Name: rs937351
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.

rs937351

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr8:26773220 (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: C>A / C>G / C>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.438638 (116103/264690, TOPMED)
C=0.457658 (64073/140002, GnomAD)
C=0.13685 (3867/28258, 14KJPN) (+ 17 more)
C=0.49647 (12089/24350, ALFA)
C=0.13705 (2297/16760, 8.3KJPN)
C=0.3698 (2368/6404, 1000G_30x)
C=0.3660 (1833/5008, 1000G)
T=0.4478 (2006/4480, Estonian)
T=0.4497 (1733/3854, ALSPAC)
T=0.4458 (1653/3708, TWINSUK)
C=0.1266 (371/2930, KOREAN)
C=0.3286 (621/1890, HapMap)
C=0.1381 (253/1832, Korea1K)
T=0.431 (430/998, GoNL)
T=0.463 (278/600, NorthernSweden)
C=0.244 (114/468, SGDP_PRJ)
C=0.440 (95/216, Qatari)
C=0.118 (25/212, Vietnamese)
T=0.35 (14/40, GENOME_DK)
C=0.21 (7/34, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADRA1A : 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	24350	C=0.49647	T=0.50353
European	Sub	18126	C=0.54706	T=0.45294
African	Sub	4114	C=0.2856	T=0.7144
African Others	Sub	148	C=0.270	T=0.730
African American	Sub	3966	C=0.2862	T=0.7138
Asian	Sub	124	C=0.097	T=0.903
East Asian	Sub	96	C=0.10	T=0.90
Other Asian	Sub	28	C=0.07	T=0.93
Latin American 1	Sub	168	C=0.458	T=0.542
Latin American 2	Sub	670	C=0.510	T=0.490
South Asian	Sub	98	C=0.47	T=0.53
Other	Sub	1050	C=0.4962	T=0.5038

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	C=0.438638	T=0.561362
gnomAD - Genomes	Global	Study-wide	140002	C=0.457658	T=0.542342
gnomAD - Genomes	European	Sub	75820	C=0.56163	T=0.43837
gnomAD - Genomes	African	Sub	41940	C=0.29301	T=0.70699
gnomAD - Genomes	American	Sub	13648	C=0.46197	T=0.53803
gnomAD - Genomes	Ashkenazi Jewish	Sub	3318	C=0.5072	T=0.4928
gnomAD - Genomes	East Asian	Sub	3130	C=0.0843	T=0.9157
gnomAD - Genomes	Other	Sub	2146	C=0.4422	T=0.5578
14KJPN	JAPANESE	Study-wide	28258	C=0.13685	T=0.86315
Allele Frequency Aggregator	Total	Global	24350	C=0.49647	T=0.50353
Allele Frequency Aggregator	European	Sub	18126	C=0.54706	T=0.45294
Allele Frequency Aggregator	African	Sub	4114	C=0.2856	T=0.7144
Allele Frequency Aggregator	Other	Sub	1050	C=0.4962	T=0.5038
Allele Frequency Aggregator	Latin American 2	Sub	670	C=0.510	T=0.490
Allele Frequency Aggregator	Latin American 1	Sub	168	C=0.458	T=0.542
Allele Frequency Aggregator	Asian	Sub	124	C=0.097	T=0.903
Allele Frequency Aggregator	South Asian	Sub	98	C=0.47	T=0.53
8.3KJPN	JAPANESE	Study-wide	16760	C=0.13705	T=0.86295
1000Genomes_30x	Global	Study-wide	6404	C=0.3698	T=0.6302
1000Genomes_30x	African	Sub	1786	C=0.2648	T=0.7352
1000Genomes_30x	Europe	Sub	1266	C=0.5711	T=0.4289
1000Genomes_30x	South Asian	Sub	1202	C=0.4642	T=0.5358
1000Genomes_30x	East Asian	Sub	1170	C=0.1009	T=0.8991
1000Genomes_30x	American	Sub	980	C=0.506	T=0.494
1000Genomes	Global	Study-wide	5008	C=0.3660	T=0.6340
1000Genomes	African	Sub	1322	C=0.2655	T=0.7345
1000Genomes	East Asian	Sub	1008	C=0.1062	T=0.8938
1000Genomes	Europe	Sub	1006	C=0.5686	T=0.4314
1000Genomes	South Asian	Sub	978	C=0.457	T=0.543
1000Genomes	American	Sub	694	C=0.513	T=0.487
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.5522	T=0.4478
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.5503	T=0.4497
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.5542	T=0.4458
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.1266	A=0.0000, G=0.0000, T=0.8734
HapMap	Global	Study-wide	1890	C=0.3286	T=0.6714
HapMap	American	Sub	770	C=0.410	T=0.590
HapMap	African	Sub	690	C=0.251	T=0.749
HapMap	Asian	Sub	254	C=0.138	T=0.862
HapMap	Europe	Sub	176	C=0.551	T=0.449
Korean Genome Project	KOREAN	Study-wide	1832	C=0.1381	T=0.8619
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.569	T=0.431
Northern Sweden	ACPOP	Study-wide	600	C=0.537	T=0.463
SGDP_PRJ	Global	Study-wide	468	C=0.244	T=0.756
Qatari	Global	Study-wide	216	C=0.440	T=0.560
A Vietnamese Genetic Variation Database	Global	Study-wide	212	C=0.118	T=0.882
The Danish reference pan genome	Danish	Study-wide	40	C=0.65	T=0.35
Siberian	Global	Study-wide	34	C=0.21	T=0.79

