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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.

rs488182

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr18:42781646 (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>C / A>G / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.351649 (93078/264690, TOPMED)
A=0.200794 (41178/205076, GENOGRAPHIC)
A=0.335483 (46981/140040, GnomAD) (+ 20 more)
A=0.45661 (12903/28258, 14KJPN)
A=0.28279 (5986/21168, ALFA)
A=0.45692 (7658/16760, 8.3KJPN)
A=0.4285 (2744/6404, 1000G_30x)
A=0.4221 (2114/5008, 1000G)
A=0.2152 (964/4480, Estonian)
A=0.1793 (691/3854, ALSPAC)
A=0.1888 (700/3708, TWINSUK)
A=0.4352 (1275/2930, KOREAN)
A=0.3776 (787/2084, HGDP_Stanford)
A=0.4873 (918/1884, HapMap)
A=0.4514 (827/1832, Korea1K)
A=0.201 (201/998, GoNL)
A=0.197 (118/600, NorthernSweden)
A=0.252 (108/428, SGDP_PRJ)
A=0.231 (50/216, Qatari)
A=0.355 (76/214, Vietnamese)
A=0.25 (12/48, Siberian)
A=0.20 (8/40, GENOME_DK)
A=0.11 (2/18, Ancient Sardinia)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
RIT2 : Intron Variant
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 21168 A=0.28279 G=0.71721, T=0.00000
European Sub 15326 A=0.18531 G=0.81469, T=0.00000
African Sub 3778 A=0.6633 G=0.3367, T=0.0000
African Others Sub 136 A=0.824 G=0.176, T=0.000
African American Sub 3642 A=0.6573 G=0.3427, T=0.0000
Asian Sub 124 A=0.427 G=0.573, T=0.000
East Asian Sub 96 A=0.45 G=0.55, T=0.00
Other Asian Sub 28 A=0.36 G=0.64, T=0.00
Latin American 1 Sub 168 A=0.345 G=0.655, T=0.000
Latin American 2 Sub 670 A=0.327 G=0.673, T=0.000
South Asian Sub 98 A=0.36 G=0.64, T=0.00
Other Sub 1004 A=0.2739 G=0.7261, T=0.0000


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=0.351649 G=0.648351
Genographic Project Global Study-wide 205076 A=0.200794 G=0.799206, T=0.000000
gnomAD - Genomes Global Study-wide 140040 A=0.335483 G=0.664517
gnomAD - Genomes European Sub 75894 A=0.18447 G=0.81553
gnomAD - Genomes African Sub 41928 A=0.63266 G=0.36734
gnomAD - Genomes American Sub 13622 A=0.28799 G=0.71201
gnomAD - Genomes Ashkenazi Jewish Sub 3324 A=0.1363 G=0.8637
gnomAD - Genomes East Asian Sub 3122 A=0.4478 G=0.5522
gnomAD - Genomes Other Sub 2150 A=0.3167 G=0.6833
14KJPN JAPANESE Study-wide 28258 A=0.45661 G=0.54339
Allele Frequency Aggregator Total Global 21168 A=0.28279 G=0.71721, T=0.00000
Allele Frequency Aggregator European Sub 15326 A=0.18531 G=0.81469, T=0.00000
Allele Frequency Aggregator African Sub 3778 A=0.6633 G=0.3367, T=0.0000
Allele Frequency Aggregator Other Sub 1004 A=0.2739 G=0.7261, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 670 A=0.327 G=0.673, T=0.000
Allele Frequency Aggregator Latin American 1 Sub 168 A=0.345 G=0.655, T=0.000
Allele Frequency Aggregator Asian Sub 124 A=0.427 G=0.573, T=0.000
Allele Frequency Aggregator South Asian Sub 98 A=0.36 G=0.64, T=0.00
8.3KJPN JAPANESE Study-wide 16760 A=0.45692 G=0.54308
1000Genomes_30x Global Study-wide 6404 A=0.4285 G=0.5715
1000Genomes_30x African Sub 1786 A=0.7010 G=0.2990
1000Genomes_30x Europe Sub 1266 A=0.1801 G=0.8199
1000Genomes_30x South Asian Sub 1202 A=0.3336 G=0.6664
1000Genomes_30x East Asian Sub 1170 A=0.4427 G=0.5573
1000Genomes_30x American Sub 980 A=0.352 G=0.648
1000Genomes Global Study-wide 5008 A=0.4221 G=0.5779
1000Genomes African Sub 1322 A=0.6989 G=0.3011
