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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.

rs2904596

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr6:31493374 (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
T>C / T>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.233500 (61805/264690, TOPMED)
G=0.225462 (31598/140148, GnomAD)
G=0.19870 (5615/28258, 14KJPN) (+ 15 more)
G=0.23954 (4525/18890, ALFA)
G=0.19779 (3315/16760, 8.3KJPN)
G=0.2270 (1454/6404, 1000G_30x)
G=0.2302 (1153/5008, 1000G)
G=0.2916 (1124/3854, ALSPAC)
G=0.2689 (997/3708, TWINSUK)
G=0.2488 (729/2930, KOREAN)
G=0.224 (224/998, GoNL)
G=0.270 (162/600, NorthernSweden)
T=0.406 (91/224, SGDP_PRJ)
G=0.157 (34/216, Qatari)
G=0.093 (20/214, Vietnamese)
G=0.192 (20/104, HapMap)
G=0.28 (11/40, GENOME_DK)
T=0.39 (11/28, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
MICB-DT : Intron Variant
MICB : 2KB Upstream 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 18890 T=0.76046 G=0.23954
European Sub 14286 T=0.74507 G=0.25493
African Sub 2946 T=0.8411 G=0.1589
African Others Sub 114 T=0.816 G=0.184
African American Sub 2832 T=0.8422 G=0.1578
Asian Sub 112 T=0.821 G=0.179
East Asian Sub 86 T=0.81 G=0.19
Other Asian Sub 26 T=0.85 G=0.15
Latin American 1 Sub 146 T=0.815 G=0.185
Latin American 2 Sub 610 T=0.689 G=0.311
South Asian Sub 98 T=0.76 G=0.24
Other Sub 692 T=0.777 G=0.223


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 T=0.766500 G=0.233500
gnomAD - Genomes Global Study-wide 140148 T=0.774538 G=0.225462
gnomAD - Genomes European Sub 75880 T=0.74653 G=0.25347
gnomAD - Genomes African Sub 42006 T=0.83700 G=0.16300
gnomAD - Genomes American Sub 13662 T=0.72069 G=0.27931
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.7912 G=0.2088
gnomAD - Genomes East Asian Sub 3128 T=0.8219 G=0.1781
gnomAD - Genomes Other Sub 2148 T=0.7900 G=0.2100
14KJPN JAPANESE Study-wide 28258 T=0.80130 G=0.19870
Allele Frequency Aggregator Total Global 18890 T=0.76046 G=0.23954
Allele Frequency Aggregator European Sub 14286 T=0.74507 G=0.25493
Allele Frequency Aggregator African Sub 2946 T=0.8411 G=0.1589
Allele Frequency Aggregator Other Sub 692 T=0.777 G=0.223
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.689 G=0.311
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.815 G=0.185
Allele Frequency Aggregator Asian Sub 112 T=0.821 G=0.179
Allele Frequency Aggregator South Asian Sub 98 T=0.76 G=0.24
8.3KJPN JAPANESE Study-wide 16760 T=0.80221 G=0.19779
1000Genomes_30x Global Study-wide 6404 T=0.7730 G=0.2270
1000Genomes_30x African Sub 1786 T=0.8410 G=0.1590
1000Genomes_30x Europe Sub 1266 T=0.7006 G=0.2994
1000Genomes_30x South Asian Sub 1202 T=0.7504 G=0.2496
1000Genomes_30x East Asian Sub 1170 T=0.8385 G=0.1615
1000Genomes_30x American Sub 980 T=0.692 G=0.308
1000Genomes Global Study-wide 5008 T=0.7698 G=0.2302
1000Genomes African Sub 1322 T=0.8434 G=0.1566
1000Genomes East Asian Sub 1008 T=0.8343 G=0.1657
1000Genomes Europe Sub 1006 T=0.6918 G=0.3082
1000Genomes South Asian Sub 978 T=0.744 G=0.256
1000Genomes American Sub 694 T=0.684 G=0.316
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.7084 G=0.2916
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.7311 G=0.2689
KOREAN population from KRGDB KOREAN Study-wide 2930 T=0.7512 C=0.0000, G=0.2488
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.776 G=0.224
Northern Sweden ACPOP Study-wide 600 T=0.730 G=0.270
SGDP_PRJ Global Study-wide 224 T=0.406 G=0.594
Qatari Global Study-wide 216 T=0.843 G=0.157
A Vietnamese Genetic Variation Database Global Study-wide 214 T=0.907 G=0.093
HapMap Global Study-wide 104 T=0.808 G=0.192
HapMap African Sub 104 T=0.808 G=0.192
The Danish reference pan genome Danish Study-wide 40 T=0.72 G=0.28
Siberian Global Study-wide 28 T=0.39 G=0.61
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 6 NC_000006.12:g.31493374T>C
GRCh38.p14 chr 6 NC_000006.12:g.31493374T>G
GRCh37.p13 chr 6 NC_000006.11:g.31461151T>C
