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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.

rs1012583

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr3:150369221 (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
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.199634 (52841/264690, TOPMED)
A=0.253825 (51326/202210, ALFA)
A=0.207802 (29091/139994, GnomAD) (+ 20 more)
A=0.10776 (3045/28258, 14KJPN)
A=0.10626 (1781/16760, 8.3KJPN)
A=0.1947 (1247/6404, 1000G_30x)
A=0.1967 (985/5008, 1000G)
A=0.2636 (1181/4480, Estonian)
A=0.2675 (1031/3854, ALSPAC)
A=0.2775 (1029/3708, TWINSUK)
A=0.0657 (192/2922, KOREAN)
A=0.1843 (384/2084, HGDP_Stanford)
A=0.1638 (310/1892, HapMap)
A=0.0600 (110/1832, Korea1K)
A=0.273 (272/998, GoNL)
A=0.104 (82/792, PRJEB37584)
A=0.268 (161/600, NorthernSweden)
A=0.181 (39/216, Qatari)
A=0.093 (20/214, Vietnamese)
G=0.391 (72/184, SGDP_PRJ)
A=0.20 (8/40, GENOME_DK)
G=0.35 (7/20, Siberian)
A=0.22 (4/18, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 202210 G=0.746175 A=0.253825
European Sub 174932 G=0.741917 A=0.258083
African Sub 7094 G=0.8905 A=0.1095
African Others Sub 264 G=0.913 A=0.087
African American Sub 6830 G=0.8896 A=0.1104
Asian Sub 702 G=0.932 A=0.068
East Asian Sub 556 G=0.932 A=0.068
Other Asian Sub 146 G=0.932 A=0.068
Latin American 1 Sub 844 G=0.844 A=0.156
Latin American 2 Sub 6910 G=0.7402 A=0.2598
South Asian Sub 5042 G=0.6261 A=0.3739
Other Sub 6686 G=0.7694 A=0.2306


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=0.800366 A=0.199634
Allele Frequency Aggregator Total Global 202210 G=0.746175 A=0.253825
Allele Frequency Aggregator European Sub 174932 G=0.741917 A=0.258083
Allele Frequency Aggregator African Sub 7094 G=0.8905 A=0.1095
Allele Frequency Aggregator Latin American 2 Sub 6910 G=0.7402 A=0.2598
Allele Frequency Aggregator Other Sub 6686 G=0.7694 A=0.2306
Allele Frequency Aggregator South Asian Sub 5042 G=0.6261 A=0.3739
Allele Frequency Aggregator Latin American 1 Sub 844 G=0.844 A=0.156
Allele Frequency Aggregator Asian Sub 702 G=0.932 A=0.068
gnomAD - Genomes Global Study-wide 139994 G=0.792198 A=0.207802
gnomAD - Genomes European Sub 75802 G=0.73610 A=0.26390
gnomAD - Genomes African Sub 41956 G=0.88602 A=0.11398
gnomAD - Genomes American Sub 13634 G=0.77505 A=0.22495
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.8116 A=0.1884
gnomAD - Genomes East Asian Sub 3128 G=0.9357 A=0.0643
gnomAD - Genomes Other Sub 2152 G=0.8090 A=0.1910
14KJPN JAPANESE Study-wide 28258 G=0.89224 A=0.10776
8.3KJPN JAPANESE Study-wide 16760 G=0.89374 A=0.10626
1000Genomes_30x Global Study-wide 6404 G=0.8053 A=0.1947
1000Genomes_30x African Sub 1786 G=0.9031 A=0.0969
1000Genomes_30x Europe Sub 1266 G=0.7528 A=0.2472
1000Genomes_30x South Asian Sub 1202 G=0.6190 A=0.3810
1000Genomes_30x East Asian Sub 1170 G=0.9179 A=0.0821