1000Genomes East Asian Sub 1008 A=0.4315 G=0.5685
1000Genomes Europe Sub 1006 A=0.1849 G=0.8151
1000Genomes South Asian Sub 978 A=0.337 G=0.663
1000Genomes American Sub 694 A=0.344 G=0.656
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.2152 G=0.7848
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.1793 G=0.8207
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.1888 G=0.8112
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.4352 C=0.0000, G=0.5648, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.3776 G=0.6224
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.468 G=0.532
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.254 G=0.746
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.154 G=0.846
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.153 G=0.847
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.707 G=0.293
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.556 G=0.444
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.94 G=0.06
HapMap Global Study-wide 1884 A=0.4873 G=0.5127
HapMap American Sub 770 A=0.351 G=0.649
HapMap African Sub 688 A=0.728 G=0.272
HapMap Asian Sub 252 A=0.468 G=0.532
HapMap Europe Sub 174 A=0.167 G=0.833
Korean Genome Project KOREAN Study-wide 1832 A=0.4514 G=0.5486
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.201 G=0.799
Northern Sweden ACPOP Study-wide 600 A=0.197 G=0.803
SGDP_PRJ Global Study-wide 428 A=0.252 G=0.748
Qatari Global Study-wide 216 A=0.231 G=0.769
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.355 G=0.645
Siberian Global Study-wide 48 A=0.25 G=0.75
The Danish reference pan genome Danish Study-wide 40 A=0.20 G=0.80
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 18 A=0.11 G=0.89
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 18 NC_000018.10:g.42781646A>C
GRCh38.p14 chr 18 NC_000018.10:g.42781646A>G
GRCh38.p14 chr 18 NC_000018.10:g.42781646A>T
GRCh37.p13 chr 18 NC_000018.9:g.40361611A>C
GRCh37.p13 chr 18 NC_000018.9:g.40361611A>G
GRCh37.p13 chr 18 NC_000018.9:g.40361611A>T
Gene: RIT2, Ras like without CAAX 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
RIT2 transcript variant 2 NM_001272077.2:c.*29-3792…

NM_001272077.2:c.*29-37926T>G

 		N/A Intron Variant
RIT2 transcript variant 1 NM_002930.4:c.427-37926T>G 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 A= C G T
GRCh38.p14 chr 18 NC_000018.10:g.42781646= NC_000018.10:g.42781646A>C NC_000018.10:g.42781646A>G NC_000018.10:g.42781646A>T
GRCh37.p13 chr 18 NC_000018.9:g.40361611= NC_000018.9:g.40361611A>C NC_000018.9:g.40361611A>G NC_000018.9:g.40361611A>T
RIT2 transcript variant 2 NM_001272077.1:c.*29-37926= NM_001272077.1:c.*29-37926T>G NM_001272077.1:c.*29-37926T>C NM_001272077.1:c.*29-37926T>A
RIT2 transcript variant 2 NM_001272077.2:c.*29-37926= NM_001272077.2:c.*29-37926T>G NM_001272077.2:c.*29-37926T>C NM_001272077.2:c.*29-37926T>A
RIT2 transcript variant 1 NM_002930.3:c.427-37926= NM_002930.3:c.427-37926T>G NM_002930.3:c.427-37926T>C NM_002930.3:c.427-37926T>A
RIT2 transcript variant 1 NM_002930.4:c.427-37926= NM_002930.4:c.427-37926T>G NM_002930.4:c.427-37926T>C NM_002930.4:c.427-37926T>A
RIT2 transcript variant X1 XM_005258327.1:c.370-37926= XM_005258327.1:c.370-37926T>G XM_005258327.1:c.370-37926T>C XM_005258327.1:c.370-37926T>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#.

