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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.

rs11125375

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:51725011 (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=0.405811 (107414/264690, TOPMED)
G=0.393463 (54992/139764, GnomAD)
G=0.34493 (25331/73438, ALFA) (+ 20 more)
G=0.44179 (12484/28258, 14KJPN)
G=0.43807 (7342/16760, 8.3KJPN)
G=0.4283 (2743/6404, 1000G_30x)
G=0.4231 (2119/5008, 1000G)
G=0.2871 (1286/4480, Estonian)
G=0.3298 (1271/3854, ALSPAC)
G=0.3328 (1234/3708, TWINSUK)
G=0.4334 (1270/2930, KOREAN)
G=0.4016 (837/2084, HGDP_Stanford)
G=0.4760 (891/1872, HapMap)
G=0.4088 (749/1832, Korea1K)
G=0.329 (328/998, GoNL)
G=0.389 (305/784, PRJEB37584)
G=0.348 (209/600, NorthernSweden)
G=0.271 (116/428, SGDP_PRJ)
G=0.403 (87/216, Qatari)
G=0.425 (90/212, Vietnamese)
G=0.28 (13/46, Siberian)
G=0.30 (12/40, GENOME_DK)
G=0.00 (0/20, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LOC730100 : Intron 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 73438 G=0.34493 A=0.65507
European Sub 57464 G=0.32119 A=0.67881
African Sub 5006 G=0.5310 A=0.4690
African Others Sub 180 G=0.567 A=0.433
African American Sub 4826 G=0.5296 A=0.4704
Asian Sub 238 G=0.374 A=0.626
East Asian Sub 164 G=0.421 A=0.579
Other Asian Sub 74 G=0.27 A=0.73
Latin American 1 Sub 398 G=0.377 A=0.623
Latin American 2 Sub 3310 G=0.3958 A=0.6042
South Asian Sub 4966 G=0.3794 A=0.6206
Other Sub 2056 G=0.3808 A=0.6192


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=0.405811 A=0.594189
gnomAD - Genomes Global Study-wide 139764 G=0.393463 A=0.606537
gnomAD - Genomes European Sub 75764 G=0.32098 A=0.67902
gnomAD - Genomes African Sub 41870 G=0.53380 A=0.46620
gnomAD - Genomes American Sub 13550 G=0.38251 A=0.61749
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=0.3001 A=0.6999
gnomAD - Genomes East Asian Sub 3122 G=0.4238 A=0.5762
gnomAD - Genomes Other Sub 2136 G=0.3839 A=0.6161
Allele Frequency Aggregator Total Global 73438 G=0.34493 A=0.65507
Allele Frequency Aggregator European Sub 57464 G=0.32119 A=0.67881
Allele Frequency Aggregator African Sub 5006 G=0.5310 A=0.4690
Allele Frequency Aggregator South Asian Sub 4966 G=0.3794 A=0.6206
Allele Frequency Aggregator Latin American 2 Sub 3310 G=0.3958 A=0.6042
Allele Frequency Aggregator Other Sub 2056 G=0.3808 A=0.6192
Allele Frequency Aggregator Latin American 1 Sub 398 G=0.377 A=0.623
Allele Frequency Aggregator Asian Sub 238 G=0.374 A=0.626
14KJPN JAPANESE Study-wide 28258 G=0.44179 A=0.55821
8.3KJPN JAPANESE Study-wide 16760 G=0.43807 A=0.56193
1000Genomes_30x Global Study-wide 6404 G=0.4283 A=0.5717
1000Genomes_30x African Sub 1786 G=0.5722 A=0.4278
1000Genomes_30x Europe Sub 1266 G=0.3049 A=0.6951
1000Genomes_30x South Asian Sub 1202 G=0.3644 A=0.6356
1000Genomes_30x East Asian Sub 1170 G=0.4299 A=0.5701
1000Genomes_30x American Sub 980 G=0.402 A=0.598
1000Genomes Global Study-wide 5008 G=0.4231 A=0.5769
1000Genomes African Sub 1322 G=0.5764 A=0.4236
1000Genomes East Asian Sub 1008 G=0.4325 A=0.5675
1000Genomes Europe Sub 1006 G=0.2952 A=0.7048
1000Genomes South Asian Sub 978 G=0.355 A=0.645
1000Genomes American Sub 694 G=0.399 A=0.601
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.2871 A=0.7129
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.3298 A=0.6702
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.3328 A=0.6672
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.4334 A=0.5666, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 G=0.4016 A=0.5984
