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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 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.

rs4648344

Current Build 155

Released April 9, 2021

Organism
Homo sapiens
Position
chr1:3826568 (GRCh38.p13) 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
T=0.472749 (125132/264690, TOPMED)
T=0.455206 (63667/139864, GnomAD)
T=0.49597 (35406/71388, ALFA) (+ 18 more)
C=0.04732 (793/16760, 8.3KJPN)
C=0.4221 (2114/5008, 1000G)
C=0.4752 (2129/4480, Estonian)
C=0.4925 (1898/3854, ALSPAC)
C=0.4962 (1840/3708, TWINSUK)
C=0.0404 (118/2922, KOREAN)
C=0.3829 (798/2084, HGDP_Stanford)
C=0.4666 (881/1888, HapMap)
C=0.0480 (88/1832, Korea1K)
T=0.487 (486/998, GoNL)
C=0.475 (285/600, NorthernSweden)
C=0.062 (33/534, MGP)
T=0.290 (84/290, SGDP_PRJ)
T=0.417 (90/216, Qatari)
C=0.080 (17/212, Vietnamese)
C=0.47 (19/40, GENOME_DK)
C=0.30 (12/40, Ancient Sardinia)
T=0.33 (10/30, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
CEP104 : Intron Variant
Publications
1 citation
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.p13 chr 1 NC_000001.11:g.3826568T>C
GRCh37.p13 chr 1 NC_000001.10:g.3743132T>C
CEP104 RefSeqGene NG_046726.1:g.35666A>G
Gene: CEP104, centrosomal protein 104 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
CEP104 transcript NM_014704.4:c.2189-132A>G N/A Intron Variant
CEP104 transcript variant X2 XM_005244815.4:c.2297-132…

XM_005244815.4:c.2297-132A>G

N/A Intron Variant
CEP104 transcript variant X3 XM_011542474.3:c.2207-132…

XM_011542474.3:c.2207-132A>G

N/A Intron Variant
CEP104 transcript variant X7 XM_017002918.2:c.2015-132…

XM_017002918.2:c.2015-132A>G

N/A Intron Variant
CEP104 transcript variant X8 XM_017002919.2:c.1991-132…

XM_017002919.2:c.1991-132A>G

N/A Intron Variant
CEP104 transcript variant X1 XM_024451101.1:c.2315-132…

XM_024451101.1:c.2315-132A>G

N/A Intron Variant
CEP104 transcript variant X4 XM_024451102.1:c.2141-132…

XM_024451102.1:c.2141-132A>G

N/A Intron Variant
CEP104 transcript variant X5 XM_024451103.1:c.2123-132…

XM_024451103.1:c.2123-132A>G

N/A Intron Variant
CEP104 transcript variant X6 XM_024451104.1:c.2117-132…

XM_024451104.1:c.2117-132A>G

N/A Intron Variant
CEP104 transcript variant X9 XM_024451106.1:c.1943-132…

XM_024451106.1:c.1943-132A>G

N/A Intron Variant
CEP104 transcript variant X10 XM_024451108.1:c. N/A Genic Downstream Transcript 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

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: 20201027095038
Population Group Sample Size Ref Allele Alt Allele
Total Global 71388 T=0.49597 C=0.50403
European Sub 58762 T=0.49940 C=0.50060
African Sub 4526 T=0.2760 C=0.7240
African Others Sub 170 T=0.212 C=0.788
African American Sub 4356 T=0.2785 C=0.7215
Asian Sub 190 T=0.921 C=0.079
East Asian Sub 148 T=0.919 C=0.081
Other Asian Sub 42 T=0.93 C=0.07
Latin American 1 Sub 254 T=0.465 C=0.535
Latin American 2 Sub 1232 T=0.6794 C=0.3206
South Asian Sub 4954 T=0.5941 C=0.4059
Other Sub 1470 T=0.5020 C=0.4980


