Name: rs3805251
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.

rs3805251

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:143374799 (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>T
Variation Type: SNV Single Nucleotide Variation
Frequency: C=0.485564 (128524/264690, TOPMED)
C=0.489653 (68524/139944, GnomAD)
T=0.472698 (51941/109882, ALFA) (+ 19 more)
T=0.25550 (7220/28258, 14KJPN)
T=0.25537 (4280/16760, 8.3KJPN)
C=0.4809 (3080/6404, 1000G_30x)
C=0.4820 (2414/5008, 1000G)
T=0.4580 (2052/4480, Estonian)
T=0.4359 (1680/3854, ALSPAC)
T=0.4523 (1677/3708, TWINSUK)
T=0.2328 (682/2930, KOREAN)
T=0.4909 (1023/2084, HGDP_Stanford)
T=0.4867 (913/1876, HapMap)
T=0.2495 (457/1832, Korea1K)
T=0.458 (457/998, GoNL)
T=0.442 (265/600, NorthernSweden)
C=0.347 (141/406, SGDP_PRJ)
T=0.440 (95/216, Qatari)
T=0.273 (59/216, Vietnamese)
T=0.42 (22/52, Ancient Sardinia)
T=0.30 (12/40, GENOME_DK)
C=0.35 (12/34, Siberian)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: GAB1 : 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	109882	C=0.527302	T=0.472698
European	Sub	90532	C=0.54876	T=0.45124
African	Sub	6710	C=0.3280	T=0.6720
African Others	Sub	246	C=0.317	T=0.683
African American	Sub	6464	C=0.3284	T=0.6716
Asian	Sub	530	C=0.738	T=0.262
East Asian	Sub	450	C=0.747	T=0.253
Other Asian	Sub	80	C=0.69	T=0.31
Latin American 1	Sub	636	C=0.502	T=0.498
Latin American 2	Sub	1554	C=0.5476	T=0.4524
South Asian	Sub	5032	C=0.3712	T=0.6288
Other	Sub	4888	C=0.5383	T=0.4617

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=0.485564	T=0.514436
gnomAD - Genomes	Global	Study-wide	139944	C=0.489653	T=0.510347
gnomAD - Genomes	European	Sub	75790	C=0.55435	T=0.44565
gnomAD - Genomes	African	Sub	41926	C=0.33082	T=0.66918
gnomAD - Genomes	American	Sub	13636	C=0.55977	T=0.44023
gnomAD - Genomes	Ashkenazi Jewish	Sub	3320	C=0.5084	T=0.4916
gnomAD - Genomes	East Asian	Sub	3122	C=0.7252	T=0.2748
gnomAD - Genomes	Other	Sub	2150	C=0.4907	T=0.5093
Allele Frequency Aggregator	Total	Global	109882	C=0.527302	T=0.472698
Allele Frequency Aggregator	European	Sub	90532	C=0.54876	T=0.45124
Allele Frequency Aggregator	African	Sub	6710	C=0.3280	T=0.6720
Allele Frequency Aggregator	South Asian	Sub	5032	C=0.3712	T=0.6288
Allele Frequency Aggregator	Other	Sub	4888	C=0.5383	T=0.4617
Allele Frequency Aggregator	Latin American 2	Sub	1554	C=0.5476	T=0.4524
Allele Frequency Aggregator	Latin American 1	Sub	636	C=0.502	T=0.498
Allele Frequency Aggregator	Asian	Sub	530	C=0.738	T=0.262
14KJPN	JAPANESE	Study-wide	28258	C=0.74450	T=0.25550
8.3KJPN	JAPANESE	Study-wide	16760	C=0.74463	T=0.25537
1000Genomes_30x	Global	Study-wide	6404	C=0.4809	T=0.5191
1000Genomes_30x	African	Sub	1786	C=0.2732	T=0.7268
1000Genomes_30x	Europe	Sub	1266	C=0.5885	T=0.4115
1000Genomes_30x	South Asian	Sub	1202	C=0.3752	T=0.6248
1000Genomes_30x	East Asian	Sub	1170	C=0.7248	T=0.2752
1000Genomes_30x	American	Sub	980	C=0.559	T=0.441
1000Genomes	Global	Study-wide	5008	C=0.4820	T=0.5180
1000Genomes	African	Sub	1322	C=0.2761	T=0.7239
1000Genomes	East Asian	Sub	1008	C=0.7173	T=0.2827
1000Genomes	Europe	Sub	1006	C=0.5855	T=0.4145
1000Genomes	South Asian	Sub	978	C=0.358	T=0.642
1000Genomes	American	Sub	694	C=0.558	T=0.442
Genetic variation in the Estonian population	Estonian	Study-wide	4480	C=0.5420	T=0.4580
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.5641	T=0.4359
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.5477	T=0.4523
KOREAN population from KRGDB	KOREAN	Study-wide	2930	C=0.7672	T=0.2328
HGDP-CEPH-db Supplement 1	Global	Study-wide	2084	C=0.5091	T=0.4909
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	470	C=0.681	T=0.319
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	414	C=0.435	T=0.565
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	C=0.491	T=0.509
HGDP-CEPH-db Supplement 1	Europe	Sub	320	C=0.509	T=0.491