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 G=0.402 A=0.598
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 G=0.372 A=0.628
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 G=0.300 A=0.700
HGDP-CEPH-db Supplement 1 Europe Sub 320 G=0.316 A=0.684
HGDP-CEPH-db Supplement 1 Africa Sub 242 G=0.669 A=0.331
HGDP-CEPH-db Supplement 1 America Sub 216 G=0.403 A=0.597
HGDP-CEPH-db Supplement 1 Oceania Sub 72 G=0.54 A=0.46
HapMap Global Study-wide 1872 G=0.4760 A=0.5240
HapMap American Sub 756 G=0.380 A=0.620
HapMap African Sub 686 G=0.644 A=0.356
HapMap Asian Sub 254 G=0.465 A=0.535
HapMap Europe Sub 176 G=0.250 A=0.750
Korean Genome Project KOREAN Study-wide 1832 G=0.4088 A=0.5912
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.329 A=0.671
CNV burdens in cranial meningiomas Global Study-wide 784 G=0.389 A=0.611
CNV burdens in cranial meningiomas CRM Sub 784 G=0.389 A=0.611
Northern Sweden ACPOP Study-wide 600 G=0.348 A=0.652
SGDP_PRJ Global Study-wide 428 G=0.271 A=0.729
Qatari Global Study-wide 216 G=0.403 A=0.597
A Vietnamese Genetic Variation Database Global Study-wide 212 G=0.425 A=0.575
Siberian Global Study-wide 46 G=0.28 A=0.72
The Danish reference pan genome Danish Study-wide 40 G=0.30 A=0.70
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 20 G=0.00 A=1.00
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 2 NC_000002.12:g.51725011G>A
GRCh38.p14 chr 2 NC_000002.12:g.51725011G>T
GRCh37.p13 chr 2 NC_000002.11:g.51952149G>A
GRCh37.p13 chr 2 NC_000002.11:g.51952149G>T
Gene: LOC730100, uncharacterized LOC730100 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
NRXN1-DT transcript NR_135237.1:n. N/A Intron 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 T
GRCh38.p14 chr 2 NC_000002.12:g.51725011= NC_000002.12:g.51725011G>A NC_000002.12:g.51725011G>T
GRCh37.p13 chr 2 NC_000002.11:g.51952149= NC_000002.11:g.51952149G>A NC_000002.11:g.51952149G>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#.

101 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss17683255 Feb 27, 2004 (120)
2 CSHL-HAPMAP ss20116041 Feb 27, 2004 (120)
3 BROAD ss28519604 Oct 08, 2004 (124)
4 ABI ss44332609 Mar 13, 2006 (126)
5 ILLUMINA ss66795147 Nov 30, 2006 (127)
6 ILLUMINA ss66922065 Nov 30, 2006 (127)
7 ILLUMINA ss67068718 Nov 30, 2006 (127)
8 ILLUMINA ss70389978 May 17, 2007 (127)
9 ILLUMINA ss70519893 May 26, 2008 (130)
10 ILLUMINA ss71048757 May 17, 2007 (127)
11 ILLUMINA ss75827287 Dec 07, 2007 (129)
12 AFFY ss76704517 Dec 07, 2007 (129)
13 KRIBB_YJKIM ss85072455 Dec 15, 2007 (130)
14 BCMHGSC_JDW ss91160747 Mar 24, 2008 (129)
15 HUMANGENOME_JCVI ss97037943 Feb 06, 2009 (130)
16 1000GENOMES ss109512195 Jan 24, 2009 (130)
17 1000GENOMES ss110264445 Jan 24, 2009 (130)
18 ILLUMINA ss121448265 Dec 01, 2009 (131)
19 ENSEMBL ss132970795 Dec 01, 2009 (131)
20 ENSEMBL ss138443305 Dec 01, 2009 (131)
21 ILLUMINA ss152938720 Dec 01, 2009 (131)
22 GMI ss157059278 Dec 01, 2009 (131)
23 ILLUMINA ss159165527 Dec 01, 2009 (131)
24 COMPLETE_GENOMICS ss163439015 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss164385791 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss166594209 Jul 04, 2010 (132)
27 ILLUMINA ss169794332 Jul 04, 2010 (132)
28 ILLUMINA ss171057635 Jul 04, 2010 (132)
29 BUSHMAN ss200436710 Jul 04, 2010 (132)
30 BCM-HGSC-SUB ss205827940 Jul 04, 2010 (132)
31 1000GENOMES ss219243942 Jul 14, 2010 (132)
32 1000GENOMES ss231167078 Jul 14, 2010 (132)
33 1000GENOMES ss238721502 Jul 15, 2010 (132)
34 BL ss253105826 May 09, 2011 (134)
35 GMI ss276467557 May 04, 2012 (137)
