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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.

rs61737145

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:44428408 (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
C>T
Variation Type
SNV Single Nucleotide Variation
Frequency
T=0.003918 (1037/264690, TOPMED)
T=0.003509 (882/251346, GnomAD_exome)
T=0.003843 (539/140240, GnomAD) (+ 14 more)
T=0.003827 (463/120986, ExAC)
T=0.00472 (233/49334, ALFA)
T=0.00500 (65/13006, GO-ESP)
T=0.0020 (13/6404, 1000G_30x)
T=0.0020 (10/5008, 1000G)
T=0.0007 (3/4480, Estonian)
T=0.0083 (32/3854, ALSPAC)
T=0.0038 (14/3708, TWINSUK)
T=0.004 (4/998, GoNL)
T=0.013 (8/600, NorthernSweden)
T=0.009 (5/534, MGP)
T=0.03 (1/40, GENOME_DK)
C=0.5 (1/2, Siberian)
T=0.5 (1/2, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
HNF4A : Synonymous Variant
Publications
1 citation
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 65694 C=0.99528 T=0.00472
European Sub 47384 C=0.99458 T=0.00542
African Sub 8412 C=0.9983 T=0.0017
African Others Sub 306 C=1.000 T=0.000
African American Sub 8106 C=0.9983 T=0.0017
Asian Sub 168 C=1.000 T=0.000
East Asian Sub 112 C=1.000 T=0.000
Other Asian Sub 56 C=1.00 T=0.00
Latin American 1 Sub 500 C=0.998 T=0.002
Latin American 2 Sub 628 C=0.997 T=0.003
South Asian Sub 98 C=1.00 T=0.00
Other Sub 8504 C=0.9958 T=0.0042


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 C=0.996082 T=0.003918
gnomAD - Exomes Global Study-wide 251346 C=0.996491 T=0.003509
gnomAD - Exomes European Sub 135300 C=0.995292 T=0.004708
gnomAD - Exomes Asian Sub 49008 C=0.99843 T=0.00157
gnomAD - Exomes American Sub 34590 C=0.99754 T=0.00246
gnomAD - Exomes African Sub 16244 C=0.99791 T=0.00209
gnomAD - Exomes Ashkenazi Jewish Sub 10076 C=0.99811 T=0.00189
gnomAD - Exomes Other Sub 6128 C=0.9951 T=0.0049
gnomAD - Genomes Global Study-wide 140240 C=0.996157 T=0.003843
gnomAD - Genomes European Sub 75946 C=0.99513 T=0.00487
gnomAD - Genomes African Sub 42036 C=0.99745 T=0.00255
gnomAD - Genomes American Sub 13652 C=0.99663 T=0.00337
gnomAD - Genomes Ashkenazi Jewish Sub 3320 C=0.9967 T=0.0033
gnomAD - Genomes East Asian Sub 3134 C=0.9997 T=0.0003
gnomAD - Genomes Other Sub 2152 C=0.9981 T=0.0019
ExAC Global Study-wide 120986 C=0.996173 T=0.003827
ExAC Europe Sub 73056 C=0.99514 T=0.00486
ExAC Asian Sub 25144 C=0.99837 T=0.00163
ExAC American Sub 11544 C=0.99697 T=0.00303
ExAC African Sub 10342 C=0.99758 T=0.00242
ExAC Other Sub 900 C=0.992 T=0.008
Allele Frequency Aggregator Total Global 49334 C=0.99528 T=0.00472
Allele Frequency Aggregator European Sub 37296 C=0.99466 T=0.00534
Allele Frequency Aggregator Other Sub 7070 C=0.9962 T=0.0038
Allele Frequency Aggregator African Sub 3574 C=0.9989 T=0.0011
Allele Frequency Aggregator Latin American 2 Sub 628 C=0.997 T=0.003
Allele Frequency Aggregator Latin American 1 Sub 500 C=0.998 T=0.002
Allele Frequency Aggregator Asian Sub 168 C=1.000 T=0.000
Allele Frequency Aggregator South Asian Sub 98 C=1.00 T=0.00
GO Exome Sequencing Project Global Study-wide 13006 C=0.99500 T=0.00500
GO Exome Sequencing Project European American Sub 8600 C=0.9936 T=0.0064
GO Exome Sequencing Project African American Sub 4406 C=0.9977 T=0.0023
1000Genomes_30x Global Study-wide 6404 C=0.9980 T=0.0020
1000Genomes_30x African Sub 1786 C=0.9978 T=0.0022