GRCh37.p13 chr 6 NC_000006.11:g.31461151T>G
MICB RefSeqGene NG_021405.1:g.297T>C
MICB RefSeqGene NG_021405.1:g.297T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.2970715T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.2970715T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.2970821T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.2970821T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.2825942T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.2825942T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.2775858T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.2775858T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.2792651T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.2792651T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.2791949T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.2791949T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.2835329T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.2835329T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.2840914T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.2840914T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.2740982G>T
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.2740982G>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.2746567G>T
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.2746567G>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.2749255T>C
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.2749255T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.2754851T>C
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.2754851T>G
Gene: MICB, MHC class I polypeptide-related sequence B (plus strand) : 2KB Upstream Variant
Molecule type Change Amino acid[Codon] SO Term
MICB transcript variant 2 NM_001289160.2:c. N/A Upstream Transcript Variant
MICB transcript variant 3 NM_001289161.2:c. N/A N/A
MICB transcript variant 1 NM_005931.5:c. N/A N/A
Gene: MICB-DT, MICB divergent transcript (minus strand)
Molecule type Change Amino acid[Codon] SO Term
MICB-DT transcript NR_149132.1: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 T= C G
GRCh38.p14 chr 6 NC_000006.12:g.31493374= NC_000006.12:g.31493374T>C NC_000006.12:g.31493374T>G
GRCh37.p13 chr 6 NC_000006.11:g.31461151= NC_000006.11:g.31461151T>C NC_000006.11:g.31461151T>G
MICB RefSeqGene NG_021405.1:g.297= NG_021405.1:g.297T>C NG_021405.1:g.297T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.3:g.2970715= NT_113891.3:g.2970715T>C NT_113891.3:g.2970715T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_COX_CTG1 NT_113891.2:g.2970821= NT_113891.2:g.2970821T>C NT_113891.2:g.2970821T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.2:g.2825942= NT_167244.2:g.2825942T>C NT_167244.2:g.2825942T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_APD_CTG1 NT_167244.1:g.2775858= NT_167244.1:g.2775858T>C NT_167244.1:g.2775858T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.2:g.2792651= NT_167249.2:g.2792651T>C NT_167249.2:g.2792651T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_SSTO_CTG1 NT_167249.1:g.2791949= NT_167249.1:g.2791949T>C NT_167249.1:g.2791949T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.2:g.2835329= NT_167247.2:g.2835329T>C NT_167247.2:g.2835329T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_MCF_CTG1 NT_167247.1:g.2840914= NT_167247.1:g.2840914T>C NT_167247.1:g.2840914T>G
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.2:g.2740982G>T NT_167245.2:g.2740982G>C NT_167245.2:g.2740982=
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_DBB_CTG1 NT_167245.1:g.2746567G>T NT_167245.1:g.2746567G>C NT_167245.1:g.2746567=
GRCh38.p14 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.2:g.2749255= NT_167248.2:g.2749255T>C NT_167248.2:g.2749255T>G
GRCh37.p13 chr 6 alt locus HSCHR6_MHC_QBL_CTG1 NT_167248.1:g.2754851= NT_167248.1:g.2754851T>C NT_167248.1:g.2754851T>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#.

