Name: rs3094315
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.

rs3094315

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:817186 (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: G=0.195872 (35709/182308, ALFA)
G=0.298180 (41741/139986, GnomAD)
G=0.16257 (4594/28258, 14KJPN) (+ 19 more)
G=0.16205 (2716/16760, 8.3KJPN)
G=0.2937 (1881/6404, 1000G_30x)
G=0.2817 (1411/5008, 1000G)
G=0.1518 (585/3854, ALSPAC)
G=0.1580 (586/3708, TWINSUK)
G=0.1638 (480/2930, KOREAN)
G=0.2385 (496/2080, HGDP_Stanford)
G=0.1643 (301/1832, Korea1K)
G=0.3001 (428/1426, HapMap)
G=0.1642 (178/1084, Daghestan)
G=0.173 (173/998, GoNL)
G=0.104 (81/776, PRJEB37584)
G=0.148 (89/600, NorthernSweden)
G=0.169 (89/528, SGDP_PRJ)
G=0.259 (56/216, Qatari)
G=0.079 (17/216, Vietnamese)
G=0.15 (8/52, Ancient Sardinia)
G=0.15 (8/52, Siberian)
G=0.05 (2/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAM87B : 2KB Upstream Variant
Publications: 2 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	182308	G=0.195872	A=0.804128, T=0.000000
European	Sub	155548	G=0.178215	A=0.821785, T=0.000000
African	Sub	6318	G=0.5690	A=0.4310, T=0.0000
African Others	Sub	240	G=0.625	A=0.375, T=0.000
African American	Sub	6078	G=0.5668	A=0.4332, T=0.0000
Asian	Sub	452	G=0.095	A=0.905, T=0.000
East Asian	Sub	340	G=0.106	A=0.894, T=0.000
Other Asian	Sub	112	G=0.062	A=0.938, T=0.000
Latin American 1	Sub	808	G=0.254	A=0.746, T=0.000
Latin American 2	Sub	6724	G=0.2070	A=0.7930, T=0.0000
South Asian	Sub	5006	G=0.2099	A=0.7901, T=0.0000
Other	Sub	7452	G=0.2284	A=0.7716, T=0.0000