86 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss657877 Aug 11, 2000 (83)
2 SSAHASNP ss21469381 Apr 05, 2004 (121)
3 PERLEGEN ss24031920 Sep 20, 2004 (123)
4 ABI ss44109336 Mar 14, 2006 (126)
5 ILLUMINA ss67765548 Nov 30, 2006 (127)
6 ILLUMINA ss71415814 May 17, 2007 (127)
7 ILLUMINA ss75398353 Dec 06, 2007 (129)
8 BCMHGSC_JDW ss90774508 Mar 24, 2008 (129)
9 HUMANGENOME_JCVI ss96337841 Feb 05, 2009 (130)
10 BGI ss103391342 Dec 01, 2009 (131)
11 1000GENOMES ss110440073 Jan 24, 2009 (130)
12 KRIBB_YJKIM ss119355346 Dec 01, 2009 (131)
13 ENSEMBL ss136426141 Dec 01, 2009 (131)
14 ENSEMBL ss137354138 Dec 01, 2009 (131)
15 GMI ss155096979 Dec 01, 2009 (131)
16 COMPLETE_GENOMICS ss168127430 Jul 04, 2010 (132)
17 COMPLETE_GENOMICS ss171737555 Jul 04, 2010 (132)
18 ILLUMINA ss173857518 Jul 04, 2010 (132)
19 BUSHMAN ss203206389 Jul 04, 2010 (132)
20 BCM-HGSC-SUB ss208220316 Jul 04, 2010 (132)
21 1000GENOMES ss211880784 Jul 14, 2010 (132)
22 1000GENOMES ss227839246 Jul 14, 2010 (132)
23 1000GENOMES ss237450593 Jul 15, 2010 (132)
24 1000GENOMES ss243703225 Jul 15, 2010 (132)
25 BL ss255623224 May 09, 2011 (134)
26 GMI ss282975985 May 04, 2012 (137)
27 GMI ss287276473 Apr 25, 2013 (138)
28 PJP ss292163135 May 09, 2011 (134)
29 ILLUMINA ss537288043 Sep 08, 2015 (146)
30 TISHKOFF ss565618149 Apr 25, 2013 (138)
31 SSMP ss661448112 Apr 25, 2013 (138)
32 EVA-GONL ss993688873 Aug 21, 2014 (142)
33 JMKIDD_LAB ss1081471725 Aug 21, 2014 (142)
34 1000GENOMES ss1360880938 Aug 21, 2014 (142)
35 DDI ss1428204989 Apr 01, 2015 (144)
36 EVA_GENOME_DK ss1578387274 Apr 01, 2015 (144)
37 EVA_UK10K_ALSPAC ss1636793130 Apr 01, 2015 (144)
38 EVA_UK10K_TWINSUK ss1679787163 Apr 01, 2015 (144)
39 EVA_DECODE ss1697745415 Apr 01, 2015 (144)
40 EVA_SVP ss1713623015 Apr 01, 2015 (144)
41 HAMMER_LAB ss1809034951 Sep 08, 2015 (146)
42 WEILL_CORNELL_DGM ss1937157590 Feb 12, 2016 (147)
43 GENOMED ss1968514839 Jul 19, 2016 (147)
44 JJLAB ss2029348055 Sep 14, 2016 (149)
45 USC_VALOUEV ss2157852486 Dec 20, 2016 (150)
46 HUMAN_LONGEVITY ss2221271728 Dec 20, 2016 (150)
47 GRF ss2702438466 Nov 08, 2017 (151)
48 GNOMAD ss2956282954 Nov 08, 2017 (151)
49 SWEGEN ss3016468025 Nov 08, 2017 (151)
50 BIOINF_KMB_FNS_UNIBA ss3028501572 Nov 08, 2017 (151)
51 CSHL ss3352006076 Nov 08, 2017 (151)
52 ILLUMINA ss3627800383 Oct 12, 2018 (152)
53 ILLUMINA ss3638194030 Oct 12, 2018 (152)
54 ILLUMINA ss3643169989 Oct 12, 2018 (152)
55 URBANLAB ss3650782759 Oct 12, 2018 (152)
56 EGCUT_WGS ss3683306585 Jul 13, 2019 (153)
