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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 Aliases 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.

rs2290400

Current Build 153

Released July 9, 2019

Organism
Homo sapiens
Position
chr17:39909987 (GRCh38.p12) 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
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.46203 (58016/125568, TOPMED)
C=0.4238 (33341/78680, PAGE_STUDY)
C=0.4810 (15057/31302, GnomAD) (+ 6 more)
C=0.421 (2106/5008, 1000G)
C=0.497 (2227/4480, Estonian)
T=0.491 (1894/3854, ALSPAC)
T=0.497 (1844/3708, TWINSUK)
T=0.48 (286/600, NorthernSweden)
C=0.24 (51/212, Vietnamese)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
GSDMB : Intron Variant
Publications
25 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.p12 chr 17 NC_000017.11:g.39909987T>C
GRCh37.p13 chr 17 NC_000017.10:g.38066240T>C
GSDMB RefSeqGene NG_015804.1:g.13664A>G
Gene: GSDMB, gasdermin B (minus strand)
Molecule type Change Amino acid[Codon] SO Term
GSDMB transcript variant 1 NM_001042471.1:c. N/A Intron Variant
GSDMB transcript variant 3 NM_001165958.1:c. N/A Intron Variant
GSDMB transcript variant 4 NM_001165959.1:c. N/A Intron Variant
GSDMB transcript variant 5 NM_001369402.1:c. N/A Intron Variant
GSDMB transcript variant 2 NM_018530.2:c. 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

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 125568 T=0.53797 C=0.46203
The PAGE Study Global Study-wide 78680 T=0.5762 C=0.4238
The PAGE Study AfricanAmerican Sub 32514 T=0.5220 C=0.4780
The PAGE Study Mexican Sub 10806 T=0.6247 C=0.3753
The PAGE Study Asian Sub 8316 T=0.734 C=0.266
The PAGE Study PuertoRican Sub 7916 T=0.545 C=0.455
The PAGE Study NativeHawaiian Sub 4532 T=0.623 C=0.377
The PAGE Study Cuban Sub 4224 T=0.555 C=0.445
The PAGE Study Dominican Sub 3828 T=0.556 C=0.444
The PAGE Study CentralAmerican Sub 2448 T=0.597 C=0.403
The PAGE Study SouthAmerican Sub 1982 T=0.600 C=0.400
The PAGE Study NativeAmerican Sub 1258 T=0.590 C=0.410
The PAGE Study SouthAsian Sub 856 T=0.59 C=0.41
gnomAD - Genomes Global Study-wide 31302 T=0.5190 C=0.4810
gnomAD - Genomes European Sub 18850 T=0.4985 C=0.5015
gnomAD - Genomes African Sub 8690 T=0.518 C=0.482
gnomAD - Genomes East Asian Sub 1548 T=0.738 C=0.262
gnomAD - Genomes Other Sub 1078 T=0.491 C=0.509
gnomAD - Genomes American Sub 846 T=0.62 C=0.38
gnomAD - Genomes Ashkenazi Jewish Sub 290 T=0.53 C=0.47
1000Genomes Global Study-wide 5008 T=0.579 C=0.421
1000Genomes African Sub 1322 T=0.511 C=0.489
1000Genomes East Asian Sub 1008 T=0.706 C=0.294
1000Genomes Europe Sub 1006 T=0.491 C=0.509
1000Genomes South Asian Sub 978 T=0.62 C=0.38
1000Genomes American Sub 694 T=0.60 C=0.40
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.503 C=0.497
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.491 C=0.509
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.497 C=0.503
Northern Sweden ACPOP Study-wide 600 T=0.48 C=0.52
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.76 C=0.24
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 Note
GRCh38.p12 chr 17 NC_000017.11:g.39909987= NC_000017.11:g.39909987T>C
GRCh37.p13 chr 17 NC_000017.10:g.38066240= NC_000017.10:g.38066240T>C
GSDMB RefSeqGene NG_015804.1:g.13664= NG_015804.1:g.13664A>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#.

