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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.

rs281865545

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr17:64377836 (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
C>G / C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.469096 (124165/264690, TOPMED)
G=0.1886 (1053/5582, ALFA)
G=0.4498 (851/1892, HapMap) (+ 1 more)
G=0.4236 (776/1832, Korea1K)
Clinical Significance
Reported in ClinVar
Gene : Consequence
PECAM1 : Missense Variant
Publications
7 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 17 NC_000017.11:g.64377836C>G
GRCh38.p13 chr 17 NC_000017.11:g.64377836C>T
GRCh37.p13 chr 17 fix patch HG183_PATCH NW_003315947.1:g.181683C>G
GRCh37.p13 chr 17 fix patch HG183_PATCH NW_003315947.1:g.181683C>T
PECAM1 RefSeqGene NG_047009.1:g.40966G>C
PECAM1 RefSeqGene NG_047009.1:g.40966G>A
Gene: PECAM1, platelet and endothelial cell adhesion molecule 1 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
PECAM1 transcript NM_000442.5:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule precursor NP_000433.4:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript NM_000442.5:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule precursor NP_000433.4:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X4 XM_005276880.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X2 XP_005276937.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X4 XM_005276880.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X2 XP_005276937.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X6 XM_005276881.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X4 XP_005276938.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X6 XM_005276881.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X4 XP_005276938.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X7 XM_005276882.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X5 XP_005276939.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X7 XM_005276882.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X5 XP_005276939.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X1 XM_011524890.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_011523192.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X1 XM_011524890.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_011523192.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X2 XM_011524889.2:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_011523191.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X2 XM_011524889.2:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_011523191.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X3 XM_017024738.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_016880227.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X3 XM_017024738.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X1 XP_016880227.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X5 XM_017024739.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X3 XP_016880228.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X5 XM_017024739.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X3 XP_016880228.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X8 XM_017024740.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X4 XP_016880229.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X8 XM_017024740.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X4 XP_016880229.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X9 XM_005276883.2:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X6 XP_005276940.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X9 XM_005276883.2:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X6 XP_005276940.1:p.Val125Met V (Val) > M (Met) Missense Variant
PECAM1 transcript variant X10 XM_017024741.1:c.373G>C V [GTG] > L [CTG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X7 XP_016880230.1:p.Val125Leu V (Val) > L (Leu) Missense Variant
PECAM1 transcript variant X10 XM_017024741.1:c.373G>A V [GTG] > M [ATG] Coding Sequence Variant
platelet endothelial cell adhesion molecule isoform X7 XP_016880230.1:p.Val125Met V (Val) > M (Met) Missense 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.

Allele: G (allele ID: 166084 )
ClinVar Accession Disease Names Clinical Significance
RCV000014538.2 PLATELET-ENDOTHELIAL CELL ADHESION MOLECULE 1 POLYMORPHISM Benign
RCV000144388.1 not provided Not-Provided
RCV001003440.1 Three Vessel Coronary Disease Benign

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 5582 C=0.8114 G=0.1886, T=0.0000
European Sub 4056 C=0.7515 G=0.2485, T=0.0000
African Sub 1138 C=0.9710 G=0.0290, T=0.0000
African Others Sub 40 C=0.93 G=0.07, T=0.00
African American Sub 1098 C=0.9727 G=0.0273, T=0.0000
Asian Sub 40 C=0.97 G=0.03, T=0.00
East Asian Sub 28 C=1.00 G=0.00, T=0.00
Other Asian Sub 12 C=0.92 G=0.08, T=0.00
Latin American 1 Sub 28 C=1.00 G=0.00, T=0.00
Latin American 2 Sub 138 C=1.000 G=0.000, T=0.000
South Asian Sub 20 C=0.95 G=0.05, T=0.00
Other Sub 162 C=0.938 G=0.062, T=0.000


