Name: rs3761931
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.

rs3761931

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:113614401 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: A=0.205928 (54507/264690, TOPMED)
A=0.283324 (42600/150358, ALFA)
A=0.210175 (29411/139936, GnomAD) (+ 18 more)
A=0.07345 (1231/16760, 8.3KJPN)
A=0.1910 (1223/6404, 1000G_30x)
A=0.1939 (971/5008, 1000G)
A=0.2308 (1034/4480, Estonian)
A=0.2992 (1153/3854, ALSPAC)
A=0.2880 (1068/3708, TWINSUK)
A=0.0893 (261/2922, KOREAN)
A=0.1497 (280/1870, HapMap)
A=0.0655 (120/1832, Korea1K)
A=0.280 (279/998, GoNL)
A=0.217 (136/626, Chileans)
A=0.248 (149/600, NorthernSweden)
A=0.249 (133/534, MGP)
A=0.315 (68/216, Qatari)
A=0.201 (43/214, Vietnamese)
G=0.385 (77/200, SGDP_PRJ)
A=0.33 (13/40, GENOME_DK)
G=0.47 (14/30, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAGI3 : 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: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele
Total	Global	150358	G=0.716676	A=0.283324
European	Sub	126018	G=0.698146	A=0.301854
African	Sub	7342	G=0.9428	A=0.0572
African Others	Sub	254	G=0.996	A=0.004
African American	Sub	7088	G=0.9409	A=0.0591
Asian	Sub	676	G=0.891	A=0.109
East Asian	Sub	514	G=0.920	A=0.080
Other Asian	Sub	162	G=0.796	A=0.204
Latin American 1	Sub	888	G=0.787	A=0.213
Latin American 2	Sub	8374	G=0.7622	A=0.2378
South Asian	Sub	194	G=0.619	A=0.381
Other	Sub	6866	G=0.7359	A=0.2641

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	G=0.794072	A=0.205928
Allele Frequency Aggregator	Total	Global	150358	G=0.716676	A=0.283324
Allele Frequency Aggregator	European	Sub	126018	G=0.698146	A=0.301854
Allele Frequency Aggregator	Latin American 2	Sub	8374	G=0.7622	A=0.2378
Allele Frequency Aggregator	African	Sub	7342	G=0.9428	A=0.0572
Allele Frequency Aggregator	Other	Sub	6866	G=0.7359	A=0.2641
Allele Frequency Aggregator	Latin American 1	Sub	888	G=0.787	A=0.213
Allele Frequency Aggregator	Asian	Sub	676	G=0.891	A=0.109
Allele Frequency Aggregator	South Asian	Sub	194	G=0.619	A=0.381
gnomAD - Genomes	Global	Study-wide	139936	G=0.789825	A=0.210175
gnomAD - Genomes	European	Sub	75772	G=0.71109	A=0.28891
gnomAD - Genomes	African	Sub	41944	G=0.93944	A=0.06056
gnomAD - Genomes	American	Sub	13622	G=0.76817	A=0.23183
gnomAD - Genomes	Ashkenazi Jewish	Sub	3322	G=0.7011	A=0.2989
gnomAD - Genomes	East Asian	Sub	3130	G=0.8974	A=0.1026
gnomAD - Genomes	Other	Sub	2146	G=0.7633	A=0.2367
8.3KJPN	JAPANESE	Study-wide	16760	G=0.92655	A=0.07345
1000Genomes_30x	Global	Study-wide	6404	G=0.8090	A=0.1910
1000Genomes_30x	African	Sub	1786	G=0.9922	A=0.0078
1000Genomes_30x	Europe	Sub	1266	G=0.6761	A=0.3239
1000Genomes_30x	South Asian	Sub	1202	G=0.6007	A=0.3993
1000Genomes_30x	East Asian	Sub	1170	G=0.9043	A=0.0957
1000Genomes_30x	American	Sub	980	G=0.789	A=0.211
1000Genomes	Global	Study-wide	5008	G=0.8061	A=0.1939
1000Genomes	African	Sub	1322	G=0.9909	A=0.0091
1000Genomes	East Asian	Sub	1008	G=0.9058	A=0.0942
1000Genomes	Europe	Sub	1006	G=0.6740	A=0.3260
1000Genomes	South Asian	Sub	978	G=0.597	A=0.403
1000Genomes	American	Sub	694	G=0.795	A=0.205
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.7692	A=0.2308
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.7008	A=0.2992
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.7120	A=0.2880
KOREAN population from KRGDB	KOREAN	Study-wide	2922	G=0.9107	A=0.0893
HapMap	Global	Study-wide	1870	G=0.8503	A=0.1497
HapMap	American	Sub	762	G=0.764	A=0.236
HapMap	African	Sub	686	G=0.966	A=0.034
HapMap	Asian	Sub	248	G=0.923	A=0.077
HapMap	Europe	Sub	174	G=0.667	A=0.333
Korean Genome Project	KOREAN	Study-wide	1832	G=0.9345	A=0.0655
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.720	A=0.280
Chileans	Chilean	Study-wide	626	G=0.783	A=0.217
Northern Sweden	ACPOP	Study-wide	600	G=0.752	A=0.248
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.751	A=0.249
Qatari	Global	Study-wide	216	G=0.685	A=0.315
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.799	A=0.201
SGDP_PRJ	Global	Study-wide	200	G=0.385	A=0.615
The Danish reference pan genome	Danish	Study-wide	40	G=0.68	A=0.33
Siberian	Global	Study-wide	30	G=0.47	A=0.53

