0.517	C=0.483
HapMap	Asian	Sub	84	T=0.64	C=0.36
Qatari	Global	Study-wide	216	T=0.611	C=0.389
A Vietnamese Genetic Variation Database	Global	Study-wide	214	T=0.528	C=0.472
Siberian	Global	Study-wide	44	T=0.41	C=0.59
The Danish reference pan genome	Danish	Study-wide	40	T=0.53	C=0.47

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 11	NC_000011.10:g.17995970T>A
GRCh38.p14 chr 11	NC_000011.10:g.17995970T>C
GRCh38.p14 chr 11	NC_000011.10:g.17995970T>G
GRCh37.p13 chr 11	NC_000011.9:g.18017517T>A
GRCh37.p13 chr 11	NC_000011.9:g.18017517T>C
GRCh37.p13 chr 11	NC_000011.9:g.18017517T>G

Gene: SERGEF, secretion regulating guanine nucleotide exchange factor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SERGEF transcript variant 1	NM_012139.4:c.509-61A>T	N/A	Intron Variant
SERGEF transcript variant 2	NR_104040.2:n.	N/A	Intron Variant
SERGEF transcript variant 3	NR_104041.2: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	G
GRCh38.p14 chr 11	NC_000011.10:g.17995970=	NC_000011.10:g.17995970T>A	NC_000011.10:g.17995970T>C	NC_000011.10:g.17995970T>G
GRCh37.p13 chr 11	NC_000011.9:g.18017517=	NC_000011.9:g.18017517T>A	NC_000011.9:g.18017517T>C	NC_000011.9:g.18017517T>G
SERGEF transcript	NM_012139.2:c.509-61=	NM_012139.2:c.509-61A>T	NM_012139.2:c.509-61A>G	NM_012139.2:c.509-61A>C
SERGEF transcript variant 1	NM_012139.4:c.509-61=	NM_012139.4:c.509-61A>T	NM_012139.4:c.509-61A>G	NM_012139.4:c.509-61A>C
SERGEF transcript variant X1	XM_005252852.1:c.167-61=	XM_005252852.1:c.167-61A>T	XM_005252852.1:c.167-61A>G	XM_005252852.1:c.167-61A>C
SERGEF transcript variant X2	XM_005252853.1:c.167-61=	XM_005252853.1:c.167-61A>T	XM_005252853.1:c.167-61A>G	XM_005252853.1:c.167-61A>C
SERGEF transcript variant X3	XM_005252854.1:c.167-61=	XM_005252854.1:c.167-61A>T	XM_005252854.1:c.167-61A>G	XM_005252854.1:c.167-61A>C
SERGEF transcript variant X4	XM_005252855.1:c.509-61=	XM_005252855.1:c.509-61A>T	XM_005252855.1:c.509-61A>G	XM_005252855.1:c.509-61A>C
SERGEF transcript variant X5	XM_005252856.1:c.167-61=	XM_005252856.1:c.167-61A>T	XM_005252856.1:c.167-61A>G	XM_005252856.1:c.167-61A>C

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#.