57 EVA_DECODE ss3701587614 Jul 13, 2019 (153)
58 ACPOP ss3742511736 Jul 13, 2019 (153)
59 EVA ss3755342655 Jul 13, 2019 (153)
60 PACBIO ss3788360529 Jul 13, 2019 (153)
61 PACBIO ss3793293042 Jul 13, 2019 (153)
62 PACBIO ss3798179385 Jul 13, 2019 (153)
63 KHV_HUMAN_GENOMES ss3820607776 Jul 13, 2019 (153)
64 EVA ss3835150920 Apr 27, 2020 (154)
65 EVA ss3841192649 Apr 27, 2020 (154)
66 EVA ss3846694647 Apr 27, 2020 (154)
67 HGDP ss3847582031 Apr 27, 2020 (154)
68 SGDP_PRJ ss3886945028 Apr 27, 2020 (154)
69 KRGDB ss3936807059 Apr 27, 2020 (154)
70 KOGIC ss3980081645 Apr 27, 2020 (154)
71 EVA ss3985823510 Apr 26, 2021 (155)
72 TOPMED ss5055427466 Apr 26, 2021 (155)
73 TOMMO_GENOMICS ss5225010020 Apr 26, 2021 (155)
74 1000G_HIGH_COVERAGE ss5305169666 Oct 16, 2022 (156)
75 GENOGRAPHIC ss5314575546 Oct 16, 2022 (156)
76 EVA ss5431191214 Oct 16, 2022 (156)
77 HUGCELL_USP ss5497952964 Oct 16, 2022 (156)
78 EVA ss5511925072 Oct 16, 2022 (156)
79 1000G_HIGH_COVERAGE ss5609946925 Oct 16, 2022 (156)
80 SANFORD_IMAGENETICS ss5661225240 Oct 16, 2022 (156)
81 TOMMO_GENOMICS ss5782755300 Oct 16, 2022 (156)
82 YY_MCH ss5817065408 Oct 16, 2022 (156)
83 EVA ss5827494172 Oct 16, 2022 (156)
84 EVA ss5852037670 Oct 16, 2022 (156)
85 EVA ss5873937375 Oct 16, 2022 (156)
86 EVA ss5952634583 Oct 16, 2022 (156)
87 1000Genomes NC_000018.9 - 40361611 Oct 12, 2018 (152)
88 1000Genomes_30x NC_000018.10 - 42781646 Oct 16, 2022 (156)
89 The Avon Longitudinal Study of Parents and Children NC_000018.9 - 40361611 Oct 12, 2018 (152)
90 Genetic variation in the Estonian population NC_000018.9 - 40361611 Oct 12, 2018 (152)
91 Genographic Project NC_000018.10 - 42781646 Oct 16, 2022 (156)
92 The Danish reference pan genome NC_000018.9 - 40361611 Apr 27, 2020 (154)
93 gnomAD - Genomes NC_000018.10 - 42781646 Apr 26, 2021 (155)
94 Genome of the Netherlands Release 5 NC_000018.9 - 40361611 Apr 27, 2020 (154)
95 HGDP-CEPH-db Supplement 1 NC_000018.8 - 38615609 Apr 27, 2020 (154)
96 HapMap NC_000018.10 - 42781646 Apr 27, 2020 (154)
97 KOREAN population from KRGDB NC_000018.9 - 40361611 Apr 27, 2020 (154)
98 Korean Genome Project NC_000018.10 - 42781646 Apr 27, 2020 (154)
99 Northern Sweden NC_000018.9 - 40361611 Jul 13, 2019 (153)
100 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000018.9 - 40361611 Apr 26, 2021 (155)
101 Qatari NC_000018.9 - 40361611 Apr 27, 2020 (154)
102 SGDP_PRJ NC_000018.9 - 40361611 Apr 27, 2020 (154)
103 Siberian NC_000018.9 - 40361611 Apr 27, 2020 (154)
