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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs2303879

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:27527746 (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>C / G>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.337829 (89420/264690, TOPMED)
G=0.359070 (50287/140048, GnomAD)
G=0.25393 (19984/78698, PAGE_STUDY) (+ 18 more)
G=0.22227 (6281/28258, 14KJPN)
G=0.22774 (3817/16760, 8.3KJPN)
G=0.49308 (7264/14732, ALFA)
G=0.3042 (1948/6404, 1000G_30x)
G=0.3095 (1550/5008, 1000G)
G=0.4911 (2200/4480, Estonian)
G=0.4730 (1823/3854, ALSPAC)
G=0.4887 (1812/3708, TWINSUK)
G=0.2041 (598/2930, KOREAN)
G=0.2646 (497/1878, HapMap)
G=0.481 (480/998, GoNL)
G=0.463 (278/600, NorthernSweden)
G=0.478 (255/534, MGP)
G=0.244 (113/464, SGDP_PRJ)
G=0.384 (83/216, Qatari)
G=0.364 (78/214, Vietnamese)
G=0.23 (11/48, Siberian)
G=0.38 (15/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
GABRG3 : 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 14732 G=0.49308 A=0.50692
European Sub 9902 G=0.5850 A=0.4150
African Sub 1228 G=0.2199 A=0.7801
African Others Sub 12 G=0.17 A=0.83
African American Sub 1216 G=0.2204 A=0.7796
Asian Sub 98 G=0.52 A=0.48
East Asian Sub 62 G=0.40 A=0.60
Other Asian Sub 36 G=0.72 A=0.28
Latin American 1 Sub 170 G=0.453 A=0.547
Latin American 2 Sub 2184 G=0.3027 A=0.6973
South Asian Sub 38 G=0.76 A=0.24
Other Sub 1112 G=0.3444 A=0.6556


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
TopMed Global Study-wide 264690 G=0.337829 A=0.662171
gnomAD - Genomes Global Study-wide 140048 G=0.359070 A=0.640930
gnomAD - Genomes European Sub 75836 G=0.47268 A=0.52732
gnomAD - Genomes African Sub 41978 G=0.16406 A=0.83594
gnomAD - Genomes American Sub 13642 G=0.32876 A=0.67124
gnomAD - Genomes Ashkenazi Jewish Sub 3320 G=0.3849 A=0.6151
gnomAD - Genomes East Asian Sub 3118 G=0.3153 A=0.6847
gnomAD - Genomes Other Sub 2154 G=0.3751 A=0.6249
The PAGE Study Global Study-wide 78698 G=0.25393 A=0.74607
The PAGE Study AfricanAmerican Sub 32512 G=0.17052 A=0.82948
The PAGE Study Mexican Sub 10810 G=0.27438 A=0.72562
The PAGE Study Asian Sub 8318 G=0.2644 A=0.7356
The PAGE Study PuertoRican Sub 7918 G=0.3260 A=0.6740
The PAGE Study NativeHawaiian Sub 4534 G=0.4365 A=0.5635
The PAGE Study Cuban Sub 4230 G=0.3742 A=0.6258
The PAGE Study Dominican Sub 3828 G=0.2824 A=0.7176
The PAGE Study CentralAmerican Sub 2450 G=0.2498 A=0.7502
The PAGE Study SouthAmerican Sub 1982 G=0.3113 A=0.6887
The PAGE Study NativeAmerican Sub 1260 G=0.3595 A=0.6405
The PAGE Study SouthAsian Sub 856 G=0.431 A=0.569
14KJPN JAPANESE Study-wide 28258 G=0.22227 A=0.77773
8.3KJPN JAPANESE Study-wide 16760 G=0.22774 A=0.77226
Allele Frequency Aggregator Total Global 14732 G=0.49308 A=0.50692
Allele Frequency Aggregator European Sub 9902 G=0.5850 A=0.4150
Allele Frequency Aggregator Latin American 2 Sub 2184 G=0.3027 A=0.6973
Allele Frequency Aggregator African Sub 1228 G=0.2199 A=0.7801
Allele Frequency Aggregator Other Sub 1112 G=0.3444 A=0.6556
Allele Frequency Aggregator Latin American 1 Sub 170 G=0.453 A=0.547