93 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KWOK	ss275985	Jul 12, 2000 (79)
2	SC_JCM	ss674668	Aug 11, 2000 (85)
3	KWOK	ss993487	Oct 04, 2000 (86)
4	KWOK	ss1832358	Oct 18, 2000 (87)
5	YUSUKE	ss2987961	Jun 15, 2001 (96)
6	SC_SNP	ss15490297	Feb 27, 2004 (120)
7	SSAHASNP	ss20744640	Apr 05, 2004 (121)
8	ABI	ss38785582	Mar 13, 2006 (126)
9	ILLUMINA	ss65749266	Oct 16, 2006 (127)
10	HGSV	ss80921474	Dec 15, 2007 (130)
11	HGSV	ss84036434	Dec 15, 2007 (130)
12	HGSV	ss86046894	Dec 15, 2007 (130)
13	BCMHGSC_JDW	ss88484603	Mar 23, 2008 (129)
14	HUMANGENOME_JCVI	ss97366810	Feb 04, 2009 (130)
15	BGI	ss102943371	Dec 01, 2009 (131)
16	1000GENOMES	ss114272289	Jan 25, 2009 (130)
17	ILLUMINA-UK	ss119705914	Dec 01, 2009 (131)
18	ENSEMBL	ss132328478	Dec 01, 2009 (131)
19	ENSEMBL	ss137791752	Dec 01, 2009 (131)
20	COMPLETE_GENOMICS	ss167927564	Jul 04, 2010 (132)
21	COMPLETE_GENOMICS	ss169218735	Jul 04, 2010 (132)
22	COMPLETE_GENOMICS	ss170573818	Jul 04, 2010 (132)
23	BUSHMAN	ss202445518	Jul 04, 2010 (132)
24	BCM-HGSC-SUB	ss207519107	Jul 04, 2010 (132)
25	1000GENOMES	ss225117684	Jul 14, 2010 (132)
26	1000GENOMES	ss235465885	Jul 15, 2010 (132)
27	1000GENOMES	ss242115518	Jul 15, 2010 (132)
28	BL	ss254931378	May 09, 2011 (134)
29	GMI	ss280903366	May 04, 2012 (137)
30	PJP	ss291189271	May 09, 2011 (134)
31	TISHKOFF	ss562416661	Apr 25, 2013 (138)
32	SSMP	ss657838836	Apr 25, 2013 (138)
33	EVA-GONL	ss988260461	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1077539581	Aug 21, 2014 (142)
35	1000GENOMES	ss1340313463	Aug 21, 2014 (142)
36	HAMMER_LAB	ss1397601171	Sep 08, 2015 (146)
37	DDI	ss1426552616	Apr 01, 2015 (144)
38	EVA_GENOME_DK	ss1575555628	Apr 01, 2015 (144)
39	EVA_DECODE	ss1597938702	Apr 01, 2015 (144)
40	EVA_UK10K_ALSPAC	ss1626095990	Apr 01, 2015 (144)
41	EVA_UK10K_TWINSUK	ss1669090023	Apr 01, 2015 (144)
42	EVA_MGP	ss1711285115	Apr 01, 2015 (144)
43	HAMMER_LAB	ss1806714988	Sep 08, 2015 (146)
44	WEILL_CORNELL_DGM	ss1931621386	Feb 12, 2016 (147)
45	GENOMED	ss1967304993	Jul 19, 2016 (147)
46	JJLAB	ss2026554950	Sep 14, 2016 (149)
47	USC_VALOUEV	ss2154843053	Dec 20, 2016 (150)
48	HUMAN_LONGEVITY	ss2180593894	Dec 20, 2016 (150)
49	SYSTEMSBIOZJU	ss2627747383	Nov 08, 2017 (151)
50	GRF	ss2699116376	Nov 08, 2017 (151)
51	GNOMAD	ss2896884235	Nov 08, 2017 (151)
52	SWEGEN	ss3007676989	Nov 08, 2017 (151)
53	BIOINF_KMB_FNS_UNIBA	ss3027073692	Nov 08, 2017 (151)
54	CSHL	ss3349476900	Nov 08, 2017 (151)
55	OMUKHERJEE_ADBS	ss3646423132	Oct 12, 2018 (152)
56	URBANLAB	ss3649545617	Oct 12, 2018 (152)
57	EGCUT_WGS	ss3675077220	Jul 13, 2019 (153)
58	EVA_DECODE	ss3691309824	Jul 13, 2019 (153)
59	ACPOP	ss3737963178	Jul 13, 2019 (153)
60	EVA	ss3749003474	Jul 13, 2019 (153)
61	PACBIO	ss3786881402	Jul 13, 2019 (153)
62	PACBIO	ss3792032896	Jul 13, 2019 (153)
63	PACBIO	ss3796914978	Jul 13, 2019 (153)
64	KHV_HUMAN_GENOMES	ss3814349841	Jul 13, 2019 (153)
65	EVA	ss3832504017	Apr 26, 2020 (154)
66	EVA	ss3839800188	Apr 26, 2020 (154)
67	EVA	ss3845276874	Apr 26, 2020 (154)
68	SGDP_PRJ	ss3875746689	Apr 26, 2020 (154)
69	KRGDB	ss3923986819	Apr 26, 2020 (154)
70	KOGIC	ss3969304405	Apr 26, 2020 (154)
71	FSA-LAB	ss3983997955	Apr 26, 2021 (155)
72	EVA	ss3986517990	Apr 26, 2021 (155)
73	TOPMED	ss4876927491	Apr 26, 2021 (155)
74	TOMMO_GENOMICS	ss5200900382	Apr 26, 2021 (155)
75	EVA	ss5237213358	Apr 26, 2021 (155)
76	1000G_HIGH_COVERAGE	ss5286571121	Oct 16, 2022 (156)
77	EVA	ss5398053962	Oct 16, 2022 (156)
78	HUGCELL_USP	ss5481857056	Oct 16, 2022 (156)
79	EVA	ss5510267315	Oct 16, 2022 (156)
80	1000G_HIGH_COVERAGE	ss5581782860	Oct 16, 2022 (156)
81	EVA	ss5623952652	Oct 16, 2022 (156)
82	EVA	ss5624018428	Oct 16, 2022 (156)
83	SANFORD_IMAGENETICS	ss5650732350	Oct 16, 2022 (156)
84	TOMMO_GENOMICS	ss5747715886	Oct 16, 2022 (156)
85	EVA	ss5800166643	Oct 16, 2022 (156)
86	YY_MCH	ss5812170292	Oct 16, 2022 (156)
87	EVA	ss5836328985	Oct 16, 2022 (156)