HGDP-CEPH-db Supplement 1	Africa	Sub	242	C=0.298	T=0.702
HGDP-CEPH-db Supplement 1	America	Sub	216	C=0.523	T=0.477
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	C=0.57	T=0.43
HapMap	Global	Study-wide	1876	C=0.5133	T=0.4867
HapMap	American	Sub	764	C=0.539	T=0.461
HapMap	African	Sub	688	C=0.391	T=0.609
HapMap	Asian	Sub	248	C=0.754	T=0.246
HapMap	Europe	Sub	176	C=0.540	T=0.460
Korean Genome Project	KOREAN	Study-wide	1832	C=0.7505	T=0.2495
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	C=0.542	T=0.458
Northern Sweden	ACPOP	Study-wide	600	C=0.558	T=0.442
SGDP_PRJ	Global	Study-wide	406	C=0.347	T=0.653
Qatari	Global	Study-wide	216	C=0.560	T=0.440
A Vietnamese Genetic Variation Database	Global	Study-wide	216	C=0.727	T=0.273
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	C=0.58	T=0.42
The Danish reference pan genome	Danish	Study-wide	40	C=0.70	T=0.30
Siberian	Global	Study-wide	34	C=0.35	T=0.65

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 4	NC_000004.12:g.143374799C>T
GRCh37.p13 chr 4	NC_000004.11:g.144295952C>T

Gene: GAB1, GRB2 associated binding protein 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
GAB1 transcript variant 2	NM_002039.4:c.72+37539C>T	N/A	Intron Variant
GAB1 transcript variant 1	NM_207123.3:c.72+37539C>T	N/A	Intron Variant
GAB1 transcript variant X9	XM_017007969.2:c.-238+296… XM_017007969.2:c.-238+29664C>T	N/A	Intron Variant
GAB1 transcript variant X10	XM_017007970.2:c.-238+206… XM_017007970.2:c.-238+20611C>T	N/A	Intron Variant
GAB1 transcript variant X3	XM_047449969.1:c.-4248-16… XM_047449969.1:c.-4248-16645C>T	N/A	Intron Variant
GAB1 transcript variant X1	XM_017007966.2:c.-18162=	N/A	5 Prime UTR Variant
GAB1 transcript variant X7	XM_006714168.5:c.-6178=	N/A	5 Prime UTR Variant
GAB1 transcript variant X12	XM_047449972.1:c.-6178=	N/A	5 Prime UTR Variant
GAB1 transcript variant X13	XM_047449973.1:c.-6178=	N/A	5 Prime UTR Variant
GAB1 transcript variant X14	XM_047449974.1:c.-6178=	N/A	5 Prime UTR Variant
GAB1 transcript variant X11	XM_006714167.5:c.	N/A	Genic Upstream Transcript Variant
GAB1 transcript variant X4	XM_017007967.2:c.	N/A	Genic Upstream Transcript Variant
GAB1 transcript variant X5	XM_017007968.2:c.	N/A	Genic Upstream Transcript Variant
GAB1 transcript variant X2	XM_047449968.1:c.	N/A	Genic Upstream Transcript Variant
GAB1 transcript variant X6	XM_047449970.1:c.	N/A	Genic Upstream Transcript Variant
GAB1 transcript variant X8	XM_047449971.1:c.	N/A	Genic Upstream 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=	T
GRCh38.p14 chr 4	NC_000004.12:g.143374799=	NC_000004.12:g.143374799C>T
GRCh37.p13 chr 4	NC_000004.11:g.144295952=	NC_000004.11:g.144295952C>T
GAB1 transcript variant X7	XM_006714168.5:c.-6178=	XM_006714168.5:c.-6178C>T
GAB1 transcript variant X1	XM_017007966.2:c.-18162=	XM_017007966.2:c.-18162C>T
GAB1 transcript variant X12	XM_047449972.1:c.-6178=	XM_047449972.1:c.-6178C>T
GAB1 transcript variant X13	XM_047449973.1:c.-6178=	XM_047449973.1:c.-6178C>T
GAB1 transcript variant X14	XM_047449974.1:c.-6178=	XM_047449974.1:c.-6178C>T
GAB1 transcript variant 2	NM_002039.3:c.72+37539=	NM_002039.3:c.72+37539C>T
GAB1 transcript variant 2	NM_002039.4:c.72+37539=	NM_002039.4:c.72+37539C>T
GAB1 transcript variant 1	NM_207123.2:c.72+37539=	NM_207123.2:c.72+37539C>T
GAB1 transcript variant 1	NM_207123.3:c.72+37539=	NM_207123.3:c.72+37539C>T
GAB1 transcript variant X1	XM_005262881.1:c.72+37539=	XM_005262881.1:c.72+37539C>T
GAB1 transcript variant X2	XM_005262882.1:c.72+37539=	XM_005262882.1:c.72+37539C>T
GAB1 transcript variant X9	XM_017007969.2:c.-238+29664=	XM_017007969.2:c.-238+29664C>T
GAB1 transcript variant X10	XM_017007970.2:c.-238+20611=	XM_017007970.2:c.-238+20611C>T
GAB1 transcript variant X3	XM_047449969.1:c.-4248-16645=	XM_047449969.1:c.-4248-16645C>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#.