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=0.472749 C=0.527251
gnomAD - Genomes Global Study-wide 139864 T=0.455206 C=0.544794
gnomAD - Genomes European Sub 75718 T=0.49881 C=0.50119
gnomAD - Genomes African Sub 41906 T=0.28695 C=0.71305
gnomAD - Genomes American Sub 13638 T=0.62685 C=0.37315
gnomAD - Genomes Ashkenazi Jewish Sub 3320 T=0.3895 C=0.6105
gnomAD - Genomes East Asian Sub 3130 T=0.9514 C=0.0486
gnomAD - Genomes Other Sub 2152 T=0.4893 C=0.5107
8.3KJPN JAPANESE Study-wide 16760 T=0.95268 C=0.04732
1000Genomes Global Study-wide 5008 T=0.5779 C=0.4221
1000Genomes African Sub 1322 T=0.2564 C=0.7436
1000Genomes East Asian Sub 1008 T=0.9474 C=0.0526
1000Genomes Europe Sub 1006 T=0.5149 C=0.4851
1000Genomes South Asian Sub 978 T=0.633 C=0.367
1000Genomes American Sub 694 T=0.667 C=0.333
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.5248 C=0.4752
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.5075 C=0.4925
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.5038 C=0.4962
KOREAN population from KRGDB KOREAN Study-wide 2922 T=0.9596 C=0.0404
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 T=0.6171 C=0.3829
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 T=0.917 C=0.083
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 T=0.502 C=0.498
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 T=0.474 C=0.526
HGDP-CEPH-db Supplement 1 Europe Sub 320 T=0.491 C=0.509
HGDP-CEPH-db Supplement 1 Africa Sub 242 T=0.198 C=0.802
HGDP-CEPH-db Supplement 1 America Sub 216 T=0.972 C=0.028
HGDP-CEPH-db Supplement 1 Oceania Sub 72 T=0.92 C=0.08
HapMap Global Study-wide 1888 T=0.5334 C=0.4666
HapMap American Sub 770 T=0.660 C=0.340
HapMap African Sub 688 T=0.235 C=0.765
HapMap Asian Sub 254 T=0.976 C=0.024
HapMap Europe Sub 176 T=0.506 C=0.494
Korean Genome Project KOREAN Study-wide 1832 T=0.9520 C=0.0480
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.487 C=0.513
Northern Sweden ACPOP Study-wide 600 T=0.525 C=0.475
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.938 C=0.062
SGDP_PRJ Global Study-wide 290 T=0.290 C=0.710
Qatari Global Study-wide 216 T=0.417 C=0.583
A Vietnamese Genetic Variation Database Global Study-wide 212 T=0.920 C=0.080
The Danish reference pan genome Danish Study-wide 40 T=0.53 C=0.47
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 40 T=0.70 C=0.30
Siberian Global Study-wide 30 T=0.33 C=0.67
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
GRCh38.p13 chr 1 NC_000001.11:g.3826568= NC_000001.11:g.3826568T>C
GRCh37.p13 chr 1 NC_000001.10:g.3743132= NC_000001.10:g.3743132T>C
CEP104 RefSeqGene NG_046726.1:g.35666= NG_046726.1:g.35666A>G
CEP104 transcript NM_014704.3:c.2189-132= NM_014704.3:c.2189-132A>G
CEP104 transcript NM_014704.4:c.2189-132= NM_014704.4:c.2189-132A>G
CEP104 transcript variant X1 XM_005244815.1:c.2297-132= XM_005244815.1:c.2297-132A>G
CEP104 transcript variant X2 XM_005244815.4:c.2297-132= XM_005244815.4:c.2297-132A>G
CEP104 transcript variant X3 XM_011542474.3:c.2207-132= XM_011542474.3:c.2207-132A>G
CEP104 transcript variant X7 XM_017002918.2:c.2015-132= XM_017002918.2:c.2015-132A>G
CEP104 transcript variant X8 XM_017002919.2:c.1991-132= XM_017002919.2:c.1991-132A>G
CEP104 transcript variant X1 XM_024451101.1:c.2315-132= XM_024451101.1:c.2315-132A>G
CEP104 transcript variant X4 XM_024451102.1:c.2141-132= XM_024451102.1:c.2141-132A>G
CEP104 transcript variant X5 XM_024451103.1:c.2123-132= XM_024451103.1:c.2123-132A>G
CEP104 transcript variant X6 XM_024451104.1:c.2117-132= XM_024451104.1:c.2117-132A>G
CEP104 transcript variant X9 XM_024451106.1:c.1943-132= XM_024451106.1:c.1943-132A>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#.

95 SubSNP, 21 Frequency submissions
No Submitter Submission ID Date (Build)
1 WI_SSAHASNP ss6396331 Feb 20, 2003 (111)
2 CSHL-HAPMAP ss16435683 Feb 27, 2004 (120)
3 SSAHASNP ss20543050 Apr 05, 2004 (121)
4 PERLEGEN ss24243614 Sep 20, 2004 (123)
5 ABI ss44005681 Mar 13, 2006 (126)
6 ILLUMINA ss66842578 Nov 30, 2006 (127)
7 ILLUMINA ss67352853 Nov 30, 2006 (127)
8 ILLUMINA ss67743289 Nov 30, 2006 (127)
9 ILLUMINA ss70812955 May 25, 2008 (130)
10 ILLUMINA ss71393461 May 17, 2007 (127)
11 ILLUMINA ss75879262 Dec