36 GMI ss284345888 Apr 25, 2013 (138)
37 PJP ss292268356 May 09, 2011 (134)
38 ILLUMINA ss536676871 Sep 08, 2015 (146)
39 TISHKOFF ss555562087 Apr 25, 2013 (138)
40 SSMP ss649145513 Apr 25, 2013 (138)
41 ILLUMINA ss825359373 Apr 01, 2015 (144)
42 ILLUMINA ss832678093 Jul 13, 2019 (153)
43 EVA-GONL ss976823338 Aug 21, 2014 (142)
44 JMKIDD_LAB ss1069111103 Aug 21, 2014 (142)
45 1000GENOMES ss1297196544 Aug 21, 2014 (142)
46 DDI ss1428575287 Apr 01, 2015 (144)
47 EVA_GENOME_DK ss1578876184 Apr 01, 2015 (144)
48 EVA_DECODE ss1586234751 Apr 01, 2015 (144)
49 EVA_UK10K_ALSPAC ss1603495318 Apr 01, 2015 (144)
50 EVA_UK10K_TWINSUK ss1646489351 Apr 01, 2015 (144)
51 EVA_SVP ss1712455345 Apr 01, 2015 (144)
52 HAMMER_LAB ss1796746531 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1920057548 Feb 12, 2016 (147)
54 GENOMED ss1968769129 Jul 19, 2016 (147)
55 JJLAB ss2020563027 Sep 14, 2016 (149)
56 USC_VALOUEV ss2148606380 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2230205053 Dec 20, 2016 (150)
58 SYSTEMSBIOZJU ss2624792606 Nov 08, 2017 (151)
59 GRF ss2703172865 Nov 08, 2017 (151)
60 GNOMAD ss2773350311 Nov 08, 2017 (151)
61 SWEGEN ss2989487819 Nov 08, 2017 (151)
62 BIOINF_KMB_FNS_UNIBA ss3024047798 Nov 08, 2017 (151)
63 CSHL ss3344226248 Nov 08, 2017 (151)
64 ILLUMINA ss3628062651 Oct 11, 2018 (152)
65 ILLUMINA ss3638259831 Oct 11, 2018 (152)
66 ILLUMINA ss3639135063 Oct 11, 2018 (152)
67 ILLUMINA ss3639579253 Oct 11, 2018 (152)
68 ILLUMINA ss3643229851 Oct 11, 2018 (152)
69 URBANLAB ss3647033331 Oct 11, 2018 (152)
70 EGCUT_WGS ss3657458528 Jul 13, 2019 (153)
71 EVA_DECODE ss3703870604 Jul 13, 2019 (153)
72 ACPOP ss3728425893 Jul 13, 2019 (153)
73 EVA ss3756748066 Jul 13, 2019 (153)
74 PACBIO ss3783861277 Jul 13, 2019 (153)
75 PACBIO ss3789449322 Jul 13, 2019 (153)
76 PACBIO ss3794322178 Jul 13, 2019 (153)
77 KHV_HUMAN_GENOMES ss3801120105 Jul 13, 2019 (153)
78 EVA ss3826978399 Apr 25, 2020 (154)
79 EVA ss3836898210 Apr 25, 2020 (154)
80 EVA ss3842313652 Apr 25, 2020 (154)
81 HGDP ss3847617620 Apr 25, 2020 (154)
82 SGDP_PRJ ss3852247413 Apr 25, 2020 (154)
83 KRGDB ss3897710605 Apr 25, 2020 (154)
84 KOGIC ss3947731897 Apr 25, 2020 (154)
85 EVA ss3984482441 Apr 26, 2021 (155)
86 EVA ss3984893177 Apr 26, 2021 (155)
87 EVA ss4016995730 Apr 26, 2021 (155)
88 TOPMED ss4505315486 Apr 26, 2021 (155)
89 TOMMO_GENOMICS ss5151310519 Apr 26, 2021 (155)
90 1000G_HIGH_COVERAGE ss5248021642 Oct 12, 2022 (156)
91 EVA ss5328862707 Oct 12, 2022 (156)
92 HUGCELL_USP ss5448231578 Oct 12, 2022 (156)
93 EVA ss5506401981 Oct 12, 2022 (156)
94 1000G_HIGH_COVERAGE ss5523219065 Oct 12, 2022 (156)
95 SANFORD_IMAGENETICS ss5628718962 Oct 12, 2022 (156)
96 TOMMO_GENOMICS ss5679919266 Oct 12, 2022 (156)
97 YY_MCH ss5802194902 Oct 12, 2022 (156)
98 EVA ss5820083190 Oct 12, 2022 (156)
99 EVA ss5852518441 Oct 12, 2022 (156)
100 EVA ss5930320414 Oct 12, 2022 (156)
101 EVA ss5954948024 Oct 12, 2022 (156)
102 1000Genomes NC_000002.11 - 51952149 Oct 11, 2018 (152)
103 1000Genomes_30x NC_000002.12 - 51725011 Oct 12, 2022 (156)
104 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 51952149 Oct 11, 2018 (152)
105 Genetic variation in the Estonian population NC_000002.11 - 51952149 Oct 11, 2018 (152)
106 The Danish reference pan genome NC_000002.11 - 51952149 Apr 25, 2020 (154)
107 gnomAD - Genomes NC_000002.12 - 51725011 Apr 26, 2021 (155)
108 Genome of the Netherlands Release 5 NC_000002.11 - 51952149 Apr 25, 2020 (154)
109 HGDP-CEPH-db Supplement 1 NC_000002.10 - 51805653 Apr 25, 2020 (154)
110 HapMap NC_000002.12 - 51725011 Apr 25, 2020 (154)