1000Genomes_30x Europe Sub 1266 C=0.9961 T=0.0039
1000Genomes_30x South Asian Sub 1202 C=0.9975 T=0.0025
1000Genomes_30x East Asian Sub 1170 C=1.0000 T=0.0000
1000Genomes_30x American Sub 980 C=0.999 T=0.001
1000Genomes Global Study-wide 5008 C=0.9980 T=0.0020
1000Genomes African Sub 1322 C=0.9977 T=0.0023
1000Genomes East Asian Sub 1008 C=1.0000 T=0.0000
1000Genomes Europe Sub 1006 C=0.9960 T=0.0040
1000Genomes South Asian Sub 978 C=0.998 T=0.002
1000Genomes American Sub 694 C=0.999 T=0.001
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.9993 T=0.0007
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.9917 T=0.0083
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.9962 T=0.0038
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.996 T=0.004
Northern Sweden ACPOP Study-wide 600 C=0.987 T=0.013
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 C=0.991 T=0.009
The Danish reference pan genome Danish Study-wide 40 C=0.97 T=0.03
Siberian Global Study-wide 2 C=0.5 T=0.5
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 20 NC_000020.11:g.44428408C>T
GRCh37.p13 chr 20 NC_000020.10:g.43057048C>T
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.77608C>T
Gene: HNF4A, hepatocyte nuclear factor 4 alpha (plus strand)
Molecule type Change Amino acid[Codon] SO Term
HNF4A transcript variant 6 NM_001030004.3:c. N/A Genic Downstream Transcript Variant
HNF4A transcript variant 10 NM_001287184.2:c. N/A Genic Downstream Transcript Variant
HNF4A transcript variant 3 NM_178850.3:c. N/A Genic Downstream Transcript Variant
HNF4A transcript variant 8 NM_001287182.2:c.1128C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 8 NP_001274111.1:p.Asn376= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 7 NM_001258355.2:c.1182C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 7 NP_001245284.1:p.Asn394= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 4 NM_001030003.3:c.1137C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 4 NP_001025174.1:p.Asn379= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 1 NM_178849.3:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 1 NP_849180.1:p.Asn401= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 5 NM_175914.5:c.1137C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 5 NP_787110.2:p.Asn379= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 9 NM_001287183.2:c.1128C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 9 NP_001274112.1:p.Asn376= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant 2 NM_000457.6:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform 2 NP_000448.3:p.Asn401= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant X1 XM_047440135.1:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296091.1:p.Asn401= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant X2 XM_047440136.1:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296092.1:p.Asn401= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant X3 XM_047440137.1:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296093.1:p.Asn401= N (Asn) > N (Asn) Synonymous Variant
HNF4A transcript variant X4 XM_047440138.1:c.1203C>T N [AAC] > N [AAT] Coding Sequence Variant
hepatocyte nuclear factor 4-alpha isoform X2 XP_047296094.1:p.Asn401= N (Asn) > N (Asn) Synonymous 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.