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
Allele Frequency Aggregator	Total	Global	182308	G=0.195872	A=0.804128, T=0.000000
Allele Frequency Aggregator	European	Sub	155548	G=0.178215	A=0.821785, T=0.000000
Allele Frequency Aggregator	Other	Sub	7452	G=0.2284	A=0.7716, T=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	6724	G=0.2070	A=0.7930, T=0.0000
Allele Frequency Aggregator	African	Sub	6318	G=0.5690	A=0.4310, T=0.0000
Allele Frequency Aggregator	South Asian	Sub	5006	G=0.2099	A=0.7901, T=0.0000
Allele Frequency Aggregator	Latin American 1	Sub	808	G=0.254	A=0.746, T=0.000
Allele Frequency Aggregator	Asian	Sub	452	G=0.095	A=0.905, T=0.000
gnomAD - Genomes	Global	Study-wide	139986	G=0.298180	A=0.701820
gnomAD - Genomes	European	Sub	75838	G=0.18015	A=0.81985
gnomAD - Genomes	African	Sub	41916	G=0.56243	A=0.43757
gnomAD - Genomes	American	Sub	13638	G=0.21374	A=0.78626
gnomAD - Genomes	Ashkenazi Jewish	Sub	3310	G=0.2157	A=0.7843
gnomAD - Genomes	East Asian	Sub	3134	G=0.1031	A=0.8969
gnomAD - Genomes	Other	Sub	2150	G=0.2567	A=0.7433
14KJPN	JAPANESE	Study-wide	28258	G=0.16257	A=0.83743
8.3KJPN	JAPANESE	Study-wide	16760	G=0.16205	A=0.83795
1000Genomes_30x	Global	Study-wide	6404	G=0.2937	A=0.7063
1000Genomes_30x	African	Sub	1786	G=0.6215	A=0.3785
1000Genomes_30x	Europe	Sub	1266	G=0.1580	A=0.8420
1000Genomes_30x	South Asian	Sub	1202	G=0.1980	A=0.8020
1000Genomes_30x	East Asian	Sub	1170	G=0.1179	A=0.8821
1000Genomes_30x	American	Sub	980	G=0.199	A=0.801
1000Genomes	Global	Study-wide	5008	G=0.2817	A=0.7183
1000Genomes	African	Sub	1322	G=0.6127	A=0.3873
1000Genomes	East Asian	Sub	1008	G=0.1161	A=0.8839
1000Genomes	Europe	Sub	1006	G=0.1600	A=0.8400
1000Genomes	South Asian	Sub	978	G=0.191	A=0.809
1000Genomes	American	Sub	694	G=0.196	A=0.804
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.1518	A=0.8482
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.1580	A=0.8420
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.1638	A=0.8362
HGDP-CEPH-db Supplement 1	Global	Study-wide	2080	G=0.2385	A=0.7615
HGDP-CEPH-db Supplement 1	Est_Asia	Sub	468	G=0.098	A=0.902
HGDP-CEPH-db Supplement 1	Central_South_Asia	Sub	412	G=0.238	A=0.762
HGDP-CEPH-db Supplement 1	Middle_Est	Sub	350	G=0.266	A=0.734
HGDP-CEPH-db Supplement 1	Europe	Sub	320	G=0.141	A=0.859
HGDP-CEPH-db Supplement 1	Africa	Sub	242	G=0.607	A=0.393
HGDP-CEPH-db Supplement 1	America	Sub	216	G=0.287	A=0.713
HGDP-CEPH-db Supplement 1	Oceania	Sub	72	G=0.07	A=0.93
Korean Genome Project	KOREAN	Study-wide	1832	G=0.1643	A=0.8357
HapMap	Global	Study-wide	1426	G=0.3001	A=0.6999
HapMap	American	Sub	592	G=0.211	A=0.789
HapMap	African	Sub	406	G=0.616	A=0.384
HapMap	Asian	Sub	252	G=0.111	A=0.889
HapMap	Europe	Sub	176	G=0.142	A=0.858
Genome-wide autozygosity in Daghestan	Global	Study-wide	1084	G=0.1642	A=0.8358
Genome-wide autozygosity in Daghestan	Daghestan	Sub	584	G=0.152	A=0.848
Genome-wide autozygosity in Daghestan	Near_East	Sub	138	G=0.196	A=0.804
Genome-wide autozygosity in Daghestan	Central Asia	Sub	122	G=0.115	A=0.885
Genome-wide autozygosity in Daghestan	Europe	Sub	106	G=0.198	A=0.802
Genome-wide autozygosity in Daghestan	South Asian	Sub	98	G=0.23	A=0.77
Genome-wide autozygosity in Daghestan	Caucasus	Sub	36	G=0.11	A=0.89
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.173	A=0.827
CNV burdens in cranial meningiomas	Global	Study-wide	776	G=0.104	A=0.896
CNV burdens in cranial meningiomas	CRM	Sub	776	G=0.104	A=0.896
Northern Sweden	ACPOP	Study-wide	600	G=0.148	A=0.852
SGDP_PRJ	Global	Study-wide	528	G=0.169	A=0.831
Qatari	Global	Study-wide	216	G=0.259	A=0.741
A Vietnamese Genetic Variation Database	Global	Study-wide	216	G=0.079	A=0.921
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	52	G=0.15	A=0.85
Siberian	Global	Study-wide	52	G=0.15	A=0.85
The Danish reference pan genome	Danish	Study-wide	40	G=0.05	A=0.95

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.817186G>A
GRCh38.p14 chr 1	NC_000001.11:g.817186G>T
GRCh37.p13 chr 1	NC_000001.10:g.752566G>A
GRCh37.p13 chr 1	NC_000001.10:g.752566G>T

Gene: FAM87B, family with sequence similarity 87 member B (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
FAM87B transcript	NR_103536.1:n.	N/A	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	G=	A	T
GRCh38.p14 chr 1	NC_000001.11:g.817186=	NC_000001.11:g.817186G>A	NC_000001.11:g.817186G>T
GRCh37.p13 chr 1	NC_000001.10:g.752566=	NC_000001.10:g.752566G>A	NC_000001.10:g.752566G>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#.