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 8	NC_000008.11:g.26773220C>A
GRCh38.p14 chr 8	NC_000008.11:g.26773220C>G
GRCh38.p14 chr 8	NC_000008.11:g.26773220C>T
GRCh37.p13 chr 8	NC_000008.10:g.26630737C>A
GRCh37.p13 chr 8	NC_000008.10:g.26630737C>G
GRCh37.p13 chr 8	NC_000008.10:g.26630737C>T
ADRA1A RefSeqGene	NG_029395.1:g.97186G>T
ADRA1A RefSeqGene	NG_029395.1:g.97186G>C
ADRA1A RefSeqGene	NG_029395.1:g.97186G>A

Gene: ADRA1A, adrenoceptor alpha 1A (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADRA1A transcript variant 1	NM_000680.4:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant 5	NM_001322502.1:c.884-1644… NM_001322502.1:c.884-16441G>T	N/A	Intron Variant
ADRA1A transcript variant 6	NM_001322503.1:c.884-2447… NM_001322503.1:c.884-24472G>T	N/A	Intron Variant
ADRA1A transcript variant 3	NM_033302.3:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant 2	NM_033303.4:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant 4	NM_033304.3:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant 7	NM_001322504.1:c.	N/A	Genic Downstream Transcript Variant
ADRA1A transcript variant 8	NR_136343.1:n.	N/A	Intron Variant
ADRA1A transcript variant X3	XM_006716293.5:c.884-2554… XM_006716293.5:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant X1	XM_017013094.2:c.884-2554… XM_017013094.2:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant X2	XM_017013095.2:c.884-2554… XM_017013095.2:c.884-2554G>T	N/A	Intron Variant
ADRA1A transcript variant X5	XM_011544412.4:c.	N/A	Genic Downstream Transcript Variant
ADRA1A transcript variant X4	XM_017013096.2:c.	N/A	Genic Downstream 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	C=	A	G	T
GRCh38.p14 chr 8	NC_000008.11:g.26773220=	NC_000008.11:g.26773220C>A	NC_000008.11:g.26773220C>G	NC_000008.11:g.26773220C>T
GRCh37.p13 chr 8	NC_000008.10:g.26630737=	NC_000008.10:g.26630737C>A	NC_000008.10:g.26630737C>G	NC_000008.10:g.26630737C>T
ADRA1A RefSeqGene	NG_029395.1:g.97186=	NG_029395.1:g.97186G>T	NG_029395.1:g.97186G>C	NG_029395.1:g.97186G>A
ADRA1A transcript variant 1	NM_000680.2:c.884-2554=	NM_000680.2:c.884-2554G>T	NM_000680.2:c.884-2554G>C	NM_000680.2:c.884-2554G>A
ADRA1A transcript variant 1	NM_000680.4:c.884-2554=	NM_000680.4:c.884-2554G>T	NM_000680.4:c.884-2554G>C	NM_000680.4:c.884-2554G>A
ADRA1A transcript variant 5	NM_001322502.1:c.884-16441=	NM_001322502.1:c.884-16441G>T	NM_001322502.1:c.884-16441G>C	NM_001322502.1:c.884-16441G>A
ADRA1A transcript variant 6	NM_001322503.1:c.884-24472=	NM_001322503.1:c.884-24472G>T	NM_001322503.1:c.884-24472G>C	NM_001322503.1:c.884-24472G>A
ADRA1A transcript variant 3	NM_033302.2:c.884-2554=	NM_033302.2:c.884-2554G>T	NM_033302.2:c.884-2554G>C	NM_033302.2:c.884-2554G>A
ADRA1A transcript variant 3	NM_033302.3:c.884-2554=	NM_033302.3:c.884-2554G>T	NM_033302.3:c.884-2554G>C	NM_033302.3:c.884-2554G>A
ADRA1A transcript variant 2	NM_033303.3:c.884-2554=	NM_033303.3:c.884-2554G>T	NM_033303.3:c.884-2554G>C	NM_033303.3:c.884-2554G>A
ADRA1A transcript variant 2	NM_033303.4:c.884-2554=	NM_033303.4:c.884-2554G>T	NM_033303.4:c.884-2554G>C	NM_033303.4:c.884-2554G>A
ADRA1A transcript variant 4	NM_033304.2:c.884-2554=	NM_033304.2:c.884-2554G>T	NM_033304.2:c.884-2554G>C	NM_033304.2:c.884-2554G>A
ADRA1A transcript variant 4	NM_033304.3:c.884-2554=	NM_033304.3:c.884-2554G>T	NM_033304.3:c.884-2554G>C	NM_033304.3:c.884-2554G>A
ADRA1A transcript variant X1	XM_005273414.1:c.884-2554=	XM_005273414.1:c.884-2554G>T	XM_005273414.1:c.884-2554G>C	XM_005273414.1:c.884-2554G>A
ADRA1A transcript variant X3	XM_006716293.5:c.884-2554=	XM_006716293.5:c.884-2554G>T	XM_006716293.5:c.884-2554G>C	XM_006716293.5:c.884-2554G>A
ADRA1A transcript variant X1	XM_017013094.2:c.884-2554=	XM_017013094.2:c.884-2554G>T	XM_017013094.2:c.884-2554G>C	XM_017013094.2:c.884-2554G>A
ADRA1A transcript variant X2	XM_017013095.2:c.884-2554=	XM_017013095.2:c.884-2554G>T	XM_017013095.2:c.884-2554G>C	XM_017013095.2:c.884-2554G>A

