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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.

rs1260333

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:27525757 (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
A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.418629 (110807/264690, TOPMED)
A=0.420844 (55176/131108, GnomAD)
A=0.441553 (49219/111468, ALFA) (+ 16 more)
A=0.38847 (30270/77922, PAGE_STUDY)
G=0.40779 (11449/28076, 14KJPN)
G=0.41522 (6915/16654, 8.3KJPN)
A=0.3752 (2403/6404, 1000G_30x)
A=0.3760 (1883/5008, 1000G)
A=0.4427 (1706/3854, ALSPAC)
A=0.4326 (1604/3708, TWINSUK)
G=0.4665 (1365/2926, KOREAN)
A=0.3974 (810/2038, HGDP_Stanford)
G=0.4368 (795/1820, Korea1K)
A=0.404 (403/998, GoNL)
A=0.468 (380/812, HapMap)
A=0.261 (117/448, SGDP_PRJ)
A=0.431 (93/216, Qatari)
G=0.34 (24/70, Ancient Sardinia)
A=0.30 (15/50, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
8 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 111562 A=0.441736 G=0.558264
European Sub 89156 A=0.46017 G=0.53983
African Sub 8796 A=0.3249 G=0.6751
African Others Sub 308 A=0.315 G=0.685
African American Sub 8488 A=0.3253 G=0.6747
Asian Sub 244 A=0.488 G=0.512
East Asian Sub 170 A=0.482 G=0.518
Other Asian Sub 74 A=0.50 G=0.50
Latin American 1 Sub 568 A=0.437 G=0.563
Latin American 2 Sub 1260 A=0.3817 G=0.6183
South Asian Sub 4960 A=0.3282 G=0.6718
Other Sub 6578 A=0.4439 G=0.5561


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 A=0.418629 G=0.581371
gnomAD - Genomes Global Study-wide 131108 A=0.420844 G=0.579156
gnomAD - Genomes European Sub 71646 A=0.45200 G=0.54800
gnomAD - Genomes African Sub 38578 A=0.33589 G=0.66411
gnomAD - Genomes American Sub 12586 A=0.44589 G=0.55411
gnomAD - Genomes Ashkenazi Jewish Sub 3290 A=0.5626 G=0.4374
gnomAD - Genomes East Asian Sub 2980 A=0.4966 G=0.5034
gnomAD - Genomes Other Sub 2028 A=0.4393 G=0.5607
Allele Frequency Aggregator Total Global 111468 A=0.441553 G=0.558447
Allele Frequency Aggregator European Sub 89080 A=0.46002 G=0.53998
Allele Frequency Aggregator African Sub 8796 A=0.3249 G=0.6751
Allele Frequency Aggregator Other Sub 6560 A=0.4430 G=0.5570
Allele Frequency Aggregator South Asian Sub 4960 A=0.3282 G=0.6718
Allele Frequency Aggregator Latin American 2 Sub 1260 A=0.3817 G=0.6183
Allele Frequency Aggregator Latin American 1 Sub 568 A=0.437 G=0.563
Allele Frequency Aggregator Asian Sub 244 A=0.488 G=0.512
The PAGE Study Global Study-wide 77922 A=0.38847 G=0.61153
The PAGE Study AfricanAmerican Sub 32188 A=0.33690 G=0.66310
The PAGE Study Mexican Sub 10710 A=0.37993 G=0.62007
The PAGE Study Asian Sub 8230 A=0.5418 G=0.4582
The PAGE Study PuertoRican Sub 7844 A=0.4227 G=0.5773