127 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SC_JCM	ss4329692	Mar 26, 2002 (103)
2	BCM_SSAHASNP	ss9839052	Jul 11, 2003 (116)
3	PERLEGEN	ss23686495	Sep 20, 2004 (124)
4	ILLUMINA	ss67289611	Dec 02, 2006 (127)
5	ILLUMINA	ss67692986	Dec 02, 2006 (127)
6	ILLUMINA	ss68217515	Dec 12, 2006 (127)
7	ILLUMINA	ss70768185	May 26, 2008 (130)
8	ILLUMINA	ss71343104	May 18, 2007 (127)
9	ILLUMINA	ss75526344	Dec 07, 2007 (129)
10	HGSV	ss78451817	Dec 07, 2007 (129)
11	KRIBB_YJKIM	ss84145714	Dec 16, 2007 (130)
12	BCMHGSC_JDW	ss87155625	Mar 23, 2008 (129)
13	HUMANGENOME_JCVI	ss97913181	Feb 06, 2009 (130)
14	BGI	ss105111644	Dec 01, 2009 (131)
15	1000GENOMES	ss107938262	Jan 22, 2009 (130)
16	1000GENOMES	ss109937159	Jan 24, 2009 (130)
17	ILLUMINA-UK	ss118438190	Dec 01, 2009 (131)
18	ENSEMBL	ss137752171	Dec 01, 2009 (131)
19	ENSEMBL	ss138899081	Dec 01, 2009 (131)
20	ILLUMINA	ss154253192	Dec 01, 2009 (131)
21	GMI	ss154522299	Dec 01, 2009 (131)
22	ILLUMINA	ss159430053	Dec 01, 2009 (131)
23	ILLUMINA	ss160609556	Dec 01, 2009 (131)
24	COMPLETE_GENOMICS	ss162980823	Jul 04, 2010 (132)
25	COMPLETE_GENOMICS	ss163702689	Jul 04, 2010 (132)
26	COMPLETE_GENOMICS	ss165981001	Jul 04, 2010 (132)
27	ILLUMINA	ss173559640	Jul 04, 2010 (132)
28	BUSHMAN	ss197885383	Jul 04, 2010 (132)
29	1000GENOMES	ss218190359	Jul 14, 2010 (132)
30	1000GENOMES	ss230395423	Jul 14, 2010 (132)
31	1000GENOMES	ss238114951	Jul 15, 2010 (132)
32	BL	ss252864063	May 09, 2011 (134)
33	GMI	ss275680742	May 04, 2012 (137)
34	GMI	ss283987352	Apr 25, 2013 (138)
35	PJP	ss290493764	May 09, 2011 (134)
36	ILLUMINA	ss480749373	May 04, 2012 (137)
37	ILLUMINA	ss480765278	May 04, 2012 (137)
38	ILLUMINA	ss481652678	Sep 08, 2015 (146)
39	ILLUMINA	ss485169458	May 04, 2012 (137)
40	ILLUMINA	ss537160571	Sep 08, 2015 (146)
41	TISHKOFF	ss553710350	Apr 25, 2013 (138)
42	SSMP	ss647516064	Apr 25, 2013 (138)
43	ILLUMINA	ss778515488	Sep 08, 2015 (146)
44	ILLUMINA	ss783030938	Sep 08, 2015 (146)
45	ILLUMINA	ss783990619	Sep 08, 2015 (146)
46	ILLUMINA	ss832288561	Sep 08, 2015 (146)
47	ILLUMINA	ss832941662	Jul 12, 2019 (153)
48	ILLUMINA	ss833971805	Sep 08, 2015 (146)
49	EVA-GONL	ss974769209	Aug 21, 2014 (142)
50	JMKIDD_LAB	ss1067612323	Aug 21, 2014 (142)
51	1000GENOMES	ss1289338797	Aug 21, 2014 (142)
52	HAMMER_LAB	ss1397238514	Sep 08, 2015 (146)
53	DDI	ss1425684785	Apr 01, 2015 (144)
54	EVA_GENOME_DK	ss1573851122	Apr 01, 2015 (144)
55	EVA_DECODE	ss1584129421	Apr 01, 2015 (144)
56	EVA_UK10K_ALSPAC	ss1599378261	Apr 01, 2015 (144)