Allele Frequency Aggregator Asian Sub 98 G=0.52 A=0.48
Allele Frequency Aggregator South Asian Sub 38 G=0.76 A=0.24
1000Genomes_30x Global Study-wide 6404 G=0.3042 A=0.6958
1000Genomes_30x African Sub 1786 G=0.0985 A=0.9015
1000Genomes_30x Europe Sub 1266 G=0.4581 A=0.5419
1000Genomes_30x South Asian Sub 1202 G=0.4775 A=0.5225
1000Genomes_30x East Asian Sub 1170 G=0.3128 A=0.6872
1000Genomes_30x American Sub 980 G=0.257 A=0.743
1000Genomes Global Study-wide 5008 G=0.3095 A=0.6905
1000Genomes African Sub 1322 G=0.0998 A=0.9002
1000Genomes East Asian Sub 1008 G=0.3105 A=0.6895
1000Genomes Europe Sub 1006 G=0.4493 A=0.5507
1000Genomes South Asian Sub 978 G=0.487 A=0.513
1000Genomes American Sub 694 G=0.255 A=0.745
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.4911 A=0.5089
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.4730 A=0.5270
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.4887 A=0.5113
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.2041 A=0.7959, C=0.0000, T=0.0000
HapMap Global Study-wide 1878 G=0.2646 A=0.7354
HapMap American Sub 762 G=0.356 A=0.644
HapMap African Sub 686 G=0.121 A=0.879
HapMap Asian Sub 254 G=0.283 A=0.717
HapMap Europe Sub 176 G=0.403 A=0.597
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.481 A=0.519
Northern Sweden ACPOP Study-wide 600 G=0.463 A=0.537
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.478 A=0.522
SGDP_PRJ Global Study-wide 464 G=0.244 A=0.756
Qatari Global Study-wide 216 G=0.384 A=0.616
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.364 A=0.636
Siberian Global Study-wide 48 G=0.23 A=0.77
The Danish reference pan genome Danish Study-wide 40 G=0.38 A=0.62
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.p14 chr 15 NC_000015.10:g.27527746G>A
GRCh38.p14 chr 15 NC_000015.10:g.27527746G>C
GRCh38.p14 chr 15 NC_000015.10:g.27527746G>T
GRCh37.p13 chr 15 NC_000015.9:g.27772892G>A
GRCh37.p13 chr 15 NC_000015.9:g.27772892G>C
GRCh37.p13 chr 15 NC_000015.9:g.27772892G>T
GABRG3 RefSeqGene NG_032887.2:g.561566G>A
GABRG3 RefSeqGene NG_032887.2:g.561566G>C
GABRG3 RefSeqGene NG_032887.2:g.561566G>T
Gene: GABRG3, gamma-aminobutyric acid type A receptor subunit gamma3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
GABRG3 transcript variant 1 NM_033223.5:c.1062+117G>A N/A Intron Variant
GABRG3 transcript variant 2 NM_001270873.2:c. N/A Genic Downstream 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
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 C T
GRCh38.p14 chr 15 NC_000015.10:g.27527746= NC_000015.10:g.27527746G>A NC_000015.10:g.27527746G>C NC_000015.10:g.27527746G>T
GRCh37.p13 chr 15 NC_000015.9:g.27772892= NC_000015.9:g.27772892G>A NC_000015.9:g.27772892G>C NC_000015.9:g.27772892G>T
GABRG3 RefSeqGene NG_032887.2:g.561566= NG_032887.2:g.561566G>A NG_032887.2:g.561566G>C NG_032887.2:g.561566G>T
GABRG3 transcript variant 1 NM_033223.4:c.1062+117= NM_033223.4:c.1062+117G>A NM_033223.4:c.1062+117G>C NM_033223.4:c.1062+117G>T
GABRG3 transcript variant 1 NM_033223.5:c.1062+117= NM_033223.5:c.1062+117G>A NM_033223.5:c.1062+117G>C NM_033223.5:c.1062+117G>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#.