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 C=0.530904 G=0.469096
HapMap Global Study-wide 1892 C=0.5502 G=0.4498
HapMap American Sub 770 C=0.557 G=0.443
HapMap African Sub 692 C=0.588 G=0.412
HapMap Asian Sub 254 C=0.528 G=0.472
HapMap Europe Sub 176 C=0.403 G=0.597
Korean Genome Project KOREAN Study-wide 1832 C=0.5764 G=0.4236
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 C= G T
GRCh38.p13 chr 17 NC_000017.11:g.64377836= NC_000017.11:g.64377836C>G NC_000017.11:g.64377836C>T
GRCh37.p13 chr 17 fix patch HG183_PATCH NW_003315947.1:g.181683= NW_003315947.1:g.181683C>G NW_003315947.1:g.181683C>T
PECAM1 RefSeqGene NG_047009.1:g.40966= NG_047009.1:g.40966G>C NG_047009.1:g.40966G>A
PECAM1 transcript NM_000442.5:c.373= NM_000442.5:c.373G>C NM_000442.5:c.373G>A
PECAM1 transcript NM_000442.4:c.373= NM_000442.4:c.373G>C NM_000442.4:c.373G>A
PECAM1 transcript variant X2 XM_011524889.2:c.373= XM_011524889.2:c.373G>C XM_011524889.2:c.373G>A
PECAM1 transcript variant X9 XM_005276883.2:c.373= XM_005276883.2:c.373G>C XM_005276883.2:c.373G>A
PECAM1 transcript variant X6 XM_005276883.1:c.373= XM_005276883.1:c.373G>C XM_005276883.1:c.373G>A
PECAM1 transcript variant X4 XM_005276880.1:c.373= XM_005276880.1:c.373G>C XM_005276880.1:c.373G>A
PECAM1 transcript variant X5 XM_017024739.1:c.373= XM_017024739.1:c.373G>C XM_017024739.1:c.373G>A
PECAM1 transcript variant X6 XM_005276881.1:c.373= XM_005276881.1:c.373G>C XM_005276881.1:c.373G>A
PECAM1 transcript variant X7 XM_005276882.1:c.373= XM_005276882.1:c.373G>C XM_005276882.1:c.373G>A
PECAM1 transcript variant X10 XM_017024741.1:c.373= XM_017024741.1:c.373G>C XM_017024741.1:c.373G>A
PECAM1 transcript variant X1 XM_011524890.1:c.373= XM_011524890.1:c.373G>C XM_011524890.1:c.373G>A
PECAM1 transcript variant X8 XM_017024740.1:c.373= XM_017024740.1:c.373G>C XM_017024740.1:c.373G>A
PECAM1 transcript variant X3 XM_017024738.1:c.373= XM_017024738.1:c.373G>C XM_017024738.1:c.373G>A
platelet endothelial cell adhesion molecule precursor NP_000433.4:p.Val125= NP_000433.4:p.Val125Leu NP_000433.4:p.Val125Met
platelet endothelial cell adhesion molecule isoform X1 XP_011523191.1:p.Val125= XP_011523191.1:p.Val125Leu XP_011523191.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X6 XP_005276940.1:p.Val125= XP_005276940.1:p.Val125Leu XP_005276940.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X2 XP_005276937.1:p.Val125= XP_005276937.1:p.Val125Leu XP_005276937.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X3 XP_016880228.1:p.Val125= XP_016880228.1:p.Val125Leu XP_016880228.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X4 XP_005276938.1:p.Val125= XP_005276938.1:p.Val125Leu XP_005276938.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X5 XP_005276939.1:p.Val125= XP_005276939.1:p.Val125Leu XP_005276939.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X7 XP_016880230.1:p.Val125= XP_016880230.1:p.Val125Leu XP_016880230.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X1 XP_011523192.1:p.Val125= XP_011523192.1:p.Val125Leu XP_011523192.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X4 XP_016880229.1:p.Val125= XP_016880229.1:p.Val125Leu XP_016880229.1:p.Val125Met
platelet endothelial cell adhesion molecule isoform X1 XP_016880227.1:p.Val125= XP_016880227.1:p.Val125Leu XP_016880227.1:p.Val125Met
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#.