Allele: T (allele ID: 45007 )
ClinVar Accession Disease Names Clinical Significance
RCV000030013.5 Maturity-onset diabetes of the young type 1 Benign-Likely-Benign
RCV000243741.6 not specified Benign
RCV000954523.7 not provided Benign-Likely-Benign
RCV001139382.3 Familial hyperinsulinism Likely-Benign
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 C= T
GRCh38.p14 chr 20 NC_000020.11:g.44428408= NC_000020.11:g.44428408C>T
GRCh37.p13 chr 20 NC_000020.10:g.43057048= NC_000020.10:g.43057048C>T
HNF4A RefSeqGene (LRG_483) NG_009818.1:g.77608= NG_009818.1:g.77608C>T
HNF4A transcript variant 2 NM_000457.4:c.1203= NM_000457.4:c.1203C>T
HNF4A transcript variant 2 NM_000457.6:c.1203= NM_000457.6:c.1203C>T
HNF4A transcript variant 2 NM_000457.5:c.1203= NM_000457.5:c.1203C>T
HNF4A transcript variant 5 NM_175914.4:c.1137= NM_175914.4:c.1137C>T
HNF4A transcript variant 5 NM_175914.5:c.1137= NM_175914.5:c.1137C>T
HNF4A transcript variant 1 NM_178849.3:c.1203= NM_178849.3:c.1203C>T
HNF4A transcript variant 1 NM_178849.2:c.1203= NM_178849.2:c.1203C>T
HNF4A transcript variant 4 NM_001030003.3:c.1137= NM_001030003.3:c.1137C>T
HNF4A transcript variant 4 NM_001030003.2:c.1137= NM_001030003.2:c.1137C>T
HNF4A transcript variant 8 NM_001287182.2:c.1128= NM_001287182.2:c.1128C>T
HNF4A transcript variant 8 NM_001287182.1:c.1128= NM_001287182.1:c.1128C>T
HNF4A transcript variant 7 NM_001258355.2:c.1182= NM_001258355.2:c.1182C>T
HNF4A transcript variant 7 NM_001258355.1:c.1182= NM_001258355.1:c.1182C>T
HNF4A transcript variant 9 NM_001287183.1:c.1128= NM_001287183.1:c.1128C>T
HNF4A transcript variant 9 NM_001287183.2:c.1128= NM_001287183.2:c.1128C>T
HNF4A transcript variant X4 XM_047440138.1:c.1203= XM_047440138.1:c.1203C>T
HNF4A transcript variant X1 XM_047440135.1:c.1203= XM_047440135.1:c.1203C>T
HNF4A transcript variant X2 XM_047440136.1:c.1203= XM_047440136.1:c.1203C>T
HNF4A transcript variant X3 XM_047440137.1:c.1203= XM_047440137.1:c.1203C>T
hepatocyte nuclear factor 4-alpha isoform 2 NP_000448.3:p.Asn401= NP_000448.3:p.Asn401=
hepatocyte nuclear factor 4-alpha isoform 5 NP_787110.2:p.Asn379= NP_787110.2:p.Asn379=
hepatocyte nuclear factor 4-alpha isoform 1 NP_849180.1:p.Asn401= NP_849180.1:p.Asn401=
hepatocyte nuclear factor 4-alpha isoform 4 NP_001025174.1:p.Asn379= NP_001025174.1:p.Asn379=
hepatocyte nuclear factor 4-alpha isoform 8 NP_001274111.1:p.Asn376= NP_001274111.1:p.Asn376=
hepatocyte nuclear factor 4-alpha isoform 7 NP_001245284.1:p.Asn394= NP_001245284.1:p.Asn394=
hepatocyte nuclear factor 4-alpha isoform 9 NP_001274112.1:p.Asn376= NP_001274112.1:p.Asn376=
hepatocyte nuclear factor 4-alpha isoform X2 XP_047296094.1:p.Asn401= XP_047296094.1:p.Asn401=
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296091.1:p.Asn401= XP_047296091.1:p.Asn401=
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296092.1:p.Asn401= XP_047296092.1:p.Asn401=
hepatocyte nuclear factor 4-alpha isoform X1 XP_047296093.1:p.Asn401= XP_047296093.1:p.Asn401=
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#.