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.113614401G>A
GRCh38.p14 chr 1	NC_000001.11:g.113614401G>T
GRCh37.p13 chr 1	NC_000001.10:g.114157023G>A
GRCh37.p13 chr 1	NC_000001.10:g.114157023G>T

Gene: MAGI3, membrane associated guanylate kinase, WW and PDZ domain containing 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAGI3 transcript variant 1	NM_001142782.2:c.1019-200… NM_001142782.2:c.1019-200G>A	N/A	Intron Variant
MAGI3 transcript variant 2	NM_152900.3:c.1019-200G>A	N/A	Intron Variant
MAGI3 transcript variant X2	XM_005270737.4:c.1019-200… XM_005270737.4:c.1019-200G>A	N/A	Intron Variant
MAGI3 transcript variant X1	XM_017000974.2:c.1019-200… XM_017000974.2:c.1019-200G>A	N/A	Intron Variant
MAGI3 transcript variant X3	XM_047417371.1:c.1019-200… XM_047417371.1:c.1019-200G>A	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	G=	A	T
GRCh38.p14 chr 1	NC_000001.11:g.113614401=	NC_000001.11:g.113614401G>A	NC_000001.11:g.113614401G>T
GRCh37.p13 chr 1	NC_000001.10:g.114157023=	NC_000001.10:g.114157023G>A	NC_000001.10:g.114157023G>T
MAGI3 transcript variant 1	NM_001142782.1:c.1019-200=	NM_001142782.1:c.1019-200G>A	NM_001142782.1:c.1019-200G>T
MAGI3 transcript variant 1	NM_001142782.2:c.1019-200=	NM_001142782.2:c.1019-200G>A	NM_001142782.2:c.1019-200G>T
MAGI3 transcript variant 2	NM_152900.2:c.1019-200=	NM_152900.2:c.1019-200G>A	NM_152900.2:c.1019-200G>T
MAGI3 transcript variant 2	NM_152900.3:c.1019-200=	NM_152900.3:c.1019-200G>A	NM_152900.3:c.1019-200G>T
MAGI3 transcript variant X1	XM_005270736.1:c.1019-200=	XM_005270736.1:c.1019-200G>A	XM_005270736.1:c.1019-200G>T
MAGI3 transcript variant X2	XM_005270737.1:c.1019-200=	XM_005270737.1:c.1019-200G>A	XM_005270737.1:c.1019-200G>T
MAGI3 transcript variant X2	XM_005270737.4:c.1019-200=	XM_005270737.4:c.1019-200G>A	XM_005270737.4:c.1019-200G>T
MAGI3 transcript variant X1	XM_017000974.2:c.1019-200=	XM_017000974.2:c.1019-200G>A	XM_017000974.2:c.1019-200G>T
MAGI3 transcript variant X3	XM_047417371.1:c.1019-200=	XM_047417371.1:c.1019-200G>A	XM_047417371.1:c.1019-200G>T

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#.