102 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4991641	Aug 28, 2002 (107)
2	ILLUMINA	ss67304952	Dec 01, 2006 (127)
3	ILLUMINA	ss67710054	Dec 01, 2006 (127)
4	ILLUMINA	ss68222205	Dec 12, 2006 (127)
5	ILLUMINA	ss70783603	May 25, 2008 (130)
6	ILLUMINA	ss71360242	May 18, 2007 (127)
7	ILLUMINA	ss75908930	Dec 07, 2007 (129)
8	HGSV	ss82118514	Dec 15, 2007 (130)
9	KRIBB_YJKIM	ss84191620	Dec 15, 2007 (130)
10	BCMHGSC_JDW	ss92811874	Mar 24, 2008 (129)
11	1000GENOMES	ss108419936	Jan 23, 2009 (130)
12	1000GENOMES	ss110733367	Jan 25, 2009 (130)
13	ILLUMINA-UK	ss117221459	Feb 14, 2009 (130)
14	ENSEMBL	ss139934553	Dec 01, 2009 (131)
15	ILLUMINA	ss154271233	Dec 01, 2009 (131)
16	ILLUMINA	ss159447966	Dec 01, 2009 (131)
17	ILLUMINA	ss160644728	Dec 01, 2009 (131)
18	COMPLETE_GENOMICS	ss164598258	Jul 04, 2010 (132)
19	COMPLETE_GENOMICS	ss167254611	Jul 04, 2010 (132)
20	ILLUMINA	ss173646755	Jul 04, 2010 (132)
21	BUSHMAN	ss199291487	Jul 04, 2010 (132)
22	BCM-HGSC-SUB	ss206354294	Jul 04, 2010 (132)
23	1000GENOMES	ss221265225	Jul 14, 2010 (132)
24	1000GENOMES	ss232637733	Jul 14, 2010 (132)
25	1000GENOMES	ss239876469	Jul 15, 2010 (132)
26	BL	ss253589152	May 09, 2011 (134)
27	GMI	ss277971256	May 04, 2012 (137)
28	GMI	ss285023522	Apr 25, 2013 (138)
29	PJP	ss293207398	May 09, 2011 (134)
30	ILLUMINA	ss481793575	Sep 08, 2015 (146)
31	ILLUMINA	ss483196936	May 04, 2012 (137)
32	ILLUMINA	ss484714260	May 04, 2012 (137)
33	ILLUMINA	ss535417046	Sep 08, 2015 (146)
34	TISHKOFF	ss557915694	Apr 25, 2013 (138)
35	SSMP	ss651733943	Apr 25, 2013 (138)
36	ILLUMINA	ss779406678	Sep 08, 2015 (146)
37	ILLUMINA	ss782041750	Sep 08, 2015 (146)
38	ILLUMINA	ss832959523	Jul 13, 2019 (153)
39	ILLUMINA	ss834875660	Sep 08, 2015 (146)
40	EVA-GONL	ss980780647	Aug 21, 2014 (142)
41	JMKIDD_LAB	ss1072035038	Aug 21, 2014 (142)
42	1000GENOMES	ss1312196475	Aug 21, 2014 (142)
43	DDI	ss1430081625	Apr 01, 2015 (144)
44	EVA_GENOME_DK	ss1580818327	Apr 01, 2015 (144)
45	EVA_DECODE	ss1590293490	Apr 01, 2015 (144)
46	EVA_UK10K_ALSPAC	ss1611373371	Apr 01, 2015 (144)
47	EVA_UK10K_TWINSUK	ss1654367404	Apr 01, 2015 (144)
48	EVA_SVP	ss1712712820	Apr 01, 2015 (144)
49	HAMMER_LAB	ss1802334184	Sep 08, 2015 (146)
50	WEILL_CORNELL_DGM	ss1924022026	Feb 12, 2016 (147)
51	GENOMED	ss1969895240	Jul 19, 2016 (147)
52	JJLAB	ss2022598435	Sep 14, 2016 (149)
53	USC_VALOUEV	ss2150729984	Dec 20, 2016 (150)
54	HUMAN_LONGEVITY	ss2267936628	Dec 20, 2016 (150)
55	SYSTEMSBIOZJU	ss2625795569	Nov 08, 2017 (151)
56	ILLUMINA	ss2634188571	Nov 08, 2017 (151)
57	GRF	ss2706222498	Nov 08, 2017 (151)
58	GNOMAD	ss2816353122	Nov 08, 2017 (151)
59	SWEGEN	ss2995711993	Nov 08, 2017 (151)
60	BIOINF_KMB_FNS_UNIBA	ss3025076737	Nov 08, 2017 (151)
61	CSHL	ss3346007559	Nov 08, 2017 (151)