88	EVA	ss5848320065	Oct 16, 2022 (156)
89	EVA	ss5849878866	Oct 16, 2022 (156)
90	EVA	ss5919027360	Oct 16, 2022 (156)
91	EVA	ss5936547851	Oct 16, 2022 (156)
92	EVA	ss5942042466	Oct 16, 2022 (156)
93	EVA	ss5980663625	Oct 16, 2022 (156)
94	1000Genomes	NC_000011.9 - 18017517	Oct 12, 2018 (152)
95	1000Genomes_30x	NC_000011.10 - 17995970	Oct 16, 2022 (156)
96	The Avon Longitudinal Study of Parents and Children	NC_000011.9 - 18017517	Oct 12, 2018 (152)
97	Genome-wide autozygosity in Daghestan	NC_000011.8 - 17974093	Apr 26, 2020 (154)
98	Genetic variation in the Estonian population	NC_000011.9 - 18017517	Oct 12, 2018 (152)
99	The Danish reference pan genome	NC_000011.9 - 18017517	Apr 26, 2020 (154)
100	gnomAD - Genomes	NC_000011.10 - 17995970	Apr 26, 2021 (155)
101	Genome of the Netherlands Release 5	NC_000011.9 - 18017517	Apr 26, 2020 (154)
102	HapMap	NC_000011.10 - 17995970	Apr 26, 2020 (154)
103	KOREAN population from KRGDB	NC_000011.9 - 18017517	Apr 26, 2020 (154)
104	Korean Genome Project	NC_000011.10 - 17995970	Apr 26, 2020 (154)
105	Medical Genome Project healthy controls from Spanish population	NC_000011.9 - 18017517	Apr 26, 2020 (154)
106	Northern Sweden	NC_000011.9 - 18017517	Jul 13, 2019 (153)
107	Qatari	NC_000011.9 - 18017517	Apr 26, 2020 (154)
108	SGDP_PRJ	NC_000011.9 - 18017517	Apr 26, 2020 (154)
109	Siberian	NC_000011.9 - 18017517	Apr 26, 2020 (154)
110	8.3KJPN	NC_000011.9 - 18017517	Apr 26, 2021 (155)
111	14KJPN	NC_000011.10 - 17995970	Oct 16, 2022 (156)
112	TopMed	NC_000011.10 - 17995970	Apr 26, 2021 (155)
113	UK 10K study - Twins	NC_000011.9 - 18017517	Oct 12, 2018 (152)
114	A Vietnamese Genetic Variation Database	NC_000011.9 - 18017517	Jul 13, 2019 (153)
115	ALFA	NC_000011.10 - 17995970	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)
rs504641	Sep 19, 2000 (85)
rs58272432	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
31164213, ss3923986819	NC_000011.9:18017516:T:A	NC_000011.10:17995969:T:A	(self)
72467, ss80921474, ss84036434, ss86046894, ss88484603, ss114272289, ss119705914, ss167927564, ss169218735, ss170573818, ss202445518, ss207519107, ss254931378, ss280903366, ss291189271, ss1397601171, ss1597938702	NC_000011.8:17974092:T:C	NC_000011.10:17995969:T:C	(self)
52803078, 29332631, 20815468, 2464022, 13078190, 31164213, 400875, 11248043, 13663316, 27763669, 7359407, 58869689, 29332631, 6511281, ss225117684, ss235465885, ss242115518, ss562416661, ss657838836, ss988260461, ss1077539581, ss1340313463, ss1426552616, ss1575555628, ss1626095990, ss1669090023, ss1711285115, ss1806714988, ss1931621386, ss1967304993, ss2026554950, ss2154843053, ss2627747383, ss2699116376, ss2896884235, ss3007676989, ss3349476900, ss3646423132, ss3675077220, ss3737963178, ss3749003474, ss3786881402, ss3792032896, ss3796914978, ss3832504017, ss3839800188, ss3875746689, ss3923986819, ss3983997955, ss3986517990, ss5200900382, ss5398053962, ss5510267315, ss5623952652, ss5624018428, ss5650732350, ss5800166643, ss5836328985, ss5848320065, ss5936547851, ss5942042466, ss5980663625	NC_000011.9:18017516:T:C	NC_000011.10:17995969:T:C	(self)
69308795, 372769702, 560522, 25682406, 81552990, 92473147, 1822009430, ss2180593894, ss3027073692, ss3649545617, ss3691309824, ss3814349841, ss3845276874, ss3969304405, ss4876927491, ss5237213358, ss5286571121, ss5481857056, ss5581782860, ss5747715886, ss5812170292, ss5849878866, ss5919027360	NC_000011.10:17995969:T:C	NC_000011.10:17995969:T:C	(self)
ss15490297, ss20744640	NT_009237.16:16781456:T:C	NC_000011.10:17995969:T:C	(self)
ss275985, ss674668, ss993487, ss1832358, ss2987961, ss38785582, ss65749266, ss97366810, ss102943371, ss132328478, ss137791752	NT_009237.18:17957516:T:C	NC_000011.10:17995969:T:C	(self)
1822009430	NC_000011.10:17995969:T:G	NC_000011.10:17995969:T:G	(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 rs211131

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

rs211131