The PAGE Study NativeHawaiian Sub 4492 A=0.3720 G=0.6280
The PAGE Study Cuban Sub 4194 A=0.4771 G=0.5229
The PAGE Study Dominican Sub 3780 A=0.4124 G=0.5876
The PAGE Study CentralAmerican Sub 2422 A=0.3646 G=0.6354
The PAGE Study SouthAmerican Sub 1966 A=0.3820 G=0.6180
The PAGE Study NativeAmerican Sub 1248 A=0.3758 G=0.6242
The PAGE Study SouthAsian Sub 848 A=0.292 G=0.708
14KJPN JAPANESE Study-wide 28076 A=0.59221 G=0.40779
8.3KJPN JAPANESE Study-wide 16654 A=0.58478 G=0.41522
1000Genomes_30x Global Study-wide 6404 A=0.3752 G=0.6248
1000Genomes_30x African Sub 1786 A=0.3141 G=0.6859
1000Genomes_30x Europe Sub 1266 A=0.4597 G=0.5403
1000Genomes_30x South Asian Sub 1202 A=0.2612 G=0.7388
1000Genomes_30x East Asian Sub 1170 A=0.4803 G=0.5197
1000Genomes_30x American Sub 980 A=0.392 G=0.608
1000Genomes Global Study-wide 5008 A=0.3760 G=0.6240
1000Genomes African Sub 1322 A=0.3132 G=0.6868
1000Genomes East Asian Sub 1008 A=0.4802 G=0.5198
1000Genomes Europe Sub 1006 A=0.4493 G=0.5507
1000Genomes South Asian Sub 978 A=0.259 G=0.741
1000Genomes American Sub 694 A=0.403 G=0.597
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.4427 G=0.5573
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.4326 G=0.5674
KOREAN population from KRGDB KOREAN Study-wide 2926 A=0.5335 G=0.4665
HGDP-CEPH-db Supplement 1 Global Study-wide 2038 A=0.3974 G=0.6026
HGDP-CEPH-db Supplement 1 Est_Asia Sub 452 A=0.458 G=0.542
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 402 A=0.378 G=0.622
HGDP-CEPH-db Supplement 1 Middle_Est Sub 348 A=0.580 G=0.420
HGDP-CEPH-db Supplement 1 Europe Sub 310 A=0.490 G=0.510
HGDP-CEPH-db Supplement 1 Africa Sub 240 A=0.242 G=0.758
HGDP-CEPH-db Supplement 1 America Sub 214 A=0.173 G=0.827
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.03 G=0.97
Korean Genome Project KOREAN Study-wide 1820 A=0.5632 G=0.4368
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.404 G=0.596
HapMap Global Study-wide 812 A=0.468 G=0.532
HapMap American Sub 286 A=0.329 G=0.671
HapMap Asian Sub 244 A=0.619 G=0.381
HapMap Europe Sub 170 A=0.565 G=0.435
HapMap African Sub 112 A=0.348 G=0.652
SGDP_PRJ Global Study-wide 448 A=0.261 G=0.739
Qatari Global Study-wide 216 A=0.431 G=0.569
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 70 A=0.66 G=0.34
Siberian Global Study-wide 50 A=0.30 G=0.70
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.27525757A>G
GRCh37.p13 chr 2 NC_000002.11:g.27748624A>G
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 A= G
GRCh38.p14 chr 2 NC_000002.12:g.27525757= NC_000002.12:g.27525757A>G
GRCh37.p13 chr 2 NC_000002.11:g.27748624= NC_000002.11:g.27748624A>G
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#.