57	EVA_UK10K_TWINSUK	ss1642372294	Apr 01, 2015 (144)
58	EVA_SVP	ss1712305454	Apr 01, 2015 (144)
59	ILLUMINA	ss1751932608	Sep 08, 2015 (146)
60	HAMMER_LAB	ss1793705629	Sep 08, 2015 (146)
61	WEILL_CORNELL_DGM	ss1917960116	Feb 12, 2016 (147)
62	ILLUMINA	ss1945981587	Feb 12, 2016 (147)
63	ILLUMINA	ss1958229937	Feb 12, 2016 (147)
64	GENOMED	ss1966667311	Jul 19, 2016 (147)
65	JJLAB	ss2019498331	Sep 14, 2016 (149)
66	ILLUMINA	ss2137543862	Oct 11, 2018 (152)
67	ILLUMINA	ss2137543864	Oct 11, 2018 (152)
68	ILLUMINA	ss2137543866	Oct 11, 2018 (152)
69	ILLUMINA	ss2137543867	Oct 11, 2018 (152)
70	ILLUMINA	ss2137543870	Oct 11, 2018 (152)
71	HGDP	ss2137544059	Apr 25, 2020 (154)
72	EVA	ss2137544098	Apr 25, 2021 (155)
73	EVA	ss2137544280	Oct 12, 2022 (156)
74	EVA	ss2137544300	Oct 12, 2022 (156)
75	USC_VALOUEV	ss2147484243	Dec 20, 2016 (150)
76	ILLUMINA	ss2632465440	Nov 08, 2017 (151)
77	GRF	ss2697374431	Nov 08, 2017 (151)
78	ILLUMINA	ss2710663538	Nov 08, 2017 (151)
79	GNOMAD	ss2750636437	Nov 08, 2017 (151)
80	SWEGEN	ss2986148517	Nov 08, 2017 (151)
81	BIOINF_KMB_FNS_UNIBA	ss3023513704	Nov 08, 2017 (151)
82	CSHL	ss3343272375	Nov 08, 2017 (151)
83	ILLUMINA	ss3625523485	Oct 11, 2018 (152)
84	ILLUMINA	ss3626006468	Oct 11, 2018 (152)
85	ILLUMINA	ss3630505566	Oct 11, 2018 (152)
86	ILLUMINA	ss3632878026	Oct 11, 2018 (152)
87	ILLUMINA	ss3633571432	Oct 11, 2018 (152)
88	ILLUMINA	ss3634301811	Oct 11, 2018 (152)
89	ILLUMINA	ss3635265638	Oct 11, 2018 (152)
90	ILLUMINA	ss3635978592	Oct 11, 2018 (152)
91	ILLUMINA	ss3637015976	Oct 11, 2018 (152)
92	ILLUMINA	ss3637732354	Oct 11, 2018 (152)
93	ILLUMINA	ss3640009177	Oct 11, 2018 (152)
94	ILLUMINA	ss3642746656	Oct 11, 2018 (152)
95	ILLUMINA	ss3644477459	Oct 11, 2018 (152)
96	URBANLAB	ss3646581171	Oct 11, 2018 (152)
97	EVA_DECODE	ss3685991925	Jul 12, 2019 (153)
98	ACPOP	ss3726716170	Jul 12, 2019 (153)
99	ILLUMINA	ss3744040761	Jul 12, 2019 (153)
100	ILLUMINA	ss3744602743	Jul 12, 2019 (153)
101	EVA	ss3745720825	Jul 12, 2019 (153)
102	ILLUMINA	ss3772104508	Jul 12, 2019 (153)
103	PACBIO	ss3783302090	Jul 12, 2019 (153)
104	PACBIO	ss3788979961	Jul 12, 2019 (153)
105	PACBIO	ss3793852498	Jul 12, 2019 (153)
106	KHV_HUMAN_GENOMES	ss3798743419	Jul 12, 2019 (153)
107	EVA	ss3825981414	Apr 25, 2020 (154)
108	EVA	ss3836378355	Apr 25, 2020 (154)
109	EVA	ss3841782357	Apr 25, 2020 (154)
110	SGDP_PRJ	ss3847994707	Apr 25, 2020 (154)
111	KRGDB	ss3892835081	Apr 25, 2020 (154)
112	KOGIC	ss3943629077	Apr 25, 2020 (154)
113	EVA	ss3984450704	Apr 25, 2021 (155)
