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dbSNP Short Genetic Variations

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 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:817186 (GRCh38.p13) 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=0.16205 (2716/16760, 8.3KJPN) (+ 17 more)
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
Help

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.p13 chr 1 NC_000001.11:g.817186G>A
GRCh38.p13 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
Help

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

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: 20201027095038
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


Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
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
8.3KJPN JAPANESE Study-wide 16760 G=0.16205 A=0.83795
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
Help

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.p13 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
Help

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#.

115 SubSNP, 20 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 USC_VALOUEV ss2147484243 Dec 20, 2016 (150)
74 TOPMED ss2321502621 Dec 20, 2016 (150)
75 ILLUMINA ss2632465440 Nov 08, 2017 (151)
76 GRF ss2697374431 Nov 08, 2017 (151)
77 ILLUMINA ss2710663538 Nov 08, 2017 (151)
78 GNOMAD ss2750636437 Nov 08, 2017 (151)
79 SWEGEN ss2986148517 Nov 08, 2017 (151)
80 BIOINF_KMB_FNS_UNIBA ss3023513704 Nov 08, 2017 (151)
81 TOPMED ss3066395614 Nov 08, 2017 (151)
82 TOPMED ss3066395615 Nov 08, 2017 (151)
83 CSHL ss3343272375 Nov 08, 2017 (151)
84 ILLUMINA ss3625523485 Oct 11, 2018 (152)
85 ILLUMINA ss3626006468 Oct 11, 2018 (152)
86 ILLUMINA ss3630505566 Oct 11, 2018 (152)
87 ILLUMINA ss3632878026 Oct 11, 2018 (152)
88 ILLUMINA ss3633571432 Oct 11, 2018 (152)
89 ILLUMINA ss3634301811 Oct 11, 2018 (152)
90 ILLUMINA ss3635265638 Oct 11, 2018 (152)
91 ILLUMINA ss3635978592 Oct 11, 2018 (152)
92 ILLUMINA ss3637015976 Oct 11, 2018 (152)
93 ILLUMINA ss3637732354 Oct 11, 2018 (152)
94 ILLUMINA ss3640009177 Oct 11, 2018 (152)
95 ILLUMINA ss3642746656 Oct 11, 2018 (152)
96 ILLUMINA ss3644477459 Oct 11, 2018 (152)
97 URBANLAB ss3646581171 Oct 11, 2018 (152)
98 EVA_DECODE ss3685991925 Jul 12, 2019 (153)
99 ACPOP ss3726716170 Jul 12, 2019 (153)
100 ILLUMINA ss3744040761 Jul 12, 2019 (153)
101 ILLUMINA ss3744602743 Jul 12, 2019 (153)
102 EVA ss3745720825 Jul 12, 2019 (153)
103 ILLUMINA ss3772104508 Jul 12, 2019 (153)
104 PACBIO ss3783302090 Jul 12, 2019 (153)
105 PACBIO ss3788979961 Jul 12, 2019 (153)
106 PACBIO ss3793852498 Jul 12, 2019 (153)
107 KHV_HUMAN_GENOMES ss3798743419 Jul 12, 2019 (153)
108 EVA ss3825981414 Apr 25, 2020 (154)
109 EVA ss3836378355 Apr 25, 2020 (154)
110 EVA ss3841782357 Apr 25, 2020 (154)
111 SGDP_PRJ ss3847994707 Apr 25, 2020 (154)
112 KRGDB ss3892835081 Apr 25, 2020 (154)
113 KOGIC ss3943629077 Apr 25, 2020 (154)
114 EVA ss3984450704 Apr 25, 2021 (155)
115 TOMMO_GENOMICS ss5142050932 Apr 25, 2021 (155)
116 1000Genomes NC_000001.10 - 752566 Oct 11, 2018 (152)
117 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 752566 Oct 11, 2018 (152)
118 Genome-wide autozygosity in Daghestan NC_000001.9 - 742429 Apr 25, 2020 (154)
119 The Danish reference pan genome NC_000001.10 - 752566 Apr 25, 2020 (154)
120 gnomAD - Genomes NC_000001.11 - 817186 Apr 25, 2021 (155)
121 Genome of the Netherlands Release 5 NC_000001.10 - 752566 Apr 25, 2020 (154)
122 HGDP-CEPH-db Supplement 1 NC_000001.9 - 742429 Apr 25, 2020 (154)
123 HapMap NC_000001.11 - 817186 Apr 25, 2020 (154)
124 KOREAN population from KRGDB NC_000001.10 - 752566 Apr 25, 2020 (154)
125 Korean Genome Project NC_000001.11 - 817186 Apr 25, 2020 (154)
126 Northern Sweden NC_000001.10 - 752566 Jul 12, 2019 (153)
127 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 752566 Apr 25, 2021 (155)
128 CNV burdens in cranial meningiomas NC_000001.10 - 752566 Apr 25, 2021 (155)
129 Qatari NC_000001.10 - 752566 Apr 25, 2020 (154)
130 SGDP_PRJ NC_000001.10 - 752566 Apr 25, 2020 (154)
131 Siberian NC_000001.10 - 752566 Apr 25, 2020 (154)
132 8.3KJPN NC_000001.10 - 752566 Apr 25, 2021 (155)
133 UK 10K study - Twins NC_000001.10 - 752566 Oct 11, 2018 (152)
134 A Vietnamese Genetic Variation Database NC_000001.10 - 752566 Jul 12, 2019 (153)
135 ALFA NC_000001.11 - 817186 Apr 25, 2021 (155)
Help

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, ss2147484243, ss2321502621, 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 NC_000001.10:752565:G:A NC_000001.11:817185:G:A (self)
60679, 40, 7078, 3644886641, ss3023513704, ss3066395614, ss3646581171, ss3685991925, ss3798743419, ss3841782357, ss3943629077 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, ss3066395615 NC_000001.11:817185:G:T NC_000001.11:817185:G:T (self)
Help

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
Help

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.

Software version is: 2.0.1.post596+ae089ad