Name: rs6691873
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.

rs6691873

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:226577185 (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>C
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.094458 (25002/264690, TOPMED)
C=0.072049 (15054/208940, ALFA)
C=0.093200 (13065/140182, GnomAD) (+ 21 more)
C=0.12670 (3580/28256, 14KJPN)
C=0.12780 (2142/16760, 8.3KJPN)
C=0.1449 (928/6404, 1000G_30x)
C=0.1462 (732/5008, 1000G)
C=0.0592 (265/4480, Estonian)
C=0.0612 (236/3854, ALSPAC)
C=0.0653 (242/3708, TWINSUK)
C=0.1016 (297/2922, KOREAN)
C=0.1118 (233/2084, HGDP_Stanford)
C=0.1351 (255/1888, HapMap)
C=0.0977 (179/1832, Korea1K)
C=0.062 (62/998, GoNL)
C=0.050 (31/626, Chileans)
C=0.068 (41/600, NorthernSweden)
C=0.046 (10/216, Qatari)
C=0.125 (27/216, Vietnamese)
T=0.434 (59/136, SGDP_PRJ)
C=0.04 (2/48, Ancient Sardinia)
C=0.03 (1/40, GENOME_DK)
T=0.5 (4/8, Siberian)
C=0.5 (4/8, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: STUM : 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	208940	T=0.927951	C=0.072049
European	Sub	178012	T=0.935302	C=0.064698
African	Sub	7766	T=0.8356	C=0.1644
African Others	Sub	276	T=0.830	C=0.170
African American	Sub	7490	T=0.8358	C=0.1642
Asian	Sub	748	T=0.864	C=0.136
East Asian	Sub	572	T=0.881	C=0.119
Other Asian	Sub	176	T=0.807	C=0.193
Latin American 1	Sub	990	T=0.859	C=0.141
Latin American 2	Sub	9032	T=0.9464	C=0.0536
South Asian	Sub	5052	T=0.8112	C=0.1888
Other	Sub	7340	T=0.9210	C=0.0790

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=0.905542	C=0.094458
Allele Frequency Aggregator	Total	Global	208940	T=0.927951	C=0.072049
Allele Frequency Aggregator	European	Sub	178012	T=0.935302	C=0.064698
Allele Frequency Aggregator	Latin American 2	Sub	9032	T=0.9464	C=0.0536
Allele Frequency Aggregator	African	Sub	7766	T=0.8356	C=0.1644
Allele Frequency Aggregator	Other	Sub	7340	T=0.9210	C=0.0790
Allele Frequency Aggregator	South Asian	Sub	5052	T=0.8112	C=0.1888
Allele Frequency Aggregator	Latin American 1	Sub	990	T=0.859	C=0.141
Allele Frequency Aggregator	Asian	Sub	748	T=0.864	C=0.136
gnomAD - Genomes	Global	Study-wide	140182	T=0.906800	C=0.093200
gnomAD - Genomes	European	Sub	75918	T=0.93793	C=0.06207
gnomAD - Genomes	African	Sub	41998	T=0.83840	C=0.16160
gnomAD - Genomes	American	Sub	13666	T=0.93853	C=0.06147
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	T=0.9624	C=0.0376
gnomAD - Genomes	East Asian	Sub	3128	T=0.8756	C=0.1244
gnomAD - Genomes	Other	Sub	2150	T=0.9014	C=0.0986
14KJPN	JAPANESE	Study-wide	28256	T=0.87330	C=0.12670
8.3KJPN	JAPANESE	Study-wide	16760	T=0.87220	C=0.12780
1000Genomes_30x	Global	Study-wide	6404	T=0.8551	C=0.1449
1000Genomes_30x	African	Sub	1786	T=0.8046	C=0.1954
1000Genomes_30x	Europe	Sub	1266	T=0.9258	C=0.0742
1000Genomes_30x	South Asian	Sub	1202	T=0.7537	C=0.2463