59 SubSNP, 18 Frequency submissions
No Submitter Submission ID Date (Build)
1 SC_JCM ss4099281 Nov 05, 2001 (101)
2 ABI ss42659282 Mar 14, 2006 (126)
3 SI_MHC_SNP ss52085710 Oct 14, 2006 (127)
4 1000GENOMES ss114143469 Feb 14, 2009 (131)
5 ILLUMINA ss160597654 Dec 01, 2009 (131)
6 COMPLETE_GENOMICS ss163347057 Jul 04, 2010 (132)
7 BCM-HGSC-SUB ss207414973 Jul 04, 2010 (132)
8 1000GENOMES ss222303739 Jul 14, 2010 (132)
9 1000GENOMES ss233398760 Jul 14, 2010 (132)
10 1000GENOMES ss240469503 Jul 15, 2010 (132)
11 ILLUMINA ss244292875 Jul 04, 2010 (132)
12 GMI ss278726521 May 04, 2012 (137)
13 PJP ss293825679 May 09, 2011 (137)
14 ILLUMINA ss481605022 Sep 08, 2015 (146)
15 TISHKOFF ss559113743 Apr 25, 2013 (138)
16 SSMP ss653034885 Apr 25, 2013 (138)
17 EVA-GONL ss982765407 Aug 21, 2014 (142)
18 JMKIDD_LAB ss1073505388 Aug 21, 2014 (142)
19 1000GENOMES ss1319556574 Aug 21, 2014 (142)
20 EVA_GENOME_DK ss1581606321 Apr 01, 2015 (144)
21 EVA_DECODE ss1592309332 Apr 01, 2015 (144)
22 EVA_UK10K_ALSPAC ss1615276553 Apr 01, 2015 (144)
23 EVA_UK10K_TWINSUK ss1658270586 Apr 01, 2015 (144)
24 HAMMER_LAB ss1804357840 Sep 08, 2015 (146)
25 WEILL_CORNELL_DGM ss1926017850 Feb 12, 2016 (147)
26 GENOMED ss1970357272 Jul 19, 2016 (147)
27 JJLAB ss2023641903 Sep 14, 2016 (149)
28 USC_VALOUEV ss2151808262 Dec 20, 2016 (150)
29 SYSTEMSBIOZJU ss2626308256 Nov 08, 2017 (151)
30 GRF ss2707402035 Nov 08, 2017 (151)
31 SWEGEN ss2998795089 Nov 08, 2017 (151)
32 BIOINF_KMB_FNS_UNIBA ss3025608046 Nov 08, 2017 (151)
33 ILLUMINA ss3636778020 Oct 12, 2018 (152)
34 URBANLAB ss3648309830 Oct 12, 2018 (152)
35 EVA_DECODE ss3716907673 Jul 13, 2019 (153)
36 ACPOP ss3733361149 Jul 13, 2019 (153)
37 EVA ss3764821870 Jul 13, 2019 (153)
38 KHV_HUMAN_GENOMES ss3807977261 Jul 13, 2019 (153)
39 EVA ss3829832416 Apr 26, 2020 (154)
40 EVA ss3838394448 Apr 26, 2020 (154)
41 EVA ss3843836623 Apr 26, 2020 (154)
42 SGDP_PRJ ss3864254095 Apr 26, 2020 (154)
43 KRGDB ss3911028799 Apr 26, 2020 (154)
44 VINODS ss4025188429 Apr 26, 2021 (155)
45 VINODS ss4025247853 Apr 26, 2021 (155)
46 VINODS ss4025287428 Apr 26, 2021 (155)
47 TOPMED ss4698377211 Apr 26, 2021 (155)
48 TOMMO_GENOMICS ss5176835176 Apr 26, 2021 (155)
49 1000G_HIGH_COVERAGE ss5267935349 Oct 17, 2022 (156)
50 HUGCELL_USP ss5465669623 Oct 17, 2022 (156)
51 EVA ss5508427959 Oct 17, 2022 (156)
52 1000G_HIGH_COVERAGE ss5553591087 Oct 17, 2022 (156)
53 SANFORD_IMAGENETICS ss5640088753 Oct 17, 2022 (156)
54 TOMMO_GENOMICS ss5714689470 Oct 17, 2022 (156)
55 YY_MCH ss5807306992 Oct 17, 2022 (156)
56 EVA ss5842026230 Oct 17, 2022 (156)
57 EVA ss5855283599 Oct 17, 2022 (156)
58 EVA ss5883242533 Oct 17, 2022 (156)
59 EVA ss5968590565 Oct 17, 2022 (156)
60 1000Genomes NC_000006.11 - 31461151 Oct 12, 2018 (152)
61 1000Genomes_30x NC_000006.12 - 31493374 Oct 17, 2022 (156)