100 SubSNP, 19 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss1932527 Oct 18, 2000 (87)
2 SC_JCM ss2446324 Nov 09, 2000 (123)
3 WI_SSAHASNP ss6424384 Feb 20, 2003 (123)
4 SC_SNP ss15841293 Feb 27, 2004 (123)
5 ILLUMINA ss66798182 Nov 30, 2006 (127)
6 ILLUMINA ss70413027 May 17, 2007 (127)
7 ILLUMINA ss70577095 May 24, 2008 (130)
8 ILLUMINA ss71118723 May 17, 2007 (127)
9 ILLUMINA ss75851357 Dec 06, 2007 (129)
10 1000GENOMES ss109344810 Jan 24, 2009 (130)
11 ILLUMINA ss121584086 Dec 01, 2009 (131)
12 ILLUMINA ss153244279 Dec 01, 2009 (131)
13 ILLUMINA ss159226568 Dec 01, 2009 (131)
14 ILLUMINA ss160286617 Dec 01, 2009 (131)
15 COMPLETE_GENOMICS ss163221836 Jul 04, 2010 (132)
16 COMPLETE_GENOMICS ss164049971 Jul 04, 2010 (132)
17 ILLUMINA ss170178036 Jul 04, 2010 (132)
18 ILLUMINA ss172179756 Jul 04, 2010 (132)
19 BUSHMAN ss200192922 Jul 04, 2010 (132)
20 BCM-HGSC-SUB ss205782667 Jul 04, 2010 (132)
21 1000GENOMES ss210849975 Jul 14, 2010 (132)
22 1000GENOMES ss219134041 Jul 14, 2010 (132)
23 1000GENOMES ss231086345 Jul 14, 2010 (132)
24 1000GENOMES ss238660117 Jul 15, 2010 (132)
25 BL ss252989649 May 09, 2011 (134)
26 GMI ss276395003 May 04, 2012 (137)
27 GMI ss284312656 Apr 25, 2013 (138)
28 ILLUMINA ss410833706 Sep 17, 2011 (135)
29 ILLUMINA ss480363258 Sep 08, 2015 (146)
30 EXOME_CHIP ss491316771 May 04, 2012 (137)
31 SSMP ss649013462 Apr 25, 2013 (138)
32 ILLUMINA ss783354824 Sep 08, 2015 (146)
33 ILLUMINA ss825382301 Apr 01, 2015 (144)
34 ILLUMINA ss832738933 Jul 13, 2019 (153)
35 EVA-GONL ss976615308 Aug 21, 2014 (142)
36 JMKIDD_LAB ss1068952999 Aug 21, 2014 (142)
37 1000GENOMES ss1296399006 Aug 21, 2014 (142)
38 DDI ss1428514635 Apr 01, 2015 (144)
39 EVA_UK10K_ALSPAC ss1603069647 Apr 01, 2015 (144)
40 EVA_UK10K_TWINSUK ss1646063680 Apr 01, 2015 (144)
41 EVA_SVP ss1712440211 Apr 01, 2015 (144)
42 ILLUMINA ss1752350638 Sep 08, 2015 (146)
43 HAMMER_LAB ss1796455100 Sep 08, 2015 (146)
44 ILLUMINA ss1917747325 Feb 12, 2016 (147)
45 WEILL_CORNELL_DGM ss1919847493 Feb 12, 2016 (147)
46 ILLUMINA ss1946035464 Feb 12, 2016 (147)
47 ILLUMINA ss1958400232 Feb 12, 2016 (147)
48 GENOMED ss1968722019 Jul 19, 2016 (147)
49 USC_VALOUEV ss2148496718 Dec 20, 2016 (150)
50 SYSTEMSBIOZJU ss2624741572 Nov 08, 2017 (151)
51 ILLUMINA ss2633587607 Nov 08, 2017 (151)
52 GRF ss2703057774 Nov 08, 2017 (151)
53 GNOMAD ss2771108076 Nov 08, 2017 (151)
54 AFFY ss2985162620 Nov 08, 2017 (151)
55 AFFY ss2985786864 Nov 08, 2017 (151)
56 SWEGEN ss2989173856 Nov 08, 2017 (151)
57 ILLUMINA ss3021952604 Nov 08, 2017 (151)
58 CSHL ss3344130440 Nov 08, 2017 (151)
59 ILLUMINA ss3628018961 Oct 11, 2018 (152)
60 ILLUMINA ss3634756914 Oct 11, 2018 (152)
61 ILLUMINA ss3636442749 Oct 11, 2018 (152)
62 ILLUMINA ss3638248947 Oct 11, 2018 (152)
63 ILLUMINA ss3639576040 Oct 11, 2018 (152)
64 ILLUMINA ss3640464218 Oct 11, 2018 (152)
65 ILLUMINA ss3643219926 Oct 11, 2018 (152)
66 ILLUMINA ss3644738160 Oct 11, 2018 (152)
67 ILLUMINA ss3652381947 Oct 11, 2018 (152)
