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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.

rs45466992

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr11:113397235 (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
A=0.000540 (143/264690, TOPMED)
A=0.000600 (147/245030, GnomAD_exome)
A=0.000727 (138/189854, ALFA) (+ 14 more)
A=0.000556 (78/140242, GnomAD)
A=0.000708 (84/118722, ExAC)
A=0.00028 (22/78696, PAGE_STUDY)
A=0.00047 (6/12672, GO-ESP)
A=0.0003 (2/6404, 1000G_30x)
A=0.0004 (2/5008, 1000G)
A=0.0002 (1/4480, Estonian)
A=0.0008 (3/3854, ALSPAC)
A=0.0008 (3/3708, TWINSUK)
A=0.0024 (8/3296, PRJNA289433)
A=0.001 (1/998, GoNL)
A=0.002 (1/600, NorthernSweden)
A=0.002 (1/534, MGP)
A=0.003 (1/302, FINRISK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ANKK1 : Stop Gained
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 205826 G=0.999271 A=0.000729
European Sub 173370 G=0.999216 A=0.000784
African Sub 9768 G=0.9999 A=0.0001
African Others Sub 360 G=1.000 A=0.000
African American Sub 9408 G=0.9999 A=0.0001
Asian Sub 6348 G=0.9998 A=0.0002
East Asian Sub 4500 G=0.9998 A=0.0002
Other Asian Sub 1848 G=1.0000 A=0.0000
Latin American 1 Sub 442 G=0.998 A=0.002
Latin American 2 Sub 950 G=0.998 A=0.002
South Asian Sub 280 G=1.000 A=0.000
Other Sub 14668 G=0.99939 A=0.00061


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=0.999460 A=0.000540
gnomAD - Exomes Global Study-wide 245030 G=0.999400 A=0.000600
gnomAD - Exomes European Sub 130458 G=0.999080 A=0.000920
gnomAD - Exomes Asian Sub 48546 G=0.99971 A=0.00029
gnomAD - Exomes American Sub 34492 G=0.99974 A=0.00026
gnomAD - Exomes African Sub 15480 G=1.00000 A=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10052 G=0.99990 A=0.00010
gnomAD - Exomes Other Sub 6002 G=0.9995 A=0.0005
Allele Frequency Aggregator Total Global 189854 G=0.999273 A=0.000727
Allele Frequency Aggregator European Sub 163632 G=0.999230 A=0.000770
Allele Frequency Aggregator Other Sub 13268 G=0.99947 A=0.00053
Allele Frequency Aggregator Asian Sub 6348 G=0.9998 A=0.0002
Allele Frequency Aggregator African Sub 4934 G=0.9998 A=0.0002
Allele Frequency Aggregator Latin American 2 Sub 950 G=0.998 A=0.002
Allele Frequency Aggregator Latin American 1 Sub 442 G=0.998 A=0.002
Allele Frequency Aggregator South Asian Sub 280 G=1.000 A=0.000
gnomAD - Genomes Global Study-wide 140242 G=0.999444 A=0.000556
gnomAD - Genomes European Sub 75948 G=0.99916 A=0.00084
gnomAD - Genomes African Sub 42038 G=0.99986 A=0.00014
gnomAD - Genomes American Sub 13656 G=0.99941 A=0.00059
gnomAD - Genomes Ashkenazi Jewish Sub 3322 G=1.0000 A=0.0000
gnomAD - Genomes East Asian Sub 3128 G=1.0000 A=0.0000
gnomAD - Genomes Other Sub 2150 G=1.0000 A=0.0000
ExAC Global Study-wide 118722 G=0.999292 A=0.000708
ExAC Europe Sub 72396 G=0.99898 A=0.00102
ExAC Asian Sub 24438 G=0.99975 A=0.00025
ExAC American Sub 11388 G=0.99974 A=0.00026
ExAC African Sub 9616 G=1.0000 A=0.0000
ExAC Other Sub 884 G=0.999 A=0.001
The PAGE Study Global Study-wide 78696 G=0.99972 A=0.00028
The PAGE Study AfricanAmerican Sub 32514 G=0.99997 A=0.00003
The PAGE Study Mexican Sub 10808 G=0.99954 A=0.00046