104 8.3KJPN NC_000018.9 - 40361611 Apr 26, 2021 (155)
105 14KJPN NC_000018.10 - 42781646 Oct 16, 2022 (156)
106 TopMed NC_000018.10 - 42781646 Apr 26, 2021 (155)
107 UK 10K study - Twins NC_000018.9 - 40361611 Oct 12, 2018 (152)
108 A Vietnamese Genetic Variation Database NC_000018.9 - 40361611 Jul 13, 2019 (153)
109 ALFA NC_000018.10 - 42781646 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)
rs16976869 Oct 08, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
43984453, ss3936807059 NC_000018.9:40361610:A:C NC_000018.10:42781645:A:C (self)
259923, ss90774508, ss110440073, ss168127430, ss171737555, ss203206389, ss208220316, ss211880784, ss255623224, ss282975985, ss287276473, ss292163135, ss1697745415, ss1713623015, ss3643169989, ss3847582031 NC_000018.8:38615608:A:G NC_000018.10:42781645:A:G (self)
74205363, 41109194, 29044833, 4579978, 18317261, 43984453, 15796601, 1049437, 19199512, 38962008, 10368840, 82979327, 41109194, 9083534, ss227839246, ss237450593, ss243703225, ss537288043, ss565618149, ss661448112, ss993688873, ss1081471725, ss1360880938, ss1428204989, ss1578387274, ss1636793130, ss1679787163, ss1809034951, ss1937157590, ss1968514839, ss2029348055, ss2157852486, ss2702438466, ss2956282954, ss3016468025, ss3352006076, ss3627800383, ss3638194030, ss3683306585, ss3742511736, ss3755342655, ss3788360529, ss3793293042, ss3798179385, ss3835150920, ss3841192649, ss3886945028, ss3936807059, ss3985823510, ss5225010020, ss5431191214, ss5511925072, ss5661225240, ss5827494172, ss5952634583 NC_000018.9:40361610:A:G NC_000018.10:42781645:A:G (self)
97472860, 121640, 523502632, 1594275, 36459646, 116592404, 270973129, 7661719436, ss2221271728, ss3028501572, ss3650782759, ss3701587614, ss3820607776, ss3846694647, ss3980081645, ss5055427466, ss5305169666, ss5314575546, ss5497952964, ss5609946925, ss5782755300, ss5817065408, ss5852037670, ss5873937375 NC_000018.10:42781645:A:G NC_000018.10:42781645:A:G (self)
ss21469381 NT_010966.13:21850712:A:G NC_000018.10:42781645:A:G (self)
ss657877, ss24031920, ss44109336, ss67765548, ss71415814, ss75398353, ss96337841, ss103391342, ss119355346, ss136426141, ss137354138, ss155096979, ss173857518 NT_010966.14:21850712:A:G NC_000018.10:42781645:A:G (self)
43984453, ss3936807059 NC_000018.9:40361610:A:T NC_000018.10:42781645:A:T (self)
121640, 7661719436, ss5314575546 NC_000018.10:42781645:A:T NC_000018.10:42781645:A: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 rs488182

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