62	ILLUMINA	ss3629083925	Oct 12, 2018 (152)
63	ILLUMINA	ss3632120727	Oct 12, 2018 (152)
64	ILLUMINA	ss3636680882	Oct 12, 2018 (152)
65	ILLUMINA	ss3638516239	Oct 12, 2018 (152)
66	ILLUMINA	ss3639260378	Oct 12, 2018 (152)
67	ILLUMINA	ss3639928453	Oct 12, 2018 (152)
68	ILLUMINA	ss3643465333	Oct 12, 2018 (152)
69	ILLUMINA	ss3643974411	Oct 12, 2018 (152)
70	URBANLAB	ss3647872009	Oct 12, 2018 (152)
71	EGCUT_WGS	ss3663621674	Jul 13, 2019 (153)
72	EVA_DECODE	ss3713247373	Jul 13, 2019 (153)
73	ACPOP	ss3731693588	Jul 13, 2019 (153)
74	EVA	ss3762528415	Jul 13, 2019 (153)
75	PACBIO	ss3784889651	Jul 13, 2019 (153)
76	PACBIO	ss3790322037	Jul 13, 2019 (153)
77	PACBIO	ss3795197585	Jul 13, 2019 (153)
78	KHV_HUMAN_GENOMES	ss3805689980	Jul 13, 2019 (153)
79	EVA	ss3828859118	Apr 26, 2020 (154)
80	EVA	ss3837879065	Apr 26, 2020 (154)
81	EVA	ss3843318995	Apr 26, 2020 (154)
82	HGDP	ss3847767589	Apr 26, 2020 (154)
83	SGDP_PRJ	ss3860258401	Apr 26, 2020 (154)
84	KRGDB	ss3906590190	Apr 26, 2020 (154)
85	KOGIC	ss3955300589	Apr 26, 2020 (154)
86	EVA	ss3985100406	Apr 26, 2021 (155)
87	EVA	ss4017172767	Apr 26, 2021 (155)
88	TOPMED	ss4635338043	Apr 26, 2021 (155)
89	TOMMO_GENOMICS	ss5168436298	Apr 26, 2021 (155)
90	1000G_HIGH_COVERAGE	ss5261356500	Oct 17, 2022 (156)
91	EVA	ss5314997049	Oct 17, 2022 (156)
92	EVA	ss5352907003	Oct 17, 2022 (156)
93	HUGCELL_USP	ss5459880337	Oct 17, 2022 (156)
94	EVA	ss5507768362	Oct 17, 2022 (156)
95	1000G_HIGH_COVERAGE	ss5543628880	Oct 17, 2022 (156)
96	SANFORD_IMAGENETICS	ss5636291335	Oct 17, 2022 (156)
97	TOMMO_GENOMICS	ss5703546743	Oct 17, 2022 (156)
98	YY_MCH	ss5805621827	Oct 17, 2022 (156)
99	EVA	ss5844845334	Oct 17, 2022 (156)
100	EVA	ss5854486973	Oct 17, 2022 (156)
101	EVA	ss5865886111	Oct 17, 2022 (156)
102	EVA	ss5964695536	Oct 17, 2022 (156)
103	1000Genomes	NC_000004.11 - 144295952	Oct 12, 2018 (152)
104	1000Genomes_30x	NC_000004.12 - 143374799	Oct 17, 2022 (156)
105	The Avon Longitudinal Study of Parents and Children	NC_000004.11 - 144295952	Oct 12, 2018 (152)
106	Genetic variation in the Estonian population	NC_000004.11 - 144295952	Oct 12, 2018 (152)
107	The Danish reference pan genome	NC_000004.11 - 144295952	Apr 26, 2020 (154)
108	gnomAD - Genomes	NC_000004.12 - 143374799	Apr 26, 2021 (155)
109	Genome of the Netherlands Release 5	NC_000004.11 - 144295952	Apr 26, 2020 (154)
110	HGDP-CEPH-db Supplement 1	NC_000004.10 - 144515402	Apr 26, 2020 (154)
111	HapMap	NC_000004.12 - 143374799	Apr 26, 2020 (154)
112	KOREAN population from KRGDB	NC_000004.11 - 144295952	Apr 26, 2020 (154)
113	Korean Genome Project	NC_000004.12 - 143374799	Apr 26, 2020 (154)
114	Northern Sweden	NC_000004.11 - 144295952	Jul 13, 2019 (153)