The PAGE Study Asian Sub 8318 G=1.0000 A=0.0000
The PAGE Study PuertoRican Sub 7916 G=0.9991 A=0.0009
The PAGE Study NativeHawaiian Sub 4534 G=1.0000 A=0.0000
The PAGE Study Cuban Sub 4230 G=0.9991 A=0.0009
The PAGE Study Dominican Sub 3828 G=0.9995 A=0.0005
The PAGE Study CentralAmerican Sub 2450 G=0.9996 A=0.0004
The PAGE Study SouthAmerican Sub 1982 G=0.9995 A=0.0005
The PAGE Study NativeAmerican Sub 1260 G=0.9992 A=0.0008
The PAGE Study SouthAsian Sub 856 G=1.000 A=0.000
GO Exome Sequencing Project Global Study-wide 12672 G=0.99953 A=0.00047
GO Exome Sequencing Project European American Sub 8438 G=0.9993 A=0.0007
GO Exome Sequencing Project African American Sub 4234 G=1.0000 A=0.0000
1000Genomes_30x Global Study-wide 6404 G=0.9997 A=0.0003
1000Genomes_30x African Sub 1786 G=1.0000 A=0.0000
1000Genomes_30x Europe Sub 1266 G=0.9984 A=0.0016
1000Genomes_30x South Asian Sub 1202 G=1.0000 A=0.0000
1000Genomes_30x East Asian Sub 1170 G=1.0000 A=0.0000
1000Genomes_30x American Sub 980 G=1.000 A=0.000
1000Genomes Global Study-wide 5008 G=0.9996 A=0.0004
1000Genomes African Sub 1322 G=1.0000 A=0.0000
1000Genomes East Asian Sub 1008 G=1.0000 A=0.0000
1000Genomes Europe Sub 1006 G=0.9980 A=0.0020
1000Genomes South Asian Sub 978 G=1.000 A=0.000
1000Genomes American Sub 694 G=1.000 A=0.000
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.9998 A=0.0002
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.9992 A=0.0008
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.9992 A=0.0008
MxGDAR/Encodat-PGx Global Study-wide 3296 G=0.9976 A=0.0024
MxGDAR/Encodat-PGx MxGDAR Sub 3296 G=0.9976 A=0.0024
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.999 A=0.001
Northern Sweden ACPOP Study-wide 600 G=0.998 A=0.002
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.998 A=0.002
FINRISK Finnish from FINRISK project Study-wide 302 G=0.997 A=0.003
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 11 NC_000011.10:g.113397235G>A
GRCh38.p14 chr 11 NC_000011.10:g.113397235G>T
GRCh37.p13 chr 11 NC_000011.9:g.113267957G>A
GRCh37.p13 chr 11 NC_000011.9:g.113267957G>T
ANKK1 RefSeqGene NG_012976.1:g.14445G>A
ANKK1 RefSeqGene NG_012976.1:g.14445G>T
Gene: ANKK1, ankyrin repeat and kinase domain containing 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
ANKK1 transcript NM_178510.2:c.850G>A E [GAG] > K [AAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 NP_848605.1:p.Glu284Lys E (Glu) > K (Lys) Missense Variant
ANKK1 transcript NM_178510.2:c.850G>T E [GAG] > * [TAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 NP_848605.1:p.Glu284Ter E (Glu) > * (Ter) Stop Gained
ANKK1 transcript variant X4 XM_011542738.2:c.658G>A E [GAG] > K [AAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X4 XP_011541040.1:p.Glu220Lys E (Glu) > K (Lys) Missense Variant
ANKK1 transcript variant X4 XM_011542738.2:c.658G>T E [GAG] > * [TAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X4 XP_011541040.1:p.Glu220Ter E (Glu) > * (Ter) Stop Gained
ANKK1 transcript variant X1 XM_011542736.3:c.880G>A E [GAG] > K [AAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X1 XP_011541038.1:p.Glu294Lys E (Glu) > K (Lys) Missense Variant