62 The Avon Longitudinal Study of Parents and Children NC_000006.11 - 31461151 Oct 12, 2018 (152)
63 The Danish reference pan genome NC_000006.11 - 31461151 Apr 26, 2020 (154)
64 gnomAD - Genomes NC_000006.12 - 31493374 Apr 26, 2021 (155)
65 Genome of the Netherlands Release 5 NC_000006.11 - 31461151 Apr 26, 2020 (154)
66 HapMap NC_000006.12 - 31493374 Apr 26, 2020 (154)
67 KOREAN population from KRGDB NC_000006.11 - 31461151 Apr 26, 2020 (154)
68 Northern Sweden NC_000006.11 - 31461151 Jul 13, 2019 (153)
69 Qatari NC_000006.11 - 31461151 Apr 26, 2020 (154)
70 SGDP_PRJ NC_000006.11 - 31461151 Apr 26, 2020 (154)
71 Siberian NC_000006.11 - 31461151 Apr 26, 2020 (154)
72 8.3KJPN NC_000006.11 - 31461151 Apr 26, 2021 (155)
73 14KJPN NC_000006.12 - 31493374 Oct 17, 2022 (156)
74 TopMed NC_000006.12 - 31493374 Apr 26, 2021 (155)
75 UK 10K study - Twins NC_000006.11 - 31461151 Oct 12, 2018 (152)
76 A Vietnamese Genetic Variation Database NC_000006.11 - 31461151 Jul 13, 2019 (153)
77 ALFA NC_000006.12 - 31493374 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)
rs73390381 Dec 02, 2009 (131)
rs115468007 Oct 26, 2010 (133)
rs117718564 Aug 16, 2010 (132)
rs145655649 May 04, 2012 (137)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
18206193, ss3911028799 NC_000006.11:31461150:T:C NC_000006.12:31493373:T:C (self)
ss114143469, ss160597654, ss163347057, ss207414973, ss278726521, ss293825679, ss1592309332 NC_000006.10:31569129:T:G NC_000006.12:31493373:T:G (self)
31323915, 17465933, 7771260, 7764247, 18206193, 6646014, 8059780, 16271075, 4324616, 34804483, 17465933, 3873219, ss222303739, ss233398760, ss240469503, ss481605022, ss559113743, ss653034885, ss982765407, ss1073505388, ss1319556574, ss1581606321, ss1615276553, ss1658270586, ss1804357840, ss1926017850, ss1970357272, ss2023641903, ss2151808262, ss2626308256, ss2707402035, ss2998795089, ss3636778020, ss3733361149, ss3764821870, ss3829832416, ss3838394448, ss3864254095, ss3911028799, ss5176835176, ss5508427959, ss5640088753, ss5842026230, ss5968590565 NC_000006.11:31461150:T:G NC_000006.12:31493373:T:G (self)
41117022, 221206246, 3099918, 48526574, 535754769, 3016552513, ss3025608046, ss3648309830, ss3716907673, ss3807977261, ss3843836623, ss4698377211, ss5267935349, ss5465669623, ss5553591087, ss5714689470, ss5807306992, ss5855283599, ss5883242533 NC_000006.12:31493373:T:G NC_000006.12:31493373:T:G (self)
ss4099281, ss42659282, ss52085710, ss244292875 NT_007592.15:31401150:T:G NC_000006.12:31493373:T:G (self)
ss4025188429 NT_113891.3:2970714:T:G NC_000006.12:31493373:T:G (self)
ss4025247853 NT_167247.2:2835328:T:G NC_000006.12:31493373:T:G (self)
ss4025287428 NT_167249.2:2792650:T:G NC_000006.12:31493373:T:G (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 rs2904596

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