1000Genomes_30x American Sub 980 G=0.789 A=0.211
1000Genomes Global Study-wide 5008 G=0.8033 A=0.1967
1000Genomes African Sub 1322 G=0.9002 A=0.0998
1000Genomes East Asian Sub 1008 G=0.9167 A=0.0833
1000Genomes Europe Sub 1006 G=0.7545 A=0.2455
1000Genomes South Asian Sub 978 G=0.620 A=0.380
1000Genomes American Sub 694 G=0.784 A=0.216
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.7364 A=0.2636
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.7325 A=0.2675
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.7225 A=0.2775
KOREAN population from KRGDB KOREAN Study-wide 2922 G=0.9343 A=0.0657
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.8157 A=0.1843
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.938 A=0.062
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.655 A=0.345
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.849 A=0.151
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.784 A=0.216
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.913 A=0.087
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.764 A=0.236
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.75 A=0.25
HapMap Global Study-wide 1892 G=0.8362 A=0.1638
HapMap American Sub 770 G=0.796 A=0.204
HapMap African Sub 692 G=0.880 A=0.120
HapMap Asian Sub 254 G=0.890 A=0.110
HapMap Europe Sub 176 G=0.761 A=0.239
Korean Genome Project KOREAN Study-wide 1832 G=0.9400 A=0.0600
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.727 A=0.273
CNV burdens in cranial meningiomas Global Study-wide 792 G=0.896 A=0.104
CNV burdens in cranial meningiomas CRM Sub 792 G=0.896 A=0.104
Northern Sweden ACPOP Study-wide 600 G=0.732 A=0.268
Qatari Global Study-wide 216 G=0.819 A=0.181
A Vietnamese Genetic Variation Database Global Study-wide 214 G=0.907 A=0.093
SGDP_PRJ Global Study-wide 184 G=0.391 A=0.609
The Danish reference pan genome Danish Study-wide 40 G=0.80 A=0.20
Siberian Global Study-wide 20 G=0.35 A=0.65
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 18 G=0.78 A=0.22
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 3 NC_000003.12:g.150369221G>A
GRCh37.p13 chr 3 NC_000003.11:g.150087008G>A
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
GRCh38.p14 chr 3 NC_000003.12:g.150369221= NC_000003.12:g.150369221G>A
GRCh37.p13 chr 3 NC_000003.11:g.150087008= NC_000003.11:g.150087008G>A
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, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1475671 Oct 05, 2000 (86)
2 ABI ss44392874 Mar 15, 2006 (126)
3 ILLUMINA ss66729036 Dec 01, 2006 (127)
4 ILLUMINA ss66871301 Dec 01, 2006 (127)
5 ILLUMINA ss66949284 Dec 01, 2006 (127)
6 ILLUMINA ss70359693 May 17, 2007 (127)
7 ILLUMINA ss70466787 May 26, 2008 (130)
8 ILLUMINA ss70988115 May 17, 2007 (127)
9 ILLUMINA ss75687576 Dec 07, 2007 (129)
10 HGSV ss77298912 Dec 07, 2007 (129)