ANKK1 transcript variant X1 XM_011542736.3:c.880G>T E [GAG] > * [TAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X1 XP_011541038.1:p.Glu294Ter E (Glu) > * (Ter) Stop Gained
ANKK1 transcript variant X2 XM_017017475.2:c.880G>A E [GAG] > K [AAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X2 XP_016872964.1:p.Glu294Lys E (Glu) > K (Lys) Missense Variant
ANKK1 transcript variant X2 XM_017017475.2:c.880G>T E [GAG] > * [TAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X2 XP_016872964.1:p.Glu294Ter E (Glu) > * (Ter) Stop Gained
ANKK1 transcript variant X3 XM_011542737.3:c.850G>A E [GAG] > K [AAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X3 XP_011541039.1:p.Glu284Lys E (Glu) > K (Lys) Missense Variant
ANKK1 transcript variant X3 XM_011542737.3:c.850G>T E [GAG] > * [TAG] Coding Sequence Variant
ankyrin repeat and protein kinase domain-containing protein 1 isoform X3 XP_011541039.1:p.Glu284Ter E (Glu) > * (Ter) Stop Gained
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 11 NC_000011.10:g.113397235= NC_000011.10:g.113397235G>A NC_000011.10:g.113397235G>T
GRCh37.p13 chr 11 NC_000011.9:g.113267957= NC_000011.9:g.113267957G>A NC_000011.9:g.113267957G>T
ANKK1 RefSeqGene NG_012976.1:g.14445= NG_012976.1:g.14445G>A NG_012976.1:g.14445G>T
ANKK1 transcript NM_178510.2:c.850= NM_178510.2:c.850G>A NM_178510.2:c.850G>T
ANKK1 transcript NM_178510.1:c.850= NM_178510.1:c.850G>A NM_178510.1:c.850G>T
ANKK1 transcript variant X1 XM_011542736.3:c.880= XM_011542736.3:c.880G>A XM_011542736.3:c.880G>T
ANKK1 transcript variant X1 XM_011542736.2:c.880= XM_011542736.2:c.880G>A XM_011542736.2:c.880G>T
ANKK1 transcript variant X1 XM_011542736.1:c.880= XM_011542736.1:c.880G>A XM_011542736.1:c.880G>T
ANKK1 transcript variant X3 XM_011542737.3:c.850= XM_011542737.3:c.850G>A XM_011542737.3:c.850G>T
ANKK1 transcript variant X3 XM_011542737.2:c.850= XM_011542737.2:c.850G>A XM_011542737.2:c.850G>T
ANKK1 transcript variant X2 XM_011542737.1:c.850= XM_011542737.1:c.850G>A XM_011542737.1:c.850G>T
ANKK1 transcript variant X4 XM_011542738.2:c.658= XM_011542738.2:c.658G>A XM_011542738.2:c.658G>T
ANKK1 transcript variant X3 XM_011542738.1:c.658= XM_011542738.1:c.658G>A XM_011542738.1:c.658G>T
ANKK1 transcript variant X2 XM_017017475.2:c.880= XM_017017475.2:c.880G>A XM_017017475.2:c.880G>T
ANKK1 transcript variant X2 XM_017017475.1:c.880= XM_017017475.1:c.880G>A XM_017017475.1:c.880G>T
ankyrin repeat and protein kinase domain-containing protein 1 NP_848605.1:p.Glu284= NP_848605.1:p.Glu284Lys NP_848605.1:p.Glu284Ter
ankyrin repeat and protein kinase domain-containing protein 1 isoform X1 XP_011541038.1:p.Glu294= XP_011541038.1:p.Glu294Lys XP_011541038.1:p.Glu294Ter
ankyrin repeat and protein kinase domain-containing protein 1 isoform X3 XP_011541039.1:p.Glu284= XP_011541039.1:p.Glu284Lys XP_011541039.1:p.Glu284Ter
ankyrin repeat and protein kinase domain-containing protein 1 isoform X4 XP_011541040.1:p.Glu220= XP_011541040.1:p.Glu220Lys XP_011541040.1:p.Glu220Ter
ankyrin repeat and protein kinase domain-containing protein 1 isoform X2 XP_016872964.1:p.Glu294= XP_016872964.1:p.Glu294Lys XP_016872964.1:p.Glu294Ter
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#.