44 SubSNP, 16 Frequency, 4 ClinVar submissions
No Submitter Submission ID Date (Build)
1 CORNELL ss86245782 Mar 23, 2008 (129)
2 1000GENOMES ss112012121 Jan 25, 2009 (130)
3 SEATTLESEQ ss159742397 Dec 01, 2009 (131)
4 1000GENOMES ss340772005 May 09, 2011 (134)
5 NHLBI-ESP ss342522536 May 09, 2011 (134)
6 ILLUMINA ss410839628 Sep 17, 2011 (135)
7 CORRELAGEN ss472343391 Nov 18, 2011 (136)
8 1000GENOMES ss491177543 May 04, 2012 (137)
9 CLINSEQ_SNP ss491810049 May 04, 2012 (137)
10 EVA-GONL ss994753975 Aug 21, 2014 (142)
11 1000GENOMES ss1364906282 Aug 21, 2014 (142)
12 EVA_GENOME_DK ss1579517893 Apr 01, 2015 (144)
13 EVA_UK10K_ALSPAC ss1638852036 Apr 01, 2015 (144)
14 EVA_UK10K_TWINSUK ss1681846069 Apr 01, 2015 (144)
15 EVA_EXAC ss1694005618 Apr 01, 2015 (144)
16 EVA_DECODE ss1698814205 Apr 01, 2015 (144)
17 EVA_MGP ss1711541736 Apr 01, 2015 (144)
18 JJLAB ss2029913980 Sep 14, 2016 (149)
19 USC_VALOUEV ss2158481314 Dec 20, 2016 (150)
20 HUMAN_LONGEVITY ss2243038333 Dec 20, 2016 (150)
21 GNOMAD ss2744621478 Nov 08, 2017 (151)
22 GNOMAD ss2750387082 Nov 08, 2017 (151)
23 GNOMAD ss2967808397 Nov 08, 2017 (151)
24 SWEGEN ss3018235707 Nov 08, 2017 (151)
25 EGCUT_WGS ss3684921939 Jul 13, 2019 (153)
26 EVA_DECODE ss3707011653 Jul 13, 2019 (153)
27 ACPOP ss3743420732 Jul 13, 2019 (153)
28 EVA ss3825373396 Apr 27, 2020 (154)
29 EVA ss3825953345 Apr 27, 2020 (154)
30 EVA ss3835688104 Apr 27, 2020 (154)
31 EVA ss3841468286 Apr 27, 2020 (154)
32 EVA ss3846981159 Apr 27, 2020 (154)
33 EVA ss3986832087 Apr 27, 2021 (155)
34 TOPMED ss5089806694 Apr 27, 2021 (155)
35 EVA ss5237674506 Oct 16, 2022 (156)
36 1000G_HIGH_COVERAGE ss5308916502 Oct 16, 2022 (156)
37 EVA ss5437626216 Oct 16, 2022 (156)
38 HUGCELL_USP ss5501183399 Oct 16, 2022 (156)
39 1000G_HIGH_COVERAGE ss5615436190 Oct 16, 2022 (156)
40 SANFORD_IMAGENETICS ss5663277837 Oct 16, 2022 (156)
41 EVA ss5845738677 Oct 16, 2022 (156)
42 EVA ss5848549042 Oct 16, 2022 (156)
43 EVA ss5923564572 Oct 16, 2022 (156)
44 EVA ss5958199101 Oct 16, 2022 (156)
45 1000Genomes NC_000020.10 - 43057048 Oct 12, 2018 (152)
46 1000Genomes_30x NC_000020.11 - 44428408 Oct 16, 2022 (156)
47 The Avon Longitudinal Study of Parents and Children NC_000020.10 - 43057048 Oct 12, 2018 (152)
48 Genetic variation in the Estonian population NC_000020.10 - 43057048 Oct 12, 2018 (152)
49 ExAC NC_000020.10 - 43057048 Oct 12, 2018 (152)
50 The Danish reference pan genome NC_000020.10 - 43057048 Apr 27, 2020 (154)
51 gnomAD - Genomes NC_000020.11 - 44428408 Apr 27, 2021 (155)
52 gnomAD - Exomes NC_000020.10 - 43057048 Jul 13, 2019 (153)
53 GO Exome Sequencing Project NC_000020.10 - 43057048 Oct 12, 2018 (152)
54 Genome of the Netherlands Release 5 NC_000020.10 - 43057048 Apr 27, 2020 (154)
55 Medical Genome Project healthy controls from Spanish population NC_000020.10 - 43057048 Apr 27, 2020 (154)
56 Northern Sweden NC_000020.10 - 43057048 Jul 13, 2019 (153)
57 Siberian NC_000020.10 - 43057048 Apr 27, 2020 (154)
58 TopMed NC_000020.11 - 44428408 Apr 27, 2021 (155)
59 UK 10K study - Twins NC_000020.10 - 43057048 Oct 12, 2018 (152)
60 ALFA NC_000020.11 - 44428408 Apr 27, 2021 (155)
61 ClinVar RCV000030013.5 Oct 16, 2022 (156)
62 ClinVar RCV000243741.6 Oct 16, 2022 (156)
63 ClinVar RCV000954523.7 Oct 16, 2022 (156)
64 ClinVar RCV001139382.3 Oct 16, 2022 (156)
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
ss112012121, ss491810049, ss1698814205 NC_000020.9:42490461:C:T NC_000020.11:44428407:C:T (self)
78374089, 43386309, 30660187, 5561077, 5682832, 13943343, 1830300, 19326054, 657496, 16705597, 10997668, 43386309, ss340772005, ss342522536, ss491177543, ss994753975, ss1364906282, ss1579517893, ss1638852036, ss1681846069, ss1694005618, ss1711541736, ss2029913980, ss2158481314, ss2744621478, ss2750387082, ss2967808397, ss3018235707, ss3684921939, ss3743420732, ss3825373396, ss3825953345, ss3835688104, ss3841468286, ss3986832087, ss5437626216, ss5663277837, ss5845738677, ss5848549042, ss5958199101 NC_000020.10:43057047:C:T NC_000020.11:44428407:C:T (self)
RCV000030013.5, RCV000243741.6, RCV000954523.7, RCV001139382.3, 102962125, 552842330, 364915639, 5398725056, ss472343391, ss2243038333, ss3707011653, ss3846981159, ss5089806694, ss5237674506, ss5308916502, ss5501183399, ss5615436190, ss5923564572 NC_000020.11:44428407:C:T NC_000020.11:44428407:C:T (self)
ss86245782, ss159742397, ss410839628 NT_011362.10:13253139:C:T NC_000020.11:44428407:C:T (self)
Help

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

1 citation for rs61737145
PMID Title Author Year Journal
25741868 Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Richards S et al. 2015 Genetics in medicine
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