11 KRIBB_YJKIM ss83657167 Dec 15, 2007 (130)
12 1000GENOMES ss112573562 Jan 25, 2009 (130)
13 ILLUMINA ss121270023 Dec 01, 2009 (131)
14 ILLUMINA ss152578109 Dec 01, 2009 (131)
15 ILLUMINA ss159110820 Dec 01, 2009 (131)
16 ILLUMINA ss159866885 Dec 01, 2009 (131)
17 ILLUMINA ss169275615 Jul 04, 2010 (132)
18 ILLUMINA ss169712766 Jul 04, 2010 (132)
19 BCM-HGSC-SUB ss206175393 Jul 04, 2010 (132)
20 ILLUMINA ss209083036 Jul 04, 2010 (132)
21 1000GENOMES ss220498754 Jul 14, 2010 (132)
22 1000GENOMES ss232084352 Jul 14, 2010 (132)
23 1000GENOMES ss239444249 Jul 15, 2010 (132)
24 GMI ss277400001 May 04, 2012 (137)
25 GMI ss284771885 Apr 25, 2013 (138)
26 ILLUMINA ss479195877 May 04, 2012 (137)
27 ILLUMINA ss479198292 May 04, 2012 (137)
28 ILLUMINA ss479533853 Sep 08, 2015 (146)
29 ILLUMINA ss484398946 May 04, 2012 (137)
30 ILLUMINA ss536579388 Sep 08, 2015 (146)
31 TISHKOFF ss557026844 Apr 25, 2013 (138)
32 SSMP ss650758830 Apr 25, 2013 (138)
33 ILLUMINA ss778723844 Sep 08, 2015 (146)
34 ILLUMINA ss782645843 Sep 08, 2015 (146)
35 ILLUMINA ss783615182 Sep 08, 2015 (146)
36 ILLUMINA ss825329424 Apr 01, 2015 (144)
37 ILLUMINA ss831896118 Sep 08, 2015 (146)
38 ILLUMINA ss832623583 Jul 13, 2019 (153)
39 ILLUMINA ss834183265 Sep 08, 2015 (146)
40 EVA-GONL ss979299934 Aug 21, 2014 (142)
41 JMKIDD_LAB ss1070936474 Aug 21, 2014 (142)
42 1000GENOMES ss1306691337 Aug 21, 2014 (142)
43 DDI ss1429628300 Apr 01, 2015 (144)
44 EVA_GENOME_DK ss1580235800 Apr 01, 2015 (144)
45 EVA_DECODE ss1588791411 Apr 01, 2015 (144)
46 EVA_UK10K_ALSPAC ss1608495658 Apr 01, 2015 (144)
47 EVA_UK10K_TWINSUK ss1651489691 Apr 01, 2015 (144)
48 EVA_SVP ss1712622069 Apr 01, 2015 (144)
49 ILLUMINA ss1752446533 Sep 08, 2015 (146)
50 WEILL_CORNELL_DGM ss1922523228 Feb 12, 2016 (147)
51 GENOMED ss1969553738 Jul 19, 2016 (147)
52 JJLAB ss2021833250 Sep 14, 2016 (149)
53 ILLUMINA ss2095138700 Dec 20, 2016 (150)
54 USC_VALOUEV ss2149929710 Dec 20, 2016 (150)
55 HUMAN_LONGEVITY ss2256938536 Dec 20, 2016 (150)
56 ILLUMINA ss2634028130 Nov 08, 2017 (151)
57 GRF ss2705343286 Nov 08, 2017 (151)
58 GNOMAD ss2800651447 Nov 08, 2017 (151)
59 SWEGEN ss2993408856 Nov 08, 2017 (151)
60 ILLUMINA ss3022300294 Nov 08, 2017 (151)
61 BIOINF_KMB_FNS_UNIBA ss3024684130 Nov 08, 2017 (151)
62 CSHL ss3345327929 Nov 08, 2017 (151)
63 ILLUMINA ss3628805799 Oct 12, 2018 (152)
64 ILLUMINA ss3631970123 Oct 12, 2018 (152)
65 ILLUMINA ss3633313066 Oct 12, 2018 (152)
66 ILLUMINA ss3634030982 Oct 12, 2018 (152)
67 ILLUMINA ss3634923109 Oct 12, 2018 (152)
68 ILLUMINA ss3635714453 Oct 12, 2018 (152)
69 ILLUMINA ss3636620491 Oct 12, 2018 (152)
70 ILLUMINA ss3637466881 Oct 12, 2018 (152)
71 ILLUMINA ss3638449238 Oct 12, 2018 (152)
72 ILLUMINA ss3639227374 Oct 12, 2018 (152)
73 ILLUMINA ss3639632920 Oct 12, 2018 (152)
74 ILLUMINA ss3640630407 Oct 12, 2018 (152)