50 SubSNP, 17 Frequency submissions
No Submitter Submission ID Date (Build)
1 RSG_JCVI ss69359378 May 16, 2007 (127)
2 1000GENOMES ss488976316 May 04, 2012 (137)
3 EXOME_CHIP ss491459242 May 04, 2012 (137)
4 NHLBI-ESP ss713049454 Apr 25, 2013 (138)
5 ILLUMINA ss783591392 Sep 08, 2015 (146)
6 EVA-GONL ss988978227 Aug 21, 2014 (142)
7 1000GENOMES ss1343024125 Aug 21, 2014 (142)
8 EVA_FINRISK ss1584078059 Apr 01, 2015 (144)
9 EVA_DECODE ss1598644224 Apr 01, 2015 (144)
10 EVA_UK10K_ALSPAC ss1627494106 Apr 01, 2015 (144)
11 EVA_UK10K_TWINSUK ss1670488139 Apr 01, 2015 (144)
12 EVA_EXAC ss1690636642 Apr 01, 2015 (144)
13 EVA_MGP ss1711309084 Apr 01, 2015 (144)
14 ILLUMINA ss1751995098 Sep 08, 2015 (146)
15 ILLUMINA ss1917866564 Feb 12, 2016 (147)
16 ILLUMINA ss1946323019 Feb 12, 2016 (147)
17 ILLUMINA ss1959386517 Feb 12, 2016 (147)
18 JJLAB ss2026913580 Sep 14, 2016 (149)
19 HUMAN_LONGEVITY ss2185828443 Dec 20, 2016 (150)
20 GNOMAD ss2739394473 Nov 08, 2017 (151)
21 GNOMAD ss2748741467 Nov 08, 2017 (151)
22 GNOMAD ss2904623083 Nov 08, 2017 (151)
23 AFFY ss2984957592 Nov 08, 2017 (151)
24 ILLUMINA ss3021377235 Nov 08, 2017 (151)
25 ILLUMINA ss3626753064 Oct 12, 2018 (152)
26 ILLUMINA ss3634475940 Oct 12, 2018 (152)
27 ILLUMINA ss3640183276 Oct 12, 2018 (152)
28 ILLUMINA ss3644575881 Oct 12, 2018 (152)
29 ILLUMINA ss3651744795 Oct 12, 2018 (152)
30 ILLUMINA ss3653729720 Oct 12, 2018 (152)
31 EGCUT_WGS ss3676131017 Jul 13, 2019 (153)
32 EVA_DECODE ss3692627175 Jul 13, 2019 (153)
33 ILLUMINA ss3725277459 Jul 13, 2019 (153)
34 ACPOP ss3738552438 Jul 13, 2019 (153)
35 ILLUMINA ss3744387580 Jul 13, 2019 (153)
36 ILLUMINA ss3744776716 Jul 13, 2019 (153)
37 PAGE_CC ss3771653386 Jul 13, 2019 (153)
38 ILLUMINA ss3772276482 Jul 13, 2019 (153)
39 EVA ss3824672182 Apr 26, 2020 (154)
40 EVA ss3825809571 Apr 26, 2020 (154)
41 EVA ss3984449395 Apr 26, 2021 (155)
42 TOPMED ss4900492310 Apr 26, 2021 (155)
43 1000G_HIGH_COVERAGE ss5288952826 Oct 16, 2022 (156)
44 EVA ss5402336404 Oct 16, 2022 (156)
45 HUGCELL_USP ss5483936787 Oct 16, 2022 (156)
46 1000G_HIGH_COVERAGE ss5585464106 Oct 16, 2022 (156)
47 EVA ss5847648522 Oct 16, 2022 (156)
48 EVA ss5848337375 Oct 16, 2022 (156)
49 EVA ss5921716454 Oct 16, 2022 (156)
50 EVA ss5943431853 Oct 16, 2022 (156)
51 1000Genomes NC_000011.9 - 113267957 Oct 12, 2018 (152)
52 1000Genomes_30x NC_000011.10 - 113397235 Oct 16, 2022 (156)