1000Genomes_30x	East Asian	Sub	1170	T=0.8812	C=0.1188
1000Genomes_30x	American	Sub	980	T=0.949	C=0.051
1000Genomes	Global	Study-wide	5008	T=0.8538	C=0.1462
1000Genomes	African	Sub	1322	T=0.8018	C=0.1982
1000Genomes	East Asian	Sub	1008	T=0.8839	C=0.1161
1000Genomes	Europe	Sub	1006	T=0.9284	C=0.0716
1000Genomes	South Asian	Sub	978	T=0.754	C=0.246
1000Genomes	American	Sub	694	T=0.942	C=0.058
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.9408	C=0.0592
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.9388	C=0.0612
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.9347	C=0.0653
KOREAN population from KRGDB	KOREAN	Study-wide	2922	T=0.8984	C=0.1016
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	T=0.8882	C=0.1118
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	T=0.894	C=0.106
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	T=0.882	C=0.118
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	T=0.926	C=0.074
HGDP-CEPH-db Supplement 1	Europe	Sub	320	T=0.959	C=0.041
HGDP-CEPH-db Supplement 1	Africa	Sub	242	T=0.847	C=0.153
HGDP-CEPH-db Supplement 1	America	Sub	216	T=0.958	C=0.042
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	T=0.32	C=0.68
HapMap	Global	Study-wide	1888	T=0.8649	C=0.1351
HapMap	American	Sub	770	T=0.882	C=0.118
HapMap	African	Sub	688	T=0.818	C=0.182
HapMap	Asian	Sub	254	T=0.874	C=0.126
HapMap	Europe	Sub	176	T=0.960	C=0.040
Korean Genome Project	KOREAN	Study-wide	1832	T=0.9023	C=0.0977
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.938	C=0.062
Chileans	Chilean	Study-wide	626	T=0.950	C=0.050
Northern Sweden	ACPOP	Study-wide	600	T=0.932	C=0.068
Qatari	Global	Study-wide	216	T=0.954	C=0.046
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.875	C=0.125
SGDP_PRJ	Global	Study-wide	136	T=0.434	C=0.566
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	48	T=0.96	C=0.04
The Danish reference pan genome	Danish	Study-wide	40	T=0.97	C=0.03
Siberian	Global	Study-wide	8	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 1	NC_000001.11:g.226577185T>C
GRCh37.p13 chr 1	NC_000001.10:g.226764886T>C

Gene: STUM, stum, mechanosensory transduction mediator homolog (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
STUM transcript variant 1	NM_001003665.4:c.203-1961… NM_001003665.4:c.203-19617T>C	N/A	Intron Variant
STUM transcript variant X1	XM_011544183.4:c.203-1961… XM_011544183.4:c.203-19617T>C	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=	C
GRCh38.p14 chr 1	NC_000001.11:g.226577185=	NC_000001.11:g.226577185T>C
GRCh37.p13 chr 1	NC_000001.10:g.226764886=	NC_000001.10:g.226764886T>C
STUM transcript	NM_001003665.3:c.203-19617=	NM_001003665.3:c.203-19617T>C
STUM transcript variant 1	NM_001003665.4:c.203-19617=	NM_001003665.4:c.203-19617T>C
STUM transcript variant X1	XM_011544183.4:c.203-19617=	XM_011544183.4:c.203-19617T>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#.