75 ILLUMINA ss3643403564 Oct 12, 2018 (152)
76 ILLUMINA ss3652779914 Oct 12, 2018 (152)
77 EGCUT_WGS ss3661341354 Jul 13, 2019 (153)
78 EVA_DECODE ss3710547755 Jul 13, 2019 (153)
79 ILLUMINA ss3726069478 Jul 13, 2019 (153)
80 ACPOP ss3730466331 Jul 13, 2019 (153)
81 ILLUMINA ss3745223083 Jul 13, 2019 (153)
82 EVA ss3760856001 Jul 13, 2019 (153)
83 ILLUMINA ss3772718272 Jul 13, 2019 (153)
84 PACBIO ss3784499523 Jul 13, 2019 (153)
85 PACBIO ss3789987614 Jul 13, 2019 (153)
86 PACBIO ss3794862220 Jul 13, 2019 (153)
87 KHV_HUMAN_GENOMES ss3803990641 Jul 13, 2019 (153)
88 EVA ss3828140859 Apr 25, 2020 (154)
89 HGDP ss3847728020 Apr 25, 2020 (154)
90 SGDP_PRJ ss3857250317 Apr 25, 2020 (154)
91 KRGDB ss3903290065 Apr 25, 2020 (154)
92 KOGIC ss3952670077 Apr 25, 2020 (154)
93 EVA ss3984517180 Apr 26, 2021 (155)
94 EVA ss3985029166 Apr 26, 2021 (155)
95 EVA ss4017112632 Apr 26, 2021 (155)
96 TOPMED ss4588274895 Apr 26, 2021 (155)
97 TOMMO_GENOMICS ss5162181843 Apr 26, 2021 (155)
98 EVA ss5237334811 Apr 26, 2021 (155)
99 1000G_HIGH_COVERAGE ss5256491487 Oct 12, 2022 (156)
100 EVA ss5314902876 Oct 12, 2022 (156)
101 EVA ss5344122416 Oct 12, 2022 (156)
102 HUGCELL_USP ss5455583933 Oct 12, 2022 (156)
103 1000G_HIGH_COVERAGE ss5536173779 Oct 12, 2022 (156)
104 SANFORD_IMAGENETICS ss5624534689 Oct 12, 2022 (156)
105 SANFORD_IMAGENETICS ss5633454146 Oct 12, 2022 (156)
106 TOMMO_GENOMICS ss5695233060 Oct 12, 2022 (156)
107 EVA ss5799596164 Oct 12, 2022 (156)
108 YY_MCH ss5804361342 Oct 12, 2022 (156)
109 EVA ss5826658652 Oct 12, 2022 (156)
110 EVA ss5847228547 Oct 12, 2022 (156)
111 EVA ss5847986362 Oct 12, 2022 (156)
112 EVA ss5853893122 Oct 12, 2022 (156)
113 EVA ss5871537899 Oct 12, 2022 (156)
114 EVA ss5961816125 Oct 12, 2022 (156)
115 EVA ss5979675807 Oct 12, 2022 (156)
116 1000Genomes NC_000003.11 - 150087008 Oct 12, 2018 (152)
117 1000Genomes_30x NC_000003.12 - 150369221 Oct 12, 2022 (156)
118 The Avon Longitudinal Study of Parents and Children NC_000003.11 - 150087008 Oct 12, 2018 (152)
119 Genetic variation in the Estonian population NC_000003.11 - 150087008 Oct 12, 2018 (152)
120 The Danish reference pan genome NC_000003.11 - 150087008 Apr 25, 2020 (154)
121 gnomAD - Genomes NC_000003.12 - 150369221 Apr 26, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000003.11 - 150087008 Apr 25, 2020 (154)
123 HGDP-CEPH-db Supplement 1 NC_000003.10 - 151569698 Apr 25, 2020 (154)
124 HapMap NC_000003.12 - 150369221 Apr 25, 2020 (154)
125 KOREAN population from KRGDB NC_000003.11 - 150087008 Apr 25, 2020 (154)
126 Korean Genome Project NC_000003.12 - 150369221 Apr 25, 2020 (154)
127 Northern Sweden NC_000003.11 - 150087008 Jul 13, 2019 (153)
128 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000003.11 - 150087008 Apr 26, 2021 (155)
129 CNV burdens in cranial meningiomas NC_000003.11 - 150087008 Apr 26, 2021 (155)