126 SubSNP, 9 Frequency submissions
No Submitter Submission ID Date (Build)
1 YUSUKE ss3232262 Sep 28, 2001 (100)
2 SSAHASNP ss21402605 Apr 05, 2004 (121)
3 ABI ss44018534 Mar 15, 2006 (126)
4 AFFY ss66038059 Dec 01, 2006 (127)
5 ILLUMINA ss66775651 Dec 01, 2006 (127)
6 ILLUMINA ss67242966 Dec 01, 2006 (127)
7 ILLUMINA ss67639802 Dec 01, 2006 (127)
8 ILLUMINA ss70721310 May 25, 2008 (130)
9 ILLUMINA ss71289726 May 17, 2007 (127)
10 ILLUMINA ss75765944 Dec 07, 2007 (129)
11 AFFY ss75928661 Dec 08, 2007 (130)
12 ILLUMINA ss79127142 Dec 15, 2007 (130)
13 KRIBB_YJKIM ss84023898 Dec 15, 2007 (130)
14 BCMHGSC_JDW ss90584960 Mar 24, 2008 (129)
15 HUMANGENOME_JCVI ss96545188 Feb 05, 2009 (130)
16 1000GENOMES ss109756374 Jan 24, 2009 (130)
17 1000GENOMES ss113519961 Jan 25, 2009 (130)
18 ILLUMINA-UK ss118050892 Feb 14, 2009 (130)
19 ILLUMINA ss121988917 Dec 01, 2009 (131)
20 ENSEMBL ss136572582 Dec 01, 2009 (131)
21 ENSEMBL ss137064933 Dec 01, 2009 (131)
22 ILLUMINA ss153900192 Dec 01, 2009 (131)
23 ILLUMINA ss159378022 Dec 01, 2009 (131)
24 ILLUMINA ss160530355 Dec 01, 2009 (131)
25 COMPLETE_GENOMICS ss168122424 Jul 04, 2010 (132)
26 COMPLETE_GENOMICS ss169579104 Jul 04, 2010 (132)
27 ILLUMINA ss171166962 Jul 04, 2010 (132)
28 COMPLETE_GENOMICS ss171373734 Jul 04, 2010 (132)
29 ILLUMINA ss173258575 Jul 04, 2010 (132)
30 BUSHMAN ss202495695 Jul 04, 2010 (132)
31 1000GENOMES ss227541383 Jul 14, 2010 (132)
32 1000GENOMES ss237238620 Jul 15, 2010 (132)
33 1000GENOMES ss243538370 Jul 15, 2010 (132)
34 GMI ss282760377 May 04, 2012 (137)
35 GMI ss287178491 Apr 25, 2013 (138)
36 PJP ss292048022 May 09, 2011 (134)
37 ILLUMINA ss410821938 Sep 17, 2011 (135)
38 ILLUMINA ss480512542 May 04, 2012 (137)
39 ILLUMINA ss480526798 May 04, 2012 (137)
40 ILLUMINA ss481335813 Sep 08, 2015 (146)
41 ILLUMINA ss485053670 May 04, 2012 (137)
42 EXOME_CHIP ss491521399 May 04, 2012 (137)
43 ILLUMINA ss537071309 Sep 08, 2015 (146)
44 TISHKOFF ss565263205 Apr 25, 2013 (138)
45 SSMP ss661065112 Apr 25, 2013 (138)
46 ILLUMINA ss780673289 Sep 08, 2015 (146)
47 ILLUMINA ss780683284 Sep 08, 2015 (146)
48 ILLUMINA ss782973048 Sep 08, 2015 (146)
49 ILLUMINA ss783356673 Sep 08, 2015 (146)
50 ILLUMINA ss783934452 Sep 08, 2015 (146)
51 ILLUMINA ss825457660 Apr 01, 2015 (144)
52 ILLUMINA ss832229409 Sep 08, 2015 (146)
53 ILLUMINA ss832889818 Jul 13, 2019 (153)
54 ILLUMINA ss836169445 Sep 08, 2015 (146)
55 EVA-GONL ss993090955 Aug 21, 2014 (142)
56 JMKIDD_LAB ss1081047373 Aug 21, 2014 (142)
57 1000GENOMES ss1358583235 Aug 21, 2014 (142)
58 HAMMER_LAB ss1397730169 Sep 08, 2015 (146)
59 DDI ss1428028953 Apr 01, 2015 (144)
60 EVA_GENOME_DK ss1578151096 Apr 01, 2015 (144)
61 EVA_UK10K_ALSPAC ss1635617250 Apr 01, 2015 (144)
62 EVA_UK10K_TWINSUK ss1678611283 Apr 01, 2015 (144)
63 EVA_DECODE ss1697133049 Apr 01, 2015 (144)
64 EVA_MGP ss1711459068 Apr 01, 2015 (144)