108 SubSNP, 23 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4947966	Aug 28, 2002 (107)
2	PERLEGEN	ss24629854	Sep 20, 2004 (123)
3	ABI	ss43990049	Mar 15, 2006 (126)
4	ILLUMINA	ss65776803	Oct 14, 2006 (127)
5	AFFY	ss66162429	Nov 29, 2006 (127)
6	PERLEGEN	ss68778393	May 16, 2007 (127)
7	ILLUMINA	ss74898722	Dec 07, 2007 (129)
8	AFFY	ss76206632	Dec 08, 2007 (130)
9	KRIBB_YJKIM	ss81949009	Dec 15, 2007 (130)
10	BCMHGSC_JDW	ss87726799	Mar 23, 2008 (129)
11	HUMANGENOME_JCVI	ss99242207	Feb 06, 2009 (130)
12	BGI	ss106596085	Feb 06, 2009 (130)
13	1000GENOMES	ss108537040	Jan 23, 2009 (130)
14	ENSEMBL	ss138063307	Dec 01, 2009 (131)
15	ILLUMINA	ss160638125	Dec 01, 2009 (131)
16	COMPLETE_GENOMICS	ss165057837	Jul 04, 2010 (132)
17	COMPLETE_GENOMICS	ss167018300	Jul 04, 2010 (132)
18	AFFY	ss172810866	Jul 04, 2010 (132)
19	ILLUMINA	ss173628659	Jul 04, 2010 (132)
20	BUSHMAN	ss198954220	Jul 04, 2010 (132)
21	1000GENOMES	ss230698417	Jul 14, 2010 (132)
22	1000GENOMES	ss238354742	Jul 15, 2010 (132)
23	BL	ss253396548	May 09, 2011 (134)
24	GMI	ss275984441	May 04, 2012 (137)
25	PJP	ss290602161	May 09, 2011 (134)
26	ILLUMINA	ss480821465	May 04, 2012 (137)
27	ILLUMINA	ss480837149	May 04, 2012 (137)
28	ILLUMINA	ss481767279	Sep 08, 2015 (146)
29	ILLUMINA	ss485205550	May 04, 2012 (137)
30	ILLUMINA	ss537190350	Sep 08, 2015 (146)
31	TISHKOFF	ss554594217	Apr 25, 2013 (138)
32	SSMP	ss648323576	Apr 25, 2013 (138)
33	ILLUMINA	ss778522833	Sep 08, 2015 (146)
34	ILLUMINA	ss783048753	Sep 08, 2015 (146)
35	ILLUMINA	ss784007398	Sep 08, 2015 (146)
36	ILLUMINA	ss832306564	Sep 08, 2015 (146)
37	ILLUMINA	ss833979264	Sep 08, 2015 (146)
38	EVA-GONL	ss975587292	Aug 21, 2014 (142)
39	JMKIDD_LAB	ss1068205480	Aug 21, 2014 (142)
40	1000GENOMES	ss1292497320	Aug 21, 2014 (142)
41	DDI	ss1425942304	Apr 01, 2015 (144)
42	EVA_GENOME_DK	ss1574333833	Apr 01, 2015 (144)
43	EVA_DECODE	ss1584968148	Apr 01, 2015 (144)
44	EVA_UK10K_ALSPAC	ss1601024793	Apr 01, 2015 (144)
45	EVA_UK10K_TWINSUK	ss1644018826	Apr 01, 2015 (144)
46	EVA_MGP	ss1710916651	Apr 01, 2015 (144)
47	EVA_SVP	ss1712364381	Apr 01, 2015 (144)
48	ILLUMINA	ss1751864494	Sep 08, 2015 (146)
49	WEILL_CORNELL_DGM	ss1918787574	Feb 12, 2016 (147)
50	GENOMED	ss1966845318	Jul 19, 2016 (147)
51	JJLAB	ss2019918236	Sep 14, 2016 (149)
52	ILLUMINA	ss2094847045	Dec 20, 2016 (150)
53	ILLUMINA	ss2094972290	Dec 20, 2016 (150)
54	USC_VALOUEV	ss2147936958	Dec 20, 2016 (150)
55	HUMAN_LONGEVITY	ss2165847138	Dec 20, 2016 (150)
56	ILLUMINA	ss2632565349	Nov 08, 2017 (151)
57	GRF	ss2697867272	Nov 08, 2017 (151)
58	GNOMAD	ss2759745256	Nov 08, 2017 (151)
59	SWEGEN	ss2987465284	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3023723654	Nov 08, 2017 (151)
61	CSHL	ss3343642732	Nov 08, 2017 (151)
62	ILLUMINA	ss3626186653	Oct 11, 2018 (152)
63	ILLUMINA	ss3630598917	Oct 11, 2018 (152)
64	ILLUMINA	ss3632906750	Oct 11, 2018 (152)
65	ILLUMINA	ss3633601909	Oct 11, 2018 (152)
66	ILLUMINA	ss3634344016	Oct 11, 2018 (152)
67	ILLUMINA	ss3635295441	Oct 11, 2018 (152)