115	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000004.11 - 144295952	Apr 26, 2021 (155)
116	Qatari	NC_000004.11 - 144295952	Apr 26, 2020 (154)
117	SGDP_PRJ	NC_000004.11 - 144295952	Apr 26, 2020 (154)
118	Siberian	NC_000004.11 - 144295952	Apr 26, 2020 (154)
119	8.3KJPN	NC_000004.11 - 144295952	Apr 26, 2021 (155)
120	14KJPN	NC_000004.12 - 143374799	Oct 17, 2022 (156)
121	TopMed	NC_000004.12 - 143374799	Apr 26, 2021 (155)
122	UK 10K study - Twins	NC_000004.11 - 144295952	Oct 12, 2018 (152)
123	A Vietnamese Genetic Variation Database	NC_000004.11 - 144295952	Jul 13, 2019 (153)
124	ALFA	NC_000004.12 - 143374799	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)
rs59135283	May 25, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss82118514, ss3639260378, ss3639928453, ss3643974411	NC_000004.9:144653556:C:T	NC_000004.12:143374798:C:T	(self)
445481, ss92811874, ss108419936, ss110733367, ss117221459, ss164598258, ss167254611, ss199291487, ss206354294, ss253589152, ss277971256, ss285023522, ss293207398, ss484714260, ss1590293490, ss1712712820, ss3643465333, ss3847767589	NC_000004.10:144515401:C:T	NC_000004.12:143374798:C:T	(self)
23686536, 13173102, 9359922, 6983266, 5835945, 13767584, 4978453, 326333, 6063956, 12275381, 3246338, 26405605, 13173102, 2907159, ss221265225, ss232637733, ss239876469, ss481793575, ss483196936, ss535417046, ss557915694, ss651733943, ss779406678, ss782041750, ss832959523, ss834875660, ss980780647, ss1072035038, ss1312196475, ss1430081625, ss1580818327, ss1611373371, ss1654367404, ss1802334184, ss1924022026, ss1969895240, ss2022598435, ss2150729984, ss2625795569, ss2634188571, ss2706222498, ss2816353122, ss2995711993, ss3346007559, ss3629083925, ss3632120727, ss3636680882, ss3638516239, ss3663621674, ss3731693588, ss3762528415, ss3784889651, ss3790322037, ss3795197585, ss3828859118, ss3837879065, ss3860258401, ss3906590190, ss3985100406, ss4017172767, ss5168436298, ss5314997049, ss5352907003, ss5507768362, ss5636291335, ss5844845334, ss5964695536	NC_000004.11:144295951:C:T	NC_000004.12:143374798:C:T	(self)
31154815, 167777304, 2726780, 11678590, 37383847, 472715599, 4189545502, ss2267936628, ss3025076737, ss3647872009, ss3713247373, ss3805689980, ss3843318995, ss3955300589, ss4635338043, ss5261356500, ss5459880337, ss5543628880, ss5703546743, ss5805621827, ss5854486973, ss5865886111	NC_000004.12:143374798:C:T	NC_000004.12:143374798:C:T	(self)
ss4991641, ss67304952, ss67710054, ss68222205, ss70783603, ss71360242, ss75908930, ss84191620, ss139934553, ss154271233, ss159447966, ss160644728, ss173646755	NT_016354.19:68843672:C:T	NC_000004.12:143374798: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 rs3805251

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

rs3805251