130 Qatari NC_000003.11 - 150087008 Apr 25, 2020 (154)
131 SGDP_PRJ NC_000003.11 - 150087008 Apr 25, 2020 (154)
132 Siberian NC_000003.11 - 150087008 Apr 25, 2020 (154)
133 8.3KJPN NC_000003.11 - 150087008 Apr 26, 2021 (155)
134 14KJPN NC_000003.12 - 150369221 Oct 12, 2022 (156)
135 TopMed NC_000003.12 - 150369221 Apr 26, 2021 (155)
136 UK 10K study - Twins NC_000003.11 - 150087008 Oct 12, 2018 (152)
137 A Vietnamese Genetic Variation Database NC_000003.11 - 150087008 Jul 13, 2019 (153)
138 ALFA NC_000003.12 - 150369221 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)
rs60639958 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss77298912, ss3639227374, ss3639632920 NC_000003.9:151569705:G:A NC_000003.12:150369220:G:A (self)
405912, ss112573562, ss206175393, ss277400001, ss284771885, ss479195877, ss825329424, ss1588791411, ss1712622069, ss3643403564, ss3847728020 NC_000003.10:151569697:G:A NC_000003.12:150369220:G:A (self)
17973992, 10011543, 7079602, 6400739, 4398275, 10467459, 3751196, 255093, 66531, 4565158, 9267297, 2446064, 20151150, 10011543, 2183945, ss220498754, ss232084352, ss239444249, ss479198292, ss479533853, ss484398946, ss536579388, ss557026844, ss650758830, ss778723844, ss782645843, ss783615182, ss831896118, ss832623583, ss834183265, ss979299934, ss1070936474, ss1306691337, ss1429628300, ss1580235800, ss1608495658, ss1651489691, ss1752446533, ss1922523228, ss1969553738, ss2021833250, ss2095138700, ss2149929710, ss2634028130, ss2705343286, ss2800651447, ss2993408856, ss3022300294, ss3345327929, ss3628805799, ss3631970123, ss3633313066, ss3634030982, ss3634923109, ss3635714453, ss3636620491, ss3637466881, ss3638449238, ss3640630407, ss3652779914, ss3661341354, ss3730466331, ss3745223083, ss3760856001, ss3772718272, ss3784499523, ss3789987614, ss3794862220, ss3828140859, ss3857250317, ss3903290065, ss3984517180, ss3985029166, ss4017112632, ss5162181843, ss5237334811, ss5314902876, ss5344122416, ss5624534689, ss5633454146, ss5799596164, ss5826658652, ss5847228547, ss5847986362, ss5961816125, ss5979675807 NC_000003.11:150087007:G:A NC_000003.12:150369220:G:A (self)
23699714, 127686060, 2482844, 9048078, 29070164, 425652450, 10037224156, ss2256938536, ss3024684130, ss3710547755, ss3726069478, ss3803990641, ss3952670077, ss4588274895, ss5256491487, ss5455583933, ss5536173779, ss5695233060, ss5804361342, ss5853893122, ss5871537899 NC_000003.12:150369220:G:A NC_000003.12:150369220:G:A (self)
ss1475671, ss44392874, ss66729036, ss66871301, ss66949284, ss70359693, ss70466787, ss70988115, ss75687576, ss83657167, ss121270023, ss152578109, ss159110820, ss159866885, ss169275615, ss169712766, ss209083036 NT_005612.16:56582153:G:A NC_000003.12:150369220:G:A (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 rs1012583

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.post761+d5e8e07