95 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 YUSUKE ss3250621 Sep 28, 2001 (100)
2 SC_JCM ss4334087 Mar 26, 2002 (103)
3 WI_SSAHASNP ss12313375 Jul 11, 2003 (116)
4 CSHL-HAPMAP ss17532562 Feb 27, 2004 (120)
5 SSAHASNP ss21239950 Apr 05, 2004 (121)
6 PERLEGEN ss24674823 Sep 20, 2004 (123)
7 ABI ss43723600 Mar 15, 2006 (126)
8 SI_EXO ss52075585 Oct 15, 2006 (127)
9 AFFY ss66268258 Nov 30, 2006 (127)
10 PERLEGEN ss69171313 May 17, 2007 (127)
11 AFFY ss76413257 Dec 08, 2007 (129)
12 KRIBB_YJKIM ss81758402 Dec 14, 2007 (130)
13 HGSV ss83163665 Dec 14, 2007 (130)
14 BCMHGSC_JDW ss90102730 Mar 24, 2008 (129)
15 HUMANGENOME_JCVI ss96799504 Feb 03, 2009 (130)
16 BGI ss103224026 Dec 01, 2009 (131)
17 1000GENOMES ss108691915 Jan 23, 2009 (130)
18 1000GENOMES ss113946779 Jan 25, 2009 (130)
19 ILLUMINA-UK ss118170039 Feb 14, 2009 (130)
20 ENSEMBL ss132383026 Dec 01, 2009 (131)
21 ENSEMBL ss134208517 Dec 01, 2009 (131)
22 GMI ss156353718 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss167710192 Jul 04, 2010 (132)
24 COMPLETE_GENOMICS ss168971870 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss170878061 Jul 04, 2010 (132)
26 AFFY ss173508361 Jul 04, 2010 (132)
27 BUSHMAN ss200647341 Jul 04, 2010 (132)
28 BCM-HGSC-SUB ss207203698 Jul 04, 2010 (132)
29 1000GENOMES ss226810468 Jul 14, 2010 (132)
30 1000GENOMES ss236720932 Jul 15, 2010 (132)
31 1000GENOMES ss243119332 Jul 15, 2010 (132)
32 BL ss254858452 May 09, 2011 (134)
33 GMI ss282191306 May 04, 2012 (137)
34 GMI ss286923821 Apr 25, 2013 (138)
35 PJP ss291807383 May 09, 2011 (134)
36 TISHKOFF ss564380417 Apr 25, 2013 (138)
37 SSMP ss660092931 Apr 25, 2013 (138)
38 EVA-GONL ss991620373 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1079999669 Aug 21, 2014 (142)
40 1000GENOMES ss1352805074 Aug 21, 2014 (142)
41 DDI ss1427574539 Apr 01, 2015 (144)
42 EVA_GENOME_DK ss1577520691 Apr 01, 2015 (144)
43 EVA_UK10K_ALSPAC ss1632662765 Apr 01, 2015 (144)
44 EVA_UK10K_TWINSUK ss1675656798 Apr 01, 2015 (144)
45 EVA_DECODE ss1695631683 Apr 01, 2015 (144)
46 EVA_MGP ss1711390012 Apr 01, 2015 (144)
47 EVA_SVP ss1713477266 Apr 01, 2015 (144)
48 HAMMER_LAB ss1808128841 Sep 08, 2015 (146)
49 WEILL_CORNELL_DGM ss1935017306 Feb 12, 2016 (147)
50 ILLUMINA ss1959597107 Feb 12, 2016 (147)
51 GENOMED ss1968069523 Jul 19, 2016 (147)
52 JJLAB ss2028288843 Sep 14, 2016 (149)
53 USC_VALOUEV ss2156685711 Dec 20, 2016 (150)
54 HUMAN_LONGEVITY ss2205495865 Dec 20, 2016 (150)
55 SYSTEMSBIOZJU ss2628637329 Nov 08, 2017 (151)
56 GRF ss2701144647 Nov 08, 2017 (151)
57 GNOMAD ss2932943908 Nov 08, 2017 (151)
58 SWEGEN ss3013000325 Nov 08, 2017 (151)
59 ILLUMINA ss3021615797 Nov 08, 2017 (151)