106 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BCM_SSAHASNP	ss9880725	Jul 11, 2003 (116)
2	SC_SNP	ss15414077	Feb 27, 2004 (120)
3	AFFY	ss66200423	Nov 29, 2006 (127)
4	ILLUMINA	ss67485402	Nov 29, 2006 (127)
5	ILLUMINA	ss67843297	Nov 29, 2006 (127)
6	ILLUMINA	ss68256836	Dec 12, 2006 (127)
7	ILLUMINA	ss70879919	May 24, 2008 (130)
8	ILLUMINA	ss71470414	May 16, 2007 (127)
9	ILLUMINA	ss75476710	Dec 07, 2007 (129)
10	AFFY	ss76287184	Dec 07, 2007 (129)
11	KRIBB_YJKIM	ss84524635	Dec 14, 2007 (130)
12	HGSV	ss85665603	Dec 14, 2007 (130)
13	1000GENOMES	ss111871014	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss119230155	Feb 15, 2009 (130)
15	ILLUMINA	ss154375613	Dec 01, 2009 (131)
16	GMI	ss156366550	Dec 01, 2009 (131)
17	ILLUMINA	ss159551490	Dec 01, 2009 (131)
18	ILLUMINA	ss160798611	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss165305099	Jul 04, 2010 (132)
20	AFFY	ss173130368	Jul 04, 2010 (132)
21	ILLUMINA	ss174071264	Jul 04, 2010 (132)
22	BCM-HGSC-SUB	ss205248291	Jul 04, 2010 (132)
23	1000GENOMES	ss218916806	Jul 14, 2010 (132)
24	1000GENOMES	ss230929451	Jul 14, 2010 (132)
25	1000GENOMES	ss238537166	Jul 15, 2010 (132)
26	BL	ss253868713	May 09, 2011 (134)
27	GMI	ss276244734	May 04, 2012 (137)
28	ILLUMINA	ss410942746	Sep 17, 2011 (135)
29	ILLUMINA	ss481319225	May 04, 2012 (137)
30	ILLUMINA	ss481344374	May 04, 2012 (137)
31	ILLUMINA	ss482326052	Sep 08, 2015 (146)
32	ILLUMINA	ss485454772	May 04, 2012 (137)
33	ILLUMINA	ss537379180	Sep 08, 2015 (146)
34	TISHKOFF	ss555179796	Apr 25, 2013 (138)
35	SSMP	ss648751564	Apr 25, 2013 (138)
36	ILLUMINA	ss778947980	Aug 21, 2014 (142)
37	ILLUMINA	ss783172848	Aug 21, 2014 (142)
38	ILLUMINA	ss784128336	Aug 21, 2014 (142)
39	ILLUMINA	ss832432405	Apr 01, 2015 (144)
40	ILLUMINA	ss833062663	Aug 21, 2014 (142)
41	ILLUMINA	ss833653491	Aug 21, 2014 (142)
42	ILLUMINA	ss834409795	Aug 21, 2014 (142)
43	EVA-GONL	ss976215207	Aug 21, 2014 (142)
44	JMKIDD_LAB	ss1068655026	Aug 21, 2014 (142)
45	1000GENOMES	ss1294917220	Aug 21, 2014 (142)
46	EVA_GENOME_DK	ss1574722885	Apr 01, 2015 (144)
47	EVA_DECODE	ss1585613087	Apr 01, 2015 (144)
48	EVA_UK10K_ALSPAC	ss1602282413	Apr 01, 2015 (144)
49	EVA_UK10K_TWINSUK	ss1645276446	Apr 01, 2015 (144)
50	EVA_SVP	ss1712410554	Apr 01, 2015 (144)
51	ILLUMINA	ss1751902394	Sep 08, 2015 (146)
52	HAMMER_LAB	ss1795820132	Sep 08, 2015 (146)
53	WEILL_CORNELL_DGM	ss1919437114	Feb 12, 2016 (147)
54	JJLAB	ss2020243083	Sep 14, 2016 (149)
55	USC_VALOUEV	ss2148277544	Dec 20, 2016 (150)
56	HUMAN_LONGEVITY	ss2170640277	Dec 20, 2016 (150)
57	SYSTEMSBIOZJU	ss2624632921	Nov 08, 2017 (151)
58	ILLUMINA	ss2632637831	Nov 08, 2017 (151)
59	GRF	ss2698275733	Nov 08, 2017 (151)
60	GNOMAD	ss2766979882	Nov 08, 2017 (151)
61	SWEGEN	ss2988561529	Nov 08, 2017 (151)
62	BIOINF_KMB_FNS_UNIBA	ss3023882005	Nov 08, 2017 (151)
63	CSHL	ss3343943601	Nov 08, 2017 (151)