114	TOMMO_GENOMICS	ss5142050932	Apr 25, 2021 (155)
115	1000G_HIGH_COVERAGE	ss5240862477	Oct 12, 2022 (156)
116	EVA	ss5316182131	Oct 12, 2022 (156)
117	HUGCELL_USP	ss5442112007	Oct 12, 2022 (156)
118	1000G_HIGH_COVERAGE	ss5512487015	Oct 12, 2022 (156)
119	SANFORD_IMAGENETICS	ss5624748648	Oct 12, 2022 (156)
120	TOMMO_GENOMICS	ss5666189778	Oct 12, 2022 (156)
121	YY_MCH	ss5800243525	Oct 12, 2022 (156)
122	EVA	ss5831418010	Oct 12, 2022 (156)
123	EVA	ss5848748829	Oct 12, 2022 (156)
124	EVA	ss5906704345	Oct 12, 2022 (156)
125	EVA	ss5936582361	Oct 12, 2022 (156)
126	EVA	ss5979259171	Oct 12, 2022 (156)
127	EVA	ss5979925985	Oct 12, 2022 (156)
128	1000Genomes	NC_000001.10 - 752566	Oct 11, 2018 (152)
129	1000Genomes_30x	NC_000001.11 - 817186	Oct 12, 2022 (156)
130	The Avon Longitudinal Study of Parents and Children	NC_000001.10 - 752566	Oct 11, 2018 (152)
131	Genome-wide autozygosity in Daghestan	NC_000001.9 - 742429	Apr 25, 2020 (154)
132	The Danish reference pan genome	NC_000001.10 - 752566	Apr 25, 2020 (154)
133	gnomAD - Genomes	NC_000001.11 - 817186	Apr 25, 2021 (155)
134	Genome of the Netherlands Release 5	NC_000001.10 - 752566	Apr 25, 2020 (154)
135	HGDP-CEPH-db Supplement 1	NC_000001.9 - 742429	Apr 25, 2020 (154)
136	HapMap	NC_000001.11 - 817186	Apr 25, 2020 (154)
137	KOREAN population from KRGDB	NC_000001.10 - 752566	Apr 25, 2020 (154)
138	Korean Genome Project	NC_000001.11 - 817186	Apr 25, 2020 (154)
139	Northern Sweden	NC_000001.10 - 752566	Jul 12, 2019 (153)
140	Ancient Sardinia genome-wide 1240k capture data generation and analysis	NC_000001.10 - 752566	Apr 25, 2021 (155)
141	CNV burdens in cranial meningiomas	NC_000001.10 - 752566	Apr 25, 2021 (155)
142	Qatari	NC_000001.10 - 752566	Apr 25, 2020 (154)
143	SGDP_PRJ	NC_000001.10 - 752566	Apr 25, 2020 (154)
144	Siberian	NC_000001.10 - 752566	Apr 25, 2020 (154)
145	8.3KJPN	NC_000001.10 - 752566	Apr 25, 2021 (155)
146	14KJPN	NC_000001.11 - 817186	Oct 12, 2022 (156)
147	UK 10K study - Twins	NC_000001.10 - 752566	Oct 11, 2018 (152)
148	A Vietnamese Genetic Variation Database	NC_000001.10 - 752566	Jul 12, 2019 (153)
149	ALFA	NC_000001.11 - 817186	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)
rs17421318	Dec 02, 2004 (124)
rs56475322	May 26, 2008 (130)
rs61126360	May 26, 2008 (130)
rs112180858	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss78451817, ss2137543862, ss2137543864, ss2137543870	NC_000001.8:792428:G:A	NC_000001.11:817185:G:A	(self)