68	ILLUMINA	ss3636022130	Oct 11, 2018 (152)
69	ILLUMINA	ss3637045912	Oct 11, 2018 (152)
70	ILLUMINA	ss3637781092	Oct 11, 2018 (152)
71	ILLUMINA	ss3640051375	Oct 11, 2018 (152)
72	ILLUMINA	ss3640985374	Oct 11, 2018 (152)
73	ILLUMINA	ss3641279381	Oct 11, 2018 (152)
74	ILLUMINA	ss3642790781	Oct 11, 2018 (152)
75	URBANLAB	ss3646756283	Oct 11, 2018 (152)
76	ILLUMINA	ss3651455095	Oct 11, 2018 (152)
77	EGCUT_WGS	ss3655554234	Jul 12, 2019 (153)
78	EVA_DECODE	ss3687563027	Jul 12, 2019 (153)
79	ACPOP	ss3727402765	Jul 12, 2019 (153)
80	ILLUMINA	ss3744644964	Jul 12, 2019 (153)
81	EVA	ss3746692233	Jul 12, 2019 (153)
82	ILLUMINA	ss3772146159	Jul 12, 2019 (153)
83	KHV_HUMAN_GENOMES	ss3799695040	Jul 12, 2019 (153)
84	EVA	ss3826378531	Apr 25, 2020 (154)
85	EVA	ss3836580974	Apr 25, 2020 (154)
86	EVA	ss3841989414	Apr 25, 2020 (154)
87	SGDP_PRJ	ss3849683731	Apr 25, 2020 (154)
88	KRGDB	ss3894781843	Apr 25, 2020 (154)
89	KOGIC	ss3945280608	Apr 25, 2020 (154)
90	EVA	ss4016932882	Apr 25, 2021 (155)
91	TOPMED	ss4464175436	Apr 25, 2021 (155)
92	TOMMO_GENOMICS	ss5145754820	Apr 25, 2021 (155)
93	1000G_HIGH_COVERAGE	ss5243665813	Oct 12, 2022 (156)
94	EVA	ss5314645119	Oct 12, 2022 (156)
95	EVA	ss5321287163	Oct 12, 2022 (156)
96	HUGCELL_USP	ss5444583580	Oct 12, 2022 (156)
97	EVA	ss5506002522	Oct 12, 2022 (156)
98	1000G_HIGH_COVERAGE	ss5516687935	Oct 12, 2022 (156)
99	SANFORD_IMAGENETICS	ss5626330616	Oct 12, 2022 (156)
100	TOMMO_GENOMICS	ss5671045481	Oct 12, 2022 (156)
101	TOMMO_GENOMICS	ss5671045482	Oct 12, 2022 (156)
102	EVA	ss5799496398	Oct 12, 2022 (156)
103	YY_MCH	ss5800945885	Oct 12, 2022 (156)
104	EVA	ss5832505941	Oct 12, 2022 (156)
105	EVA	ss5849074521	Oct 12, 2022 (156)
106	EVA	ss5909865776	Oct 12, 2022 (156)
107	EVA	ss5938198182	Oct 12, 2022 (156)
108	EVA	ss5981195940	Oct 12, 2022 (156)
109	1000Genomes	NC_000001.10 - 114157023	Oct 11, 2018 (152)
110	1000Genomes_30x	NC_000001.11 - 113614401	Oct 12, 2022 (156)
111	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 114157023	Oct 11, 2018 (152)
112	Chileans	NC_000001.10 - 114157023	Apr 25, 2020 (154)
113	Genetic variation in the Estonian population	NC_000001.10 - 114157023	Oct 11, 2018 (152)
114	The Danish reference pan genome	NC_000001.10 - 114157023	Apr 25, 2020 (154)
115	gnomAD - Genomes	NC_000001.11 - 113614401	Apr 25, 2021 (155)
116	Genome of the Netherlands Release 5	NC_000001.10 - 114157023	Apr 25, 2020 (154)
117	HapMap	NC_000001.11 - 113614401	Apr 25, 2020 (154)
118	KOREAN population from KRGDB	NC_000001.10 - 114157023	Apr 25, 2020 (154)
119	Korean Genome Project	NC_000001.11 - 113614401	Apr 25, 2020 (154)
120	Medical Genome Project healthy controls from Spanish population	NC_000001.10 - 114157023	Apr 25, 2020 (154)
121	Northern Sweden	NC_000001.10 - 114157023	Jul 12, 2019 (153)
122	Qatari	NC_000001.10 - 114157023	Apr 25, 2020 (154)
123	SGDP_PRJ	NC_000001.10 - 114157023	Apr 25, 2020 (154)
124	Siberian	NC_000001.10 - 114157023	Apr 25, 2020 (154)