48 SubSNP, 6 Frequency, 3 ClinVar submissions
No Submitter Submission ID Date (Build)
1 WIAF ss673 Sep 19, 2000 (136)
2 TSC-CSHL ss5451175 Oct 10, 2002 (136)
3 WI_SSAHASNP ss12390818 Apr 01, 2015 (144)
4 IMCJ-GDT ss22888037 Apr 05, 2004 (136)
5 PERLEGEN ss24457615 Sep 20, 2004 (136)
6 ABI ss44000107 Mar 14, 2006 (136)
7 PERLEGEN ss69199836 May 17, 2007 (136)
8 AFFY ss74808080 Aug 16, 2007 (136)
9 AFFY ss76536720 Dec 08, 2007 (136)
10 CGM_KYOTO ss76869594 Dec 06, 2007 (136)
11 SI_EXO ss76894726 Apr 01, 2015 (144)
12 BCMHGSC_JDW ss90635729 Aug 21, 2014 (136)
13 CNG ss95213111 Mar 25, 2008 (136)
14 HUMANGENOME_JCVI ss96553935 Feb 06, 2009 (136)
15 BGI ss103356082 Jul 20, 2010 (136)
16 KRIBB_YJKIM ss104807687 Feb 06, 2009 (136)
17 1000GENOMES ss109859760 Jan 24, 2009 (136)
18 1000GENOMES ss113720642 Jan 25, 2009 (136)
19 ILLUMINA-UK ss118099748 Feb 14, 2009 (136)
20 ENSEMBL ss136530588 Jul 20, 2010 (136)
21 ENSEMBL ss137144930 Jul 20, 2010 (136)
22 GMI ss154535381 Jul 20, 2010 (136)
23 COMPLETE_GENOMICS ss168387992 Jul 20, 2010 (136)
24 ILLUMINA ss169105398 Jul 20, 2010 (136)
25 COMPLETE_GENOMICS ss169992113 Jul 20, 2010 (136)
26 COMPLETE_GENOMICS ss171619188 Jul 20, 2010 (136)
27 BUSHMAN ss202685227 Jul 20, 2010 (136)
28 GMI ss282812778 May 04, 2012 (136)
29 GMI ss287201324 Apr 25, 2013 (136)
30 PJP ss291979400 May 09, 2011 (136)
31 ILLUMINA ss482917321 May 04, 2012 (136)
32 ILLUMINA ss483653033 May 04, 2012 (136)
33 NCBI-CURATED-RECORDS ss537713405 Jan 04, 2013 (137)
34 ILLUMINA ss779493596 Oct 12, 2018 (152)
35 ILLUMINA ss781920641 Mar 15, 2016 (147)
36 ILLUMINA ss834963759 Mar 15, 2016 (147)
37 EVA_SVP ss1713592402 Apr 01, 2015 (144)
38 HUMAN_LONGEVITY ss2218002520 Dec 20, 2016 (150)
39 BIOINF_KMB_FNS_UNIBA ss3028386333 Nov 08, 2017 (151)
40 TOPMED ss3266766201 Nov 08, 2017 (151)
41 TOPMED ss3266766202 Nov 08, 2017 (151)
42 EVA_DECODE ss3700755483 Jul 13, 2019 (153)
43 KHV_HUMAN_GENOMES ss3820101762 Jul 13, 2019 (153)
44 EVA ss3846578376 Apr 27, 2020 (154)
45 KOGIC ss3979133105 Apr 27, 2020 (154)
46 GNOMAD ss4314249696 Apr 26, 2021 (155)
47 GNOMAD ss4314249697 Apr 26, 2021 (155)
48 TOPMED ss5041157095 Apr 26, 2021 (155)
49 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 511604928 (NC_000017.11:64377835:C:G 64150/139766)
Row 511604929 (NC_000017.11:64377835:C:T 1/139864)

- Apr 26, 2021 (155)
50 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 511604928 (NC_000017.11:64377835:C:G 64150/139766)
Row 511604929 (NC_000017.11:64377835:C:T 1/139864)