64	ILLUMINA	ss3626323719	Oct 11, 2018 (152)
65	ILLUMINA	ss3630667222	Oct 11, 2018 (152)
66	ILLUMINA	ss3632927968	Oct 11, 2018 (152)
67	ILLUMINA	ss3633624106	Oct 11, 2018 (152)
68	ILLUMINA	ss3634376252	Oct 11, 2018 (152)
69	ILLUMINA	ss3635317155	Oct 11, 2018 (152)
70	ILLUMINA	ss3636055138	Oct 11, 2018 (152)
71	ILLUMINA	ss3637067706	Oct 11, 2018 (152)
72	ILLUMINA	ss3637818002	Oct 11, 2018 (152)
73	ILLUMINA	ss3638924130	Oct 11, 2018 (152)
74	ILLUMINA	ss3639773784	Oct 11, 2018 (152)
75	ILLUMINA	ss3640083605	Oct 11, 2018 (152)
76	ILLUMINA	ss3642824079	Oct 11, 2018 (152)
77	ILLUMINA	ss3643826901	Oct 11, 2018 (152)
78	EGCUT_WGS	ss3656520675	Jul 12, 2019 (153)
79	EVA_DECODE	ss3688761076	Jul 12, 2019 (153)
80	ACPOP	ss3727921174	Jul 12, 2019 (153)
81	ILLUMINA	ss3744677105	Jul 12, 2019 (153)
82	EVA	ss3747419218	Jul 12, 2019 (153)
83	ILLUMINA	ss3772177997	Jul 12, 2019 (153)
84	KHV_HUMAN_GENOMES	ss3800421905	Jul 12, 2019 (153)
85	EVA	ss3826678773	Apr 25, 2020 (154)
86	HGDP	ss3847365637	Apr 25, 2020 (154)
87	SGDP_PRJ	ss3851037263	Apr 25, 2020 (154)
88	KRGDB	ss3896374784	Apr 25, 2020 (154)
89	KOGIC	ss3946629713	Apr 25, 2020 (154)
90	EVA	ss3984856179	Apr 25, 2021 (155)
91	EVA	ss4016965858	Apr 25, 2021 (155)
92	TOPMED	ss4485942593	Apr 25, 2021 (155)
93	TOMMO_GENOMICS	ss5148740932	Apr 25, 2021 (155)
94	1000G_HIGH_COVERAGE	ss5246030185	Oct 12, 2022 (156)
95	EVA	ss5314687548	Oct 12, 2022 (156)
96	EVA	ss5325217800	Oct 12, 2022 (156)
97	HUGCELL_USP	ss5446442017	Oct 12, 2022 (156)
98	1000G_HIGH_COVERAGE	ss5520246557	Oct 12, 2022 (156)
99	SANFORD_IMAGENETICS	ss5627579634	Oct 12, 2022 (156)
100	TOMMO_GENOMICS	ss5676589255	Oct 12, 2022 (156)
101	EVA	ss5799513738	Oct 12, 2022 (156)
102	YY_MCH	ss5801698783	Oct 12, 2022 (156)
103	EVA	ss5833356845	Oct 12, 2022 (156)
104	EVA	ss5849315475	Oct 12, 2022 (156)
105	EVA	ss5912241681	Oct 12, 2022 (156)
106	EVA	ss5939423976	Oct 12, 2022 (156)
107	1000Genomes	NC_000001.10 - 226764886	Oct 11, 2018 (152)
108	1000Genomes_30x	NC_000001.11 - 226577185	Oct 12, 2022 (156)
109	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 226764886	Oct 11, 2018 (152)
110	Chileans	NC_000001.10 - 226764886	Apr 25, 2020 (154)
111	Genetic variation in the Estonian population	NC_000001.10 - 226764886	Oct 11, 2018 (152)
112	The Danish reference pan genome	NC_000001.10 - 226764886	Apr 25, 2020 (154)
113	gnomAD - Genomes	NC_000001.11 - 226577185	Apr 25, 2021 (155)
114	Genome of the Netherlands Release 5	NC_000001.10 - 226764886	Apr 25, 2020 (154)
115	HGDP-CEPH-db Supplement 1	NC_000001.9 - 224831509	Apr 25, 2020 (154)
116	HapMap	NC_000001.11 - 226577185	Apr 25, 2020 (154)
117	KOREAN population from KRGDB	NC_000001.10 - 226764886	Apr 25, 2020 (154)
118	Korean Genome Project	NC_000001.11 - 226577185	Apr 25, 2020 (154)
119	Northern Sweden	NC_000001.10 - 226764886	Jul 12, 2019 (153)
120	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 226764886	Apr 25, 2021 (155)