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#.

83 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	TSC-CSHL	ss1377254	Oct 05, 2000 (86)
2	TSC-CSHL	ss5528596	Oct 08, 2002 (108)
3	SC_JCM	ss5856188	Feb 20, 2003 (111)
4	WI_SSAHASNP	ss14323557	Dec 05, 2003 (119)
5	CSHL-HAPMAP	ss19755897	Feb 27, 2004 (120)
6	ABI	ss43202513	Mar 15, 2006 (126)
7	ILLUMINA	ss65788364	Oct 14, 2006 (127)
8	ILLUMINA	ss74989763	Dec 07, 2007 (129)
9	HGSV	ss82927817	Dec 14, 2007 (130)
10	RSG_JCVI	ss86216385	Mar 23, 2008 (129)
11	BCMHGSC_JDW	ss93859862	Mar 25, 2008 (129)
12	BGI	ss105608069	Feb 02, 2009 (130)
13	1000GENOMES	ss112933317	Jan 25, 2009 (130)
14	ILLUMINA-UK	ss115874329	Feb 14, 2009 (130)
15	KRIBB_YJKIM	ss119374505	Dec 01, 2009 (131)
16	ENSEMBL	ss143354089	Dec 01, 2009 (131)
17	GMI	ss156178346	Dec 01, 2009 (131)
18	ENSEMBL	ss161633597	Dec 01, 2009 (131)
19	COMPLETE_GENOMICS	ss162267445	Jul 04, 2010 (132)
20	COMPLETE_GENOMICS	ss164246705	Jul 04, 2010 (132)
21	ILLUMINA	ss174827493	Jul 04, 2010 (132)
22	BUSHMAN	ss198954705	Jul 04, 2010 (132)
23	1000GENOMES	ss210496627	Jul 14, 2010 (132)
24	1000GENOMES	ss223616393	Jul 14, 2010 (132)
25	1000GENOMES	ss234374938	Jul 15, 2010 (132)
26	1000GENOMES	ss241244668	Jul 15, 2010 (132)
27	BL	ss254211506	May 09, 2011 (134)
28	GMI	ss279744605	May 04, 2012 (137)
29	PJP	ss294244686	May 09, 2011 (134)
30	ILLUMINA	ss537592335	Sep 08, 2015 (146)
31	TISHKOFF	ss560637622	Apr 25, 2013 (138)
32	SSMP	ss655072278	Apr 25, 2013 (138)
33	EVA-GONL	ss985330087	Aug 21, 2014 (142)
34	JMKIDD_LAB	ss1075383256	Aug 21, 2014 (142)
35	1000GENOMES	ss1329132138	Aug 21, 2014 (142)
36	DDI	ss1431459510	Apr 01, 2015 (144)
37	EVA_GENOME_DK	ss1582616590	Apr 01, 2015 (144)
38	EVA_DECODE	ss1594922896	Apr 01, 2015 (144)
39	EVA_UK10K_ALSPAC	ss1620252037	Apr 01, 2015 (144)
40	EVA_UK10K_TWINSUK	ss1663246070	Apr 01, 2015 (144)
41	EVA_SVP	ss1713025615	Apr 01, 2015 (144)
42	HAMMER_LAB	ss1805459077	Sep 08, 2015 (146)
43	WEILL_CORNELL_DGM	ss1928619306	Feb 12, 2016 (147)
44	GENOMED	ss1970943259	Jul 19, 2016 (147)
45	JJLAB	ss2025011655	Sep 14, 2016 (149)
46	USC_VALOUEV	ss2153233643	Dec 20, 2016 (150)
47	HUMAN_LONGEVITY	ss2301740853	Dec 20, 2016 (150)
48	SYSTEMSBIOZJU	ss2626989458	Nov 08, 2017 (151)
49	GRF	ss2708995417	Nov 08, 2017 (151)
50	GNOMAD	ss2864696846	Nov 08, 2017 (151)
51	SWEGEN	ss3002890253	Nov 08, 2017 (151)