60 BIOINF_KMB_FNS_UNIBA ss3027968500 Nov 08, 2017 (151)
61 CSHL ss3351040100 Nov 08, 2017 (151)
62 URBANLAB ss3650316171 Oct 12, 2018 (152)
63 ILLUMINA ss3652015099 Oct 12, 2018 (152)
64 EGCUT_WGS ss3680171256 Jul 13, 2019 (153)
65 EVA_DECODE ss3697576883 Jul 13, 2019 (153)
66 ILLUMINA ss3725484345 Jul 13, 2019 (153)
67 ACPOP ss3740783923 Jul 13, 2019 (153)
68 EVA ss3752886383 Jul 13, 2019 (153)
69 PAGE_CC ss3771818149 Jul 13, 2019 (153)
70 KHV_HUMAN_GENOMES ss3818203574 Jul 13, 2019 (153)
71 EVA ss3834154343 Apr 27, 2020 (154)
72 EVA ss3840673910 Apr 27, 2020 (154)
73 EVA ss3846162655 Apr 27, 2020 (154)
74 SGDP_PRJ ss3882543345 Apr 27, 2020 (154)
75 KRGDB ss3931667730 Apr 27, 2020 (154)
76 FSA-LAB ss3984068205 Apr 26, 2021 (155)
77 EVA ss3986639049 Apr 26, 2021 (155)
78 TOPMED ss4985587506 Apr 26, 2021 (155)
79 TOMMO_GENOMICS ss5215388252 Apr 26, 2021 (155)
80 EVA ss5237228901 Apr 26, 2021 (155)
81 1000G_HIGH_COVERAGE ss5297846477 Oct 17, 2022 (156)
82 EVA ss5418168890 Oct 17, 2022 (156)
83 HUGCELL_USP ss5491663633 Oct 17, 2022 (156)
84 1000G_HIGH_COVERAGE ss5598950706 Oct 17, 2022 (156)
85 EVA ss5624050685 Oct 17, 2022 (156)
86 SANFORD_IMAGENETICS ss5657166999 Oct 17, 2022 (156)
87 TOMMO_GENOMICS ss5768958596 Oct 17, 2022 (156)
88 EVA ss5800191612 Oct 17, 2022 (156)
89 YY_MCH ss5815185107 Oct 17, 2022 (156)
90 EVA ss5827977804 Oct 17, 2022 (156)
91 EVA ss5848396444 Oct 17, 2022 (156)
92 EVA ss5851225782 Oct 17, 2022 (156)
93 EVA ss5875233534 Oct 17, 2022 (156)
94 EVA ss5936559586 Oct 17, 2022 (156)
95 EVA ss5948577500 Oct 17, 2022 (156)
96 1000Genomes NC_000015.9 - 27772892 Oct 12, 2018 (152)
97 1000Genomes_30x NC_000015.10 - 27527746 Oct 17, 2022 (156)
98 The Avon Longitudinal Study of Parents and Children NC_000015.9 - 27772892 Oct 12, 2018 (152)
99 Genetic variation in the Estonian population NC_000015.9 - 27772892 Oct 12, 2018 (152)
100 The Danish reference pan genome NC_000015.9 - 27772892 Apr 27, 2020 (154)
101 gnomAD - Genomes NC_000015.10 - 27527746 Apr 26, 2021 (155)
102 Genome of the Netherlands Release 5 NC_000015.9 - 27772892 Apr 27, 2020 (154)
103 HapMap NC_000015.10 - 27527746 Apr 27, 2020 (154)
104 KOREAN population from KRGDB NC_000015.9 - 27772892 Apr 27, 2020 (154)
105 Medical Genome Project healthy controls from Spanish population NC_000015.9 - 27772892 Apr 27, 2020 (154)
106 Northern Sweden NC_000015.9 - 27772892 Jul 13, 2019 (153)
107 The PAGE Study NC_000015.10 - 27527746 Jul 13, 2019 (153)
108 Qatari NC_000015.9 - 27772892 Apr 27, 2020 (154)
109 SGDP_PRJ NC_000015.9 - 27772892 Apr 27, 2020 (154)
110 Siberian NC_000015.9 - 27772892 Apr 27, 2020 (154)
111 8.3KJPN NC_000015.9 - 27772892 Apr 26, 2021 (155)