111 KOREAN population from KRGDB NC_000002.11 - 51952149 Apr 25, 2020 (154)
112 Korean Genome Project NC_000002.12 - 51725011 Apr 25, 2020 (154)
113 Northern Sweden NC_000002.11 - 51952149 Jul 13, 2019 (153)
114 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000002.11 - 51952149 Apr 26, 2021 (155)
115 CNV burdens in cranial meningiomas NC_000002.11 - 51952149 Apr 26, 2021 (155)
116 Qatari NC_000002.11 - 51952149 Apr 25, 2020 (154)
117 SGDP_PRJ NC_000002.11 - 51952149 Apr 25, 2020 (154)
118 Siberian NC_000002.11 - 51952149 Apr 25, 2020 (154)
119 8.3KJPN NC_000002.11 - 51952149 Apr 26, 2021 (155)
120 14KJPN NC_000002.12 - 51725011 Oct 12, 2022 (156)
121 TopMed NC_000002.12 - 51725011 Apr 26, 2021 (155)
122 UK 10K study - Twins NC_000002.11 - 51952149 Oct 11, 2018 (152)
123 A Vietnamese Genetic Variation Database NC_000002.11 - 51952149 Jul 13, 2019 (153)
124 ALFA NC_000002.12 - 51725011 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)
rs17862761 Dec 02, 2004 (124)
rs60846128 May 26, 2008 (130)
rs386517099 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639135063, ss3639579253 NC_000002.9:51863799:G:A NC_000002.12:51725010:G:A (self)
295512, ss91160747, ss109512195, ss110264445, ss163439015, ss164385791, ss166594209, ss200436710, ss205827940, ss253105826, ss276467557, ss284345888, ss292268356, ss825359373, ss1586234751, ss1712455345, ss3643229851, ss3847617620 NC_000002.10:51805652:G:A NC_000002.12:51725010:G:A (self)
8139541, 4524231, 3196776, 5048748, 1987584, 4887999, 1710758, 119104, 31769, 2099478, 4264393, 1122734, 9279826, 4524231, 982998, ss219243942, ss231167078, ss238721502, ss536676871, ss555562087, ss649145513, ss832678093, ss976823338, ss1069111103, ss1297196544, ss1428575287, ss1578876184, ss1603495318, ss1646489351, ss1796746531, ss1920057548, ss1968769129, ss2020563027, ss2148606380, ss2624792606, ss2703172865, ss2773350311, ss2989487819, ss3344226248, ss3628062651, ss3638259831, ss3657458528, ss3728425893, ss3756748066, ss3783861277, ss3789449322, ss3794322178, ss3826978399, ss3836898210, ss3852247413, ss3897710605, ss3984482441, ss3984893177, ss4016995730, ss5151310519, ss5328862707, ss5506401981, ss5628718962, ss5820083190, ss5954948024 NC_000002.11:51952148:G:A NC_000002.12:51725010:G:A (self)
10745000, 57772759, 1797395, 4109898, 13756370, 309138365, 11606954113, ss2230205053, ss3024047798, ss3647033331, ss3703870604, ss3801120105, ss3842313652, ss3947731897, ss4505315486, ss5248021642, ss5448231578, ss5523219065, ss5679919266, ss5802194902, ss5852518441, ss5930320414 NC_000002.12:51725010:G:A NC_000002.12:51725010:G:A (self)
ss17683255, ss20116041 NT_022184.13:30768080:G:A NC_000002.12:51725010:G:A (self)
ss28519604, ss44332609, ss66795147, ss66922065, ss67068718, ss70389978, ss70519893, ss71048757, ss75827287, ss76704517, ss85072455, ss97037943, ss121448265, ss132970795, ss138443305, ss152938720, ss157059278, ss159165527, ss169794332, ss171057635 NT_022184.15:30774035:G:A NC_000002.12:51725010:G:A (self)
4887999, ss3897710605 NC_000002.11:51952148:G:T NC_000002.12:51725010: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 rs11125375
PMID Title Author Year Journal
19805132 Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. Jiao X et al. 2009 Proceedings of the National Academy of Sciences of the United States of America
22410552 Evaluation of SNPs on chromosome 2p with primary open angle glaucoma in the South Indian cohort. Balasubbu S et al. 2012 Investigative ophthalmology & visual science
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