52	BIOINF_KMB_FNS_UNIBA	ss3026296788	Nov 08, 2017 (151)
53	CSHL	ss3348106494	Nov 08, 2017 (151)
54	ILLUMINA	ss3630027105	Oct 12, 2018 (152)
55	ILLUMINA	ss3638751649	Oct 12, 2018 (152)
56	ILLUMINA	ss3643683194	Oct 12, 2018 (152)
57	URBANLAB	ss3648880259	Oct 12, 2018 (152)
58	EGCUT_WGS	ss3670574158	Jul 13, 2019 (153)
59	EVA_DECODE	ss3721666685	Jul 13, 2019 (153)
60	ACPOP	ss3735514885	Jul 13, 2019 (153)
61	EVA	ss3767786478	Jul 13, 2019 (153)
62	KHV_HUMAN_GENOMES	ss3810948137	Jul 13, 2019 (153)
63	EVA	ss3831083091	Apr 26, 2020 (154)
64	EVA	ss3839050581	Apr 26, 2020 (154)
65	EVA	ss3844508828	Apr 26, 2020 (154)
66	SGDP_PRJ	ss3869551844	Apr 26, 2020 (154)
67	KRGDB	ss3916986668	Apr 26, 2020 (154)
68	KOGIC	ss3963513176	Apr 26, 2020 (154)
69	EVA	ss4017382858	Apr 26, 2021 (155)
70	TOPMED	ss4779913291	Apr 26, 2021 (155)
71	TOMMO_GENOMICS	ss5187894938	Apr 26, 2021 (155)
72	1000G_HIGH_COVERAGE	ss5276520285	Oct 16, 2022 (156)
73	EVA	ss5379993157	Oct 16, 2022 (156)
74	HUGCELL_USP	ss5473153357	Oct 16, 2022 (156)
75	EVA	ss5509292587	Oct 16, 2022 (156)
76	1000G_HIGH_COVERAGE	ss5566537193	Oct 16, 2022 (156)
77	SANFORD_IMAGENETICS	ss5645032471	Oct 16, 2022 (156)
78	TOMMO_GENOMICS	ss5729582264	Oct 16, 2022 (156)
79	YY_MCH	ss5809563066	Oct 16, 2022 (156)
80	EVA	ss5830298390	Oct 16, 2022 (156)
81	EVA	ss5856310384	Oct 16, 2022 (156)
82	EVA	ss5888242926	Oct 16, 2022 (156)
83	EVA	ss5974218131	Oct 16, 2022 (156)
84	1000Genomes	NC_000008.10 - 26630737	Oct 12, 2018 (152)
85	1000Genomes_30x	NC_000008.11 - 26773220	Oct 16, 2022 (156)
86	The Avon Longitudinal Study of Parents and Children	NC_000008.10 - 26630737	Oct 12, 2018 (152)
87	Genetic variation in the Estonian population	NC_000008.10 - 26630737	Oct 12, 2018 (152)
88	The Danish reference pan genome	NC_000008.10 - 26630737	Apr 26, 2020 (154)
89	gnomAD - Genomes	NC_000008.11 - 26773220	Apr 26, 2021 (155)
90	Genome of the Netherlands Release 5	NC_000008.10 - 26630737	Apr 26, 2020 (154)
91	HapMap	NC_000008.11 - 26773220	Apr 26, 2020 (154)
92	KOREAN population from KRGDB	NC_000008.10 - 26630737	Apr 26, 2020 (154)
93	Korean Genome Project	NC_000008.11 - 26773220	Apr 26, 2020 (154)
94	Northern Sweden	NC_000008.10 - 26630737	Jul 13, 2019 (153)
95	Qatari	NC_000008.10 - 26630737	Apr 26, 2020 (154)
96	SGDP_PRJ	NC_000008.10 - 26630737	Apr 26, 2020 (154)
97	Siberian	NC_000008.10 - 26630737	Apr 26, 2020 (154)