1, 1, ss87155625, ss107938262, ss109937159, ss118438190, ss162980823, ss163702689, ss165981001, ss197885383, ss252864063, ss275680742, ss283987352, ss290493764, ss480749373, ss1397238514, ss1584129421, ss1712305454, ss2137544059, ss3642746656	NC_000001.9:742428:G:A	NC_000001.11:817185:G:A	(self)
3509, 147, 1358356, 287, 12475, 1035, 1, 3, 2046, 11687, 597, 20239, 147, 32, ss218190359, ss230395423, ss238114951, ss480765278, ss481652678, ss485169458, ss537160571, ss553710350, ss647516064, ss778515488, ss783030938, ss783990619, ss832288561, ss832941662, ss833971805, ss974769209, ss1067612323, ss1289338797, ss1425684785, ss1573851122, ss1599378261, ss1642372294, ss1751932608, ss1793705629, ss1917960116, ss1945981587, ss1958229937, ss1966667311, ss2019498331, ss2137543866, ss2137543867, ss2137544098, ss2137544280, ss2137544300, ss2147484243, ss2632465440, ss2697374431, ss2710663538, ss2750636437, ss2986148517, ss3343272375, ss3625523485, ss3626006468, ss3630505566, ss3632878026, ss3633571432, ss3634301811, ss3635265638, ss3635978592, ss3637015976, ss3637732354, ss3640009177, ss3644477459, ss3726716170, ss3744040761, ss3744602743, ss3745720825, ss3772104508, ss3783302090, ss3788979961, ss3793852498, ss3825981414, ss3836378355, ss3847994707, ss3892835081, ss3984450704, ss5142050932, ss5316182131, ss5624748648, ss5831418010, ss5936582361, ss5979259171, ss5979925985	NC_000001.10:752565:G:A	NC_000001.11:817185:G:A	(self)
12950, 60679, 40, 7078, 26882, 3644886641, ss3023513704, ss3646581171, ss3685991925, ss3798743419, ss3841782357, ss3943629077, ss5240862477, ss5442112007, ss5512487015, ss5666189778, ss5800243525, ss5848748829, ss5906704345	NC_000001.11:817185:G:A	NC_000001.11:817185:G:A	(self)
ss4329692, ss23686495, ss67289611, ss67692986, ss68217515, ss70768185, ss71343104, ss75526344, ss84145714, ss97913181, ss105111644, ss137752171, ss138899081, ss154253192, ss154522299, ss159430053, ss160609556, ss173559640	NT_004350.19:231197:G:A	NC_000001.11:817185:G:A	(self)
ss9839052	NT_034471.3:231197:G:A	NC_000001.11:817185:G:A	(self)
3644886641	NC_000001.11:817185:G:T	NC_000001.11:817185:G:T	(self)

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

2 citations for rs3094315

PMID	Title	Author	Year	Journal
21159730	Damming the genomic data flood using a comprehensive analysis and storage data structure.	Bouffard M et al.	2010	Database
21492446	A Monte Carlo test of linkage disequilibrium for single nucleotide polymorphisms.	Xu H et al.	2011	BMC research notes

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

rs3094315