112 14KJPN NC_000015.10 - 27527746 Oct 17, 2022 (156)
113 TopMed NC_000015.10 - 27527746 Apr 26, 2021 (155)
114 UK 10K study - Twins NC_000015.9 - 27772892 Oct 12, 2018 (152)
115 A Vietnamese Genetic Variation Database NC_000015.9 - 27772892 Jul 13, 2019 (153)
116 ALFA NC_000015.10 - 27527746 Apr 26, 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)
rs17564058 Oct 08, 2004 (123)
rs56871230 May 23, 2008 (130)
rs57965485 Feb 26, 2009 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss83163665, ss90102730, ss108691915, ss113946779, ss118170039, ss167710192, ss168971870, ss170878061, ss200647341, ss207203698, ss254858452, ss282191306, ss286923821, ss291807383, ss1695631683, ss1713477266 NC_000015.8:25446486:G:A NC_000015.10:27527745:G:A (self)
65851604, 36565938, 25909504, 3790942, 16334369, 38845124, 505772, 14068788, 17059236, 34560325, 9202065, 73357559, 36565938, 8135849, ss226810468, ss236720932, ss243119332, ss564380417, ss660092931, ss991620373, ss1079999669, ss1352805074, ss1427574539, ss1577520691, ss1632662765, ss1675656798, ss1711390012, ss1808128841, ss1935017306, ss1959597107, ss1968069523, ss2028288843, ss2156685711, ss2628637329, ss2701144647, ss2932943908, ss3013000325, ss3021615797, ss3351040100, ss3652015099, ss3680171256, ss3740783923, ss3752886383, ss3834154343, ss3840673910, ss3882543345, ss3931667730, ss3984068205, ss3986639049, ss5215388252, ss5418168890, ss5624050685, ss5657166999, ss5800191612, ss5827977804, ss5848396444, ss5936559586, ss5948577500 NC_000015.9:27772891:G:A NC_000015.10:27527745:G:A (self)
86476641, 464167353, 1231606, 1039618, 102795700, 201133166, 5055707325, ss2205495865, ss3027968500, ss3650316171, ss3697576883, ss3725484345, ss3771818149, ss3818203574, ss3846162655, ss4985587506, ss5237228901, ss5297846477, ss5491663633, ss5598950706, ss5768958596, ss5815185107, ss5851225782, ss5875233534 NC_000015.10:27527745:G:A NC_000015.10:27527745:G:A (self)
ss12313375 NT_010280.15:138382:G:A NC_000015.10:27527745:G:A (self)
ss17532562, ss21239950 NT_010280.16:138382:G:A NC_000015.10:27527745:G:A (self)
ss52075585 NT_010280.17:175880:G:A NC_000015.10:27527745:G:A (self)
ss3250621, ss4334087, ss24674823, ss43723600, ss66268258, ss69171313, ss76413257, ss81758402, ss96799504, ss103224026, ss132383026, ss134208517, ss156353718, ss173508361 NT_026446.14:4208038:G:A NC_000015.10:27527745:G:A (self)
38845124, ss3931667730 NC_000015.9:27772891:G:C NC_000015.10:27527745:G:C (self)
38845124, ss3931667730 NC_000015.9:27772891:G:T NC_000015.10:27527745: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.

No publications for rs2303879

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.post774+babeb33