- Apr 26, 2021 (155)
51 HapMap NC_000017.11 - 64377836 Apr 27, 2020 (154)
52 Korean Genome Project NC_000017.11 - 64377836 Apr 27, 2020 (154)
53 TopMed NC_000017.11 - 64377836 Apr 26, 2021 (155)
54 ALFA NC_000017.11 - 64377836 Apr 26, 2021 (155)
55 ClinVar RCV000014538.2 Oct 12, 2018 (152)
56 ClinVar RCV000144388.1 Oct 12, 2018 (152)
57 ClinVar RCV001003440.1 Apr 27, 2020 (154)
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)
rs668 Aug 25, 2014 (136)
rs1131009 Jan 04, 2002 (102)
rs2228288 Jan 04, 2002 (102)
rs3190515 Oct 08, 2002 (108)
rs4072030 Oct 08, 2004 (123)
rs16947745 Oct 08, 2004 (123)
rs17543802 Oct 08, 2004 (123)
rs28933978 May 26, 2008 (130)
rs41313213 May 26, 2008 (130)
rs52813088 Sep 21, 2007 (128)
rs56552296 May 26, 2008 (130)
rs150163973 Aug 21, 2014 (142)
rs267606942 Aug 24, 2012 (136)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss76536720, ss90635729, ss109859760, ss113720642, ss118099748, ss168387992, ss169992113, ss171619188, ss202685227, ss282812778, ss287201324, ss291979400, ss483653033, ss1713592402 NC_000017.9:59804698:G:G NC_000017.11:64377835:C:G (self)
RCV000014538.2, RCV000144388.1, RCV001003440.1, 1512702, 35511106, 160169505, 256702757, 9121242118, ss537713405, ss2218002520, ss3028386333, ss3266766201, ss3700755483, ss3820101762, ss3846578376, ss3979133105, ss4314249696, ss5041157095 NC_000017.11:64377835:C:G NC_000017.11:64377835:C:G (self)
ss12390818 NT_010783.13:17742898:G:G NC_000017.11:64377835:C:G (self)
ss76894726 NT_010783.14:21102977:G:G NC_000017.11:64377835:C:G (self)
ss673, ss5451175, ss22888037, ss24457615, ss44000107, ss69199836, ss74808080, ss76869594, ss95213111, ss96553935, ss103356082, ss104807687, ss136530588, ss137144930, ss154535381, ss169105398, ss482917321, ss779493596, ss781920641, ss834963759 NW_003315947.1:181682:C:G NC_000017.11:64377835:C:G (self)
9121242118, ss3266766202, ss4314249697 NC_000017.11:64377835:C:T NC_000017.11:64377835:C:T (self)
Help

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

7 citations for rs281865545
PMID Title Author Year Journal
8532023 Polymorphism of adhesion molecule CD31 and its role in acute graft-versus-host disease. Behar E et al. 1996 The New England journal of medicine
21966275 Large-scale gene-centric analysis identifies novel variants for coronary artery disease. IBC 50K CAD Consortium. et al. 2011 PLoS genetics
23316245 The host genetic diversity in malaria infection. de Mendonça VR et al. 2012 Journal of tropical medicine
25201689 PECAM-1 gene polymorphisms and soluble PECAM-1 level in rheumatoid arthritis and systemic lupus erythematosus patients: any link with clinical atherosclerotic events? Pamuk ON et al. 2014 Clinical rheumatology
26662939 Genotype/allelic combinations as potential predictors of myocardial infarction. Nasibullin TR et al. 2016 Molecular biology reports
27335627 Association of PECAM1/CD31 polymorphisms with cerebral malaria. Ohashi J et al. 2016 International journal of molecular epidemiology and genetics
30526437 Diabetes and smoking are more important for prognosis of patients with peripheral arterial disease than some genetic polymorphisms. Boc V et al. 2019 VASA. Zeitschrift fur Gefasskrankheiten
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