121	Qatari	NC_000001.10 - 226764886	Apr 25, 2020 (154)
122	SGDP_PRJ	NC_000001.10 - 226764886	Apr 25, 2020 (154)
123	Siberian	NC_000001.10 - 226764886	Apr 25, 2020 (154)
124	8.3KJPN	NC_000001.10 - 226764886	Apr 25, 2021 (155)
125	14KJPN	NC_000001.11 - 226577185	Oct 12, 2022 (156)
126	TopMed	NC_000001.11 - 226577185	Apr 25, 2021 (155)
127	UK 10K study - Twins	NC_000001.10 - 226764886	Oct 11, 2018 (152)
128	A Vietnamese Genetic Variation Database	NC_000001.10 - 226764886	Jul 12, 2019 (153)
129	ALFA	NC_000001.11 - 226577185	Apr 25, 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)
rs57810931	May 24, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss85665603, ss3638924130, ss3639773784, ss3643826901	NC_000001.8:223071620:T:C	NC_000001.11:226577184:T:C	(self)
43529, ss111871014, ss119230155, ss160798611, ss165305099, ss205248291, ss253868713, ss276244734, ss410942746, ss481319225, ss1585613087, ss1712410554, ss3642824079, ss3847365637	NC_000001.9:224831508:T:C	NC_000001.11:226577184:T:C	(self)
5781475, 3195562, 34792, 2258923, 1913724, 1396504, 3552178, 1206039, 82106, 1479044, 3054243, 793898, 6710239, 3195562, 694087, ss218916806, ss230929451, ss238537166, ss481344374, ss482326052, ss485454772, ss537379180, ss555179796, ss648751564, ss778947980, ss783172848, ss784128336, ss832432405, ss833062663, ss833653491, ss834409795, ss976215207, ss1068655026, ss1294917220, ss1574722885, ss1602282413, ss1645276446, ss1751902394, ss1795820132, ss1919437114, ss2020243083, ss2148277544, ss2624632921, ss2632637831, ss2698275733, ss2766979882, ss2988561529, ss3343943601, ss3626323719, ss3630667222, ss3632927968, ss3633624106, ss3634376252, ss3635317155, ss3636055138, ss3637067706, ss3637818002, ss3640083605, ss3656520675, ss3727921174, ss3744677105, ss3747419218, ss3772177997, ss3826678773, ss3851037263, ss3896374784, ss3984856179, ss4016965858, ss5148740932, ss5314687548, ss5325217800, ss5627579634, ss5799513738, ss5833356845, ss5939423976	NC_000001.10:226764885:T:C	NC_000001.11:226577184:T:C	(self)
7772492, 41523014, 282485, 3007714, 10426359, 49548928, 3816432444, ss2170640277, ss3023882005, ss3688761076, ss3800421905, ss3946629713, ss4485942593, ss5246030185, ss5446442017, ss5520246557, ss5676589255, ss5801698783, ss5849315475, ss5912241681	NC_000001.11:226577184:T:C	NC_000001.11:226577184:T:C	(self)
ss9880725	NT_004559.10:278203:T:C	NC_000001.11:226577184:T:C	(self)
ss15414077	NT_004559.11:2941079:T:C	NC_000001.11:226577184:T:C	(self)
ss66200423, ss67485402, ss67843297, ss68256836, ss70879919, ss71470414, ss75476710, ss76287184, ss84524635, ss154375613, ss156366550, ss159551490, ss173130368, ss174071264	NT_167186.1:20282664:T:C	NC_000001.11:226577184: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 rs6691873

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

rs6691873