68 ILLUMINA ss3653933348 Oct 11, 2018 (152)
69 EVA_DECODE ss3703490826 Jul 13, 2019 (153)
70 ILLUMINA ss3744473070 Jul 13, 2019 (153)
71 ILLUMINA ss3745056865 Jul 13, 2019 (153)
72 EVA ss3756504639 Jul 13, 2019 (153)
73 PAGE_CC ss3770905160 Jul 13, 2019 (153)
74 ILLUMINA ss3772553744 Jul 13, 2019 (153)
75 KHV_HUMAN_GENOMES ss3800885190 Jul 13, 2019 (153)
76 EVA ss3826880757 Apr 25, 2020 (154)
77 EVA ss3836847597 Apr 25, 2020 (154)
78 EVA ss3842262191 Apr 25, 2020 (154)
79 HGDP ss3847610601 Apr 25, 2020 (154)
80 SGDP_PRJ ss3851844867 Apr 25, 2020 (154)
81 KRGDB ss3897258607 Apr 25, 2020 (154)
82 KOGIC ss3947356283 Apr 25, 2020 (154)
83 EVA ss3984880690 Apr 26, 2021 (155)
84 EVA ss4016985825 Apr 26, 2021 (155)
85 TOPMED ss4498398947 Apr 26, 2021 (155)
86 TOMMO_GENOMICS ss5150422597 Apr 26, 2021 (155)
87 1000G_HIGH_COVERAGE ss5247340743 Oct 17, 2022 (156)
88 EVA ss5327599064 Oct 17, 2022 (156)
89 HUGCELL_USP ss5447609988 Oct 17, 2022 (156)
90 1000G_HIGH_COVERAGE ss5522181597 Oct 17, 2022 (156)
91 SANFORD_IMAGENETICS ss5628334094 Oct 17, 2022 (156)
92 TOMMO_GENOMICS ss5678775228 Oct 17, 2022 (156)
93 YY_MCH ss5802029461 Oct 17, 2022 (156)
94 EVA ss5819820377 Oct 17, 2022 (156)
95 EVA ss5847184074 Oct 17, 2022 (156)
96 EVA ss5847860712 Oct 17, 2022 (156)
97 EVA ss5852439891 Oct 17, 2022 (156)
98 EVA ss5929522210 Oct 17, 2022 (156)
99 EVA ss5954536286 Oct 17, 2022 (156)
100 EVA ss5979560324 Oct 17, 2022 (156)
101 1000Genomes NC_000002.11 - 27748624 Oct 11, 2018 (152)
102 1000Genomes_30x NC_000002.12 - 27525757 Oct 17, 2022 (156)
103 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 27748624 Oct 11, 2018 (152)
104 gnomAD - Genomes NC_000002.12 - 27525757 Apr 26, 2021 (155)
105 Genome of the Netherlands Release 5 NC_000002.11 - 27748624 Apr 25, 2020 (154)
106 HGDP-CEPH-db Supplement 1 NC_000002.10 - 27602128 Apr 25, 2020 (154)
107 HapMap NC_000002.12 - 27525757 Apr 25, 2020 (154)
108 KOREAN population from KRGDB NC_000002.11 - 27748624 Apr 25, 2020 (154)
109 Korean Genome Project NC_000002.12 - 27525757 Apr 25, 2020 (154)
110 The PAGE Study NC_000002.12 - 27525757 Jul 13, 2019 (153)
111 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000002.11 - 27748624 Apr 26, 2021 (155)
112 Qatari NC_000002.11 - 27748624 Apr 25, 2020 (154)
113 SGDP_PRJ NC_000002.11 - 27748624 Apr 25, 2020 (154)
114 Siberian NC_000002.11 - 27748624 Apr 25, 2020 (154)
115 8.3KJPN NC_000002.11 - 27748624 Apr 26, 2021 (155)
116 14KJPN NC_000002.12 - 27525757 Oct 17, 2022 (156)
117 TopMed NC_000002.12 - 27525757 Apr 26, 2021 (155)
118 UK 10K study - Twins NC_000002.11 - 27748624 Oct 11, 2018 (152)
119 ALFA NC_000002.12 - 27525757 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)
rs1628913 Sep 24, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639576040 NC_000002.9:27660274:A:G NC_000002.12:27525756:A:G (self)