65 EVA_SVP ss1713581420 Apr 01, 2015 (144)
66 ILLUMINA ss1752224251 Sep 08, 2015 (146)
67 ILLUMINA ss1752224252 Sep 08, 2015 (146)
68 HAMMER_LAB ss1808775129 Sep 08, 2015 (146)
69 ILLUMINA ss1917917831 Feb 12, 2016 (147)
70 WEILL_CORNELL_DGM ss1936550447 Feb 12, 2016 (147)
71 ILLUMINA ss1946444972 Feb 12, 2016 (147)
72 ILLUMINA ss1959744317 Feb 12, 2016 (147)
73 JJLAB ss2029053059 Sep 14, 2016 (149)
74 ILLUMINA ss2094894780 Dec 20, 2016 (150)
75 ILLUMINA ss2095074018 Dec 20, 2016 (150)
76 USC_VALOUEV ss2157521717 Dec 20, 2016 (150)
77 HUMAN_LONGEVITY ss2216701846 Dec 20, 2016 (150)
78 TOPMED ss2381803303 Dec 20, 2016 (150)
79 SYSTEMSBIOZJU ss2629022220 Nov 08, 2017 (151)
80 ILLUMINA ss2633394812 Nov 08, 2017 (151)
81 ILLUMINA ss2633394813 Nov 08, 2017 (151)
82 ILLUMINA ss2633394814 Nov 08, 2017 (151)
83 ILLUMINA ss2635070078 Nov 08, 2017 (151)
84 GRF ss2702083151 Nov 08, 2017 (151)
85 GNOMAD ss2949663230 Nov 08, 2017 (151)
86 AFFY ss2985094329 Nov 08, 2017 (151)
87 AFFY ss2985730857 Nov 08, 2017 (151)
88 SWEGEN ss3015504727 Nov 08, 2017 (151)
89 ILLUMINA ss3021777100 Nov 08, 2017 (151)
90 BIOINF_KMB_FNS_UNIBA ss3028346778 Nov 08, 2017 (151)
91 TOPMED ss3262338210 Nov 08, 2017 (151)
92 CSHL ss3351739020 Nov 08, 2017 (151)
93 ILLUMINA ss3627664855 Oct 12, 2018 (152)
94 ILLUMINA ss3627664856 Oct 12, 2018 (152)
95 ILLUMINA ss3631376097 Oct 12, 2018 (152)
96 ILLUMINA ss3633141011 Oct 12, 2018 (152)
97 ILLUMINA ss3633848482 Oct 12, 2018 (152)
98 ILLUMINA ss3634673914 Oct 12, 2018 (152)
99 ILLUMINA ss3634673915 Oct 12, 2018 (152)
100 ILLUMINA ss3635536258 Oct 12, 2018 (152)
101 ILLUMINA ss3636363980 Oct 12, 2018 (152)
102 ILLUMINA ss3637287799 Oct 12, 2018 (152)
103 ILLUMINA ss3638160030 Oct 12, 2018 (152)
104 ILLUMINA ss3639089725 Oct 12, 2018 (152)
105 ILLUMINA ss3639551807 Oct 12, 2018 (152)
106 ILLUMINA ss3640381227 Oct 12, 2018 (152)
107 ILLUMINA ss3640381228 Oct 12, 2018 (152)
108 ILLUMINA ss3643138630 Oct 12, 2018 (152)
109 ILLUMINA ss3644687272 Oct 12, 2018 (152)
110 OMUKHERJEE_ADBS ss3646510589 Oct 12, 2018 (152)
111 URBANLAB ss3650650770 Oct 12, 2018 (152)
112 ILLUMINA ss3652192577 Oct 12, 2018 (152)
113 ILLUMINA ss3652192578 Oct 12, 2018 (152)
114 ILLUMINA ss3653866085 Oct 12, 2018 (152)
115 EGCUT_WGS ss3682395600 Jul 13, 2019 (153)
116 EVA_DECODE ss3700430915 Jul 13, 2019 (153)
117 ILLUMINA ss3725619027 Jul 13, 2019 (153)
118 ACPOP ss3742011627 Jul 13, 2019 (153)
119 ILLUMINA ss3744443115 Jul 13, 2019 (153)
120 ILLUMINA ss3744974214 Jul 13, 2019 (153)
121 ILLUMINA ss3744974215 Jul 13, 2019 (153)
122 EVA ss3754646566 Jul 13, 2019 (153)
123 PAGE_CC ss3771925792 Jul 13, 2019 (153)
124 ILLUMINA ss3772472112 Jul 13, 2019 (153)
125 ILLUMINA ss3772472113 Jul 13, 2019 (153)
126 KHV_HUMAN_GENOMES ss3819917610 Jul 13, 2019 (153)
127 1000Genomes NC_000017.10 - 38066240 Oct 12, 2018 (152)