125	8.3KJPN	NC_000001.10 - 114157023	Apr 25, 2021 (155)
126	14KJPN Submission ignored due to conflicting rows: Row 4882585 (NC_000001.11:113614400:G:A 1998/28256) Row 4882586 (NC_000001.11:113614400:G:T 1/28256)	-	Oct 12, 2022 (156)
127	14KJPN Submission ignored due to conflicting rows: Row 4882585 (NC_000001.11:113614400:G:A 1998/28256) Row 4882586 (NC_000001.11:113614400:G:T 1/28256)	-	Oct 12, 2022 (156)
128	TopMed	NC_000001.11 - 113614401	Apr 25, 2021 (155)
129	UK 10K study - Twins	NC_000001.10 - 114157023	Oct 11, 2018 (152)
130	A Vietnamese Genetic Variation Database	NC_000001.10 - 114157023	Jul 12, 2019 (153)
131	ALFA	NC_000001.11 - 113614401	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)
rs17359247	Oct 07, 2004 (123)
rs56539826	May 25, 2008 (130)
rs59713164	Feb 27, 2009 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss87726799, ss108537040, ss165057837, ss167018300, ss198954220, ss253396548, ss275984441, ss290602161, ss480821465, ss1584968148, ss1712364381, ss2094847045, ss3642790781	NC_000001.9:113958545:G:A	NC_000001.11:113614400:G:A	(self)
3275530, 1812155, 18981, 1292482, 1671525, 788144, 1959237, 33403, 687630, 829504, 1700711, 453312, 3724127, 1812155, 392410, ss230698417, ss238354742, ss480837149, ss481767279, ss485205550, ss537190350, ss554594217, ss648323576, ss778522833, ss783048753, ss784007398, ss832306564, ss833979264, ss975587292, ss1068205480, ss1292497320, ss1425942304, ss1574333833, ss1601024793, ss1644018826, ss1710916651, ss1751864494, ss1918787574, ss1966845318, ss2019918236, ss2094972290, ss2147936958, ss2632565349, ss2697867272, ss2759745256, ss2987465284, ss3343642732, ss3626186653, ss3630598917, ss3632906750, ss3633601909, ss3634344016, ss3635295441, ss3636022130, ss3637045912, ss3637781092, ss3640051375, ss3640985374, ss3641279381, ss3651455095, ss3655554234, ss3727402765, ss3744644964, ss3746692233, ss3772146159, ss3826378531, ss3836580974, ss3849683731, ss3894781843, ss4016932882, ss5145754820, ss5314645119, ss5321287163, ss5506002522, ss5626330616, ss5799496398, ss5832505941, ss5938198182	NC_000001.10:114157022:G:A	NC_000001.11:113614400:G:A	(self)
4213870, 23165547, 158321, 1658609, 27781771, 3337411420, ss2165847138, ss3023723654, ss3646756283, ss3687563027, ss3799695040, ss3841989414, ss3945280608, ss4464175436, ss5243665813, ss5444583580, ss5516687935, ss5671045481, ss5800945885, ss5849074521, ss5909865776	NC_000001.11:113614400:G:A	NC_000001.11:113614400:G:A	(self)
ss4947966, ss24629854, ss43990049, ss65776803, ss66162429, ss68778393, ss74898722, ss76206632, ss81949009, ss99242207, ss106596085, ss138063307, ss160638125, ss172810866, ss173628659	NT_032977.9:84128940:G:A	NC_000001.11:113614400:G:A	(self)
ss5981195940	NC_000001.10:114157022:G:T	NC_000001.11:113614400:G:T
ss5671045482	NC_000001.11:113614400:G:T	NC_000001.11:113614400:G:T

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

No publications for rs3761931

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

rs3761931