98	8.3KJPN	NC_000008.10 - 26630737	Apr 26, 2021 (155)
99	14KJPN	NC_000008.11 - 26773220	Oct 16, 2022 (156)
100	TopMed	NC_000008.11 - 26773220	Apr 26, 2021 (155)
101	UK 10K study - Twins	NC_000008.10 - 26630737	Oct 12, 2018 (152)
102	A Vietnamese Genetic Variation Database	NC_000008.10 - 26630737	Jul 13, 2019 (153)
103	ALFA	NC_000008.11 - 26773220	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)
rs56710842	May 23, 2008 (130)
rs386622170	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
24164062, ss3916986668	NC_000008.10:26630736:C:A	NC_000008.11:26773219:C:A	(self)
24164062, ss3916986668	NC_000008.10:26630736:C:G	NC_000008.11:26773219:C:G	(self)
ss82927817, ss93859862, ss112933317, ss115874329, ss162267445, ss164246705, ss198954705, ss210496627, ss254211506, ss279744605, ss294244686, ss1594922896, ss1713025615, ss3643683194	NC_000008.9:26686653:C:T	NC_000008.11:26773219:C:T	(self)
41233771, 22926071, 16312406, 8781528, 10242882, 24164062, 8799750, 10661236, 21568824, 5749997, 45864245, 22926071, 5111598, ss223616393, ss234374938, ss241244668, ss537592335, ss560637622, ss655072278, ss985330087, ss1075383256, ss1329132138, ss1431459510, ss1582616590, ss1620252037, ss1663246070, ss1805459077, ss1928619306, ss1970943259, ss2025011655, ss2153233643, ss2626989458, ss2708995417, ss2864696846, ss3002890253, ss3348106494, ss3630027105, ss3638751649, ss3670574158, ss3735514885, ss3767786478, ss3831083091, ss3839050581, ss3869551844, ss3916986668, ss4017382858, ss5187894938, ss5379993157, ss5509292587, ss5645032471, ss5830298390, ss5974218131	NC_000008.10:26630736:C:T	NC_000008.11:26773219:C:T	(self)
54063128, 290740649, 3591691, 19891177, 63419368, 617290851, 4166226463, ss2301740853, ss3026296788, ss3648880259, ss3721666685, ss3810948137, ss3844508828, ss3963513176, ss4779913291, ss5276520285, ss5473153357, ss5566537193, ss5729582264, ss5809563066, ss5856310384, ss5888242926	NC_000008.11:26773219:C:T	NC_000008.11:26773219:C:T	(self)
ss14323557, ss19755897	NT_023666.16:5005021:C:T	NC_000008.11:26773219:C:T	(self)
ss1377254, ss5528596, ss5856188, ss43202513, ss65788364, ss74989763, ss86216385, ss105608069, ss119374505, ss143354089, ss156178346, ss161633597, ss174827493	NT_167187.1:14488882:C:T	NC_000008.11:26773219:C: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 rs937351

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

rs937351