288493, ss109344810, ss163221836, ss164049971, ss200192922, ss205782667, ss210849975, ss252989649, ss276395003, ss284312656, ss825382301, ss1712440211, ss3643219926, ss3847610601 NC_000002.10:27602127:A:G NC_000002.12:27525756:A:G (self)
7317465, 4061769, 1784513, 4436001, 106617, 1889423, 3861847, 1013072, 8391904, 4061769, ss219134041, ss231086345, ss238660117, ss480363258, ss491316771, ss649013462, ss783354824, ss832738933, ss976615308, ss1068952999, ss1296399006, ss1428514635, ss1603069647, ss1646063680, ss1752350638, ss1796455100, ss1917747325, ss1919847493, ss1946035464, ss1958400232, ss1968722019, ss2148496718, ss2624741572, ss2633587607, ss2703057774, ss2771108076, ss2985162620, ss2985786864, ss2989173856, ss3021952604, ss3344130440, ss3628018961, ss3634756914, ss3636442749, ss3638248947, ss3640464218, ss3644738160, ss3652381947, ss3653933348, ss3744473070, ss3745056865, ss3756504639, ss3772553744, ss3826880757, ss3836847597, ss3851844867, ss3897258607, ss3984880690, ss4016985825, ss5150422597, ss5327599064, ss5628334094, ss5819820377, ss5847184074, ss5847860712, ss5954536286, ss5979560324 NC_000002.11:27748623:A:G NC_000002.12:27525756:A:G (self)
9707532, 51996383, 1758657, 3734284, 126629, 12612332, 302221826, 15171346385, ss3703490826, ss3770905160, ss3800885190, ss3842262191, ss3947356283, ss4498398947, ss5247340743, ss5447609988, ss5522181597, ss5678775228, ss5802029461, ss5852439891, ss5929522210 NC_000002.12:27525756:A:G NC_000002.12:27525756:A:G (self)
ss15841293 NT_022184.13:6564556:A:G NC_000002.12:27525756:A:G (self)
ss1932527, ss2446324, ss6424384, ss66798182, ss70413027, ss70577095, ss71118723, ss75851357, ss121584086, ss153244279, ss159226568, ss160286617, ss170178036, ss172179756, ss410833706 NT_022184.15:6570510:A:G NC_000002.12:27525756:A:G (self)
Help

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

8 citations for rs1260333
PMID Title Author Year Journal
18439548 Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. Ridker PM et al. 2008 American journal of human genetics
18439552 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. Reiner AP et al. 2008 American journal of human genetics
20864672 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Waterworth DM et al. 2010 Arteriosclerosis, thrombosis, and vascular biology
23832694 Common genetic variants associated with lipid profiles in a Chinese pediatric population. Shen Y et al. 2013 Human genetics
24763700 New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. Vinayagamoorthy N et al. 2014 PloS one
29531563 Lipid regulatory genes polymorphism in children with and without obesity and cardiometabolic risk factors: The CASPIAN-III study. Hovsepian S et al. 2018 Journal of research in medical sciences
29858861 Relationship of lipid regulatory gene polymorphisms and dyslipidemia in a pediatric population: the CASPIAN III study. Hovsepian S et al. 2018 Hormones (Athens, Greece)
31910446 Genome-wide association study of metabolic syndrome in Korean populations. Oh SW et al. 2020 PloS one
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