53 The Avon Longitudinal Study of Parents and Children NC_000011.9 - 113267957 Oct 12, 2018 (152)
54 Genetic variation in the Estonian population NC_000011.9 - 113267957 Oct 12, 2018 (152)
55 ExAC NC_000011.9 - 113267957 Oct 12, 2018 (152)
56 FINRISK NC_000011.9 - 113267957 Apr 26, 2020 (154)
57 gnomAD - Genomes NC_000011.10 - 113397235 Apr 26, 2021 (155)
58 gnomAD - Exomes NC_000011.9 - 113267957 Jul 13, 2019 (153)
59 GO Exome Sequencing Project NC_000011.9 - 113267957 Oct 12, 2018 (152)
60 Genome of the Netherlands Release 5 NC_000011.9 - 113267957 Apr 26, 2020 (154)
61 Medical Genome Project healthy controls from Spanish population NC_000011.9 - 113267957 Apr 26, 2020 (154)
62 Northern Sweden NC_000011.9 - 113267957 Jul 13, 2019 (153)
63 The PAGE Study NC_000011.10 - 113397235 Jul 13, 2019 (153)
64 MxGDAR/Encodat-PGx NC_000011.9 - 113267957 Apr 26, 2021 (155)
65 TopMed NC_000011.10 - 113397235 Apr 26, 2021 (155)
66 UK 10K study - Twins NC_000011.9 - 113267957 Oct 12, 2018 (152)
67 ALFA NC_000011.10 - 113397235 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).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss1598644224 NC_000011.8:112773166:G:A NC_000011.10:113397234:G:A (self)
55608552, 30866568, 21869265, 913001, 74520, 8613232, 1129717, 13774819, 424844, 11837303, 2396, 30866568, ss488976316, ss491459242, ss713049454, ss783591392, ss988978227, ss1343024125, ss1584078059, ss1627494106, ss1670488139, ss1690636642, ss1711309084, ss1751995098, ss1917866564, ss1946323019, ss1959386517, ss2026913580, ss2739394473, ss2748741467, ss2904623083, ss2984957592, ss3021377235, ss3626753064, ss3634475940, ss3640183276, ss3644575881, ss3651744795, ss3653729720, ss3676131017, ss3738552438, ss3744387580, ss3744776716, ss3772276482, ss3824672182, ss3825809571, ss3984449395, ss5402336404, ss5847648522, ss5848337375, ss5943431853 NC_000011.9:113267956:G:A NC_000011.10:113397234:G:A (self)
72990041, 392389226, 874855, 116037966, 3750082900, ss2185828443, ss3692627175, ss3725277459, ss3771653386, ss4900492310, ss5288952826, ss5483936787, ss5585464106, ss5921716454 NC_000011.10:113397234:G:A NC_000011.10:113397234:G:A (self)
ss69359378 NT_033899.8:16830372:G:A NC_000011.10:113397234:G:A (self)
ss2739394473 NC_000011.9:113267956:G:T NC_000011.10:113397234: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 rs45466992

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