128 The Avon Longitudinal Study of Parents and Children NC_000017.10 - 38066240 Oct 12, 2018 (152)
129 Genetic variation in the Estonian population NC_000017.10 - 38066240 Oct 12, 2018 (152)
130 gnomAD - Genomes NC_000017.10 - 38066240 Jul 13, 2019 (153)
131 Northern Sweden NC_000017.10 - 38066240 Jul 13, 2019 (153)
132 The PAGE Study NC_000017.11 - 39909987 Jul 13, 2019 (153)
133 TopMed NC_000017.11 - 39909987 Oct 12, 2018 (152)
134 UK 10K study - Twins NC_000017.10 - 38066240 Oct 12, 2018 (152)
135 A Vietnamese Genetic Variation Database NC_000017.10 - 38066240 Jul 13, 2019 (153)
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)
rs56613831 May 27, 2008 (130)
rs59086175 May 25, 2008 (130)
rs386563857 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss90584960, ss109756374, ss113519961, ss118050892, ss168122424, ss169579104, ss171373734, ss202495695, ss282760377, ss287178491, ss292048022, ss480512542, ss825457660, ss1397730169, ss1697133049, ss1713581420, ss2094894780, ss2635070078, ss3639089725, ss3639551807, ss3643138630 NC_000017.9:35319765:T:C NC_000017.11:39909986:T:C (self)
71822373, 39809057, 28133848, 195982915, 15296492, 39809057, 8810802, ss227541383, ss237238620, ss243538370, ss480526798, ss481335813, ss485053670, ss491521399, ss537071309, ss565263205, ss661065112, ss780673289, ss780683284, ss782973048, ss783356673, ss783934452, ss832229409, ss832889818, ss836169445, ss993090955, ss1081047373, ss1358583235, ss1428028953, ss1578151096, ss1635617250, ss1678611283, ss1711459068, ss1752224251, ss1752224252, ss1808775129, ss1917917831, ss1936550447, ss1946444972, ss1959744317, ss2029053059, ss2095074018, ss2157521717, ss2381803303, ss2629022220, ss2633394812, ss2633394813, ss2633394814, ss2702083151, ss2949663230, ss2985094329, ss2985730857, ss3015504727, ss3021777100, ss3351739020, ss3627664855, ss3627664856, ss3631376097, ss3633141011, ss3633848482, ss3634673914, ss3634673915, ss3635536258, ss3636363980, ss3637287799, ss3638160030, ss3640381227, ss3640381228, ss3644687272, ss3646510589, ss3652192577, ss3652192578, ss3653866085, ss3682395600, ss3742011627, ss3744443115, ss3744974214, ss3744974215, ss3754646566, ss3772472112, ss3772472113 NC_000017.10:38066239:T:C NC_000017.11:39909986:T:C (self)
1147261, 156566083, ss2216701846, ss3028346778, ss3262338210, ss3650650770, ss3700430915, ss3725619027, ss3771925792, ss3819917610 NC_000017.11:39909986:T:C NC_000017.11:39909986:T:C (self)
ss21402605 NT_010755.14:1790535:T:C NC_000017.11:39909986:T:C (self)
ss3232262, ss44018534, ss66038059, ss66775651, ss67242966, ss67639802, ss70721310, ss71289726, ss75765944, ss75928661, ss79127142, ss84023898, ss96545188, ss121988917, ss136572582, ss137064933, ss153900192, ss159378022, ss160530355, ss171166962, ss173258575, ss410821938 NT_010783.15:3340391:T:C NC_000017.11:39909986:T:C (self)
Help

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

25 citations for rs2290400
PMID Title Author Year Journal
19426955 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Himes BE et al. 2009 American journal of human genetics
19430480 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Barrett JC et al. 2009 Nature genetics
19714205 Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. Hancock DB et al. 2009 PLoS genetics
19732864 Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. Verlaan DJ et al. 2009 American journal of human genetics
20372189 A sequence variant on 17q21 is associated with age at onset and severity of asthma. Halapi E et al. 2010 European journal of human genetics
20587799 Genetics of type 1 diabetes: what's next? Pociot F et al. 2010 Diabetes
20805105 Synthetic associations in the context of genome-wide association scan signals. Orozco G et al. 2010 Human molecular genetics
20833654 Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes. Murphy A et al. 2010 Human molecular genetics
20885991 Advances and challenges in biomarker development for type 1 diabetes prediction and prevention using omic technologies. Carey C et al. 2010 Expert opinion on medical diagnostics
21266329 Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs. Morahan G et al. 2011 Diabetes
21852963 Pervasive sharing of genetic effects in autoimmune disease. Cotsapas C et al. 2011 PLoS genetics
21873553 Genetic analysis of adult-onset autoimmune diabetes. Howson JM et al. 2011 Diabetes
21980299 A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. Bradfield JP et al. 2011 PLoS genetics
22069270 Genetic association analyses of atopic illness and proinflammatory cytokine genes with type 1 diabetes. Saleh NM et al. 2011 Diabetes/metabolism research and reviews
22190364 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Patsopoulos NA et al. 2011 Annals of neurology
22278338 Confirmation of novel type 1 diabetes risk loci in families. Cooper JD et al. 2012 Diabetologia
22626592 17q12-21 variants are associated with asthma and interact with active smoking in an adult population from the United Kingdom. Marinho S et al. 2012 Annals of allergy, asthma & immunology
23755072 Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. Li L et al. 2013 Frontiers in genetics
23923021 From interaction to co-association --a Fisher r-to-z transformation-based simple statistic for real world genome-wide association study. Yuan Z et al. 2013 PloS one
24968232 Regulation of gene expression in autoimmune disease loci and the genetic basis of proliferation in CD4+ effector memory T cells. Hu X et al. 2014 PLoS genetics
25904084 Genetic link of type 1 diabetes susceptibility loci with rheumatoid arthritis in Pakistani patients. Kiani AK et al. 2015 Immunogenetics
26575599 The Early Development of Wheeze. Environmental Determinants and Genetic Susceptibility at 17q21. Loss GJ et al. 2016 American journal of respiratory and critical care medicine
26904692 Genetic Risk Score Modelling for Disease Progression in New-Onset Type 1 Diabetes Patients: Increased Genetic Load of Islet-Expressed and Cytokine-Regulated Candidate Genes Predicts Poorer Glycemic Control. Brorsson CA et al. 2016 Journal of diabetes research
27352912 Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21. Ayabe T et al. 2016 Diabetic medicine
28347358 Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits. Grassmann F et al. 2017 Genome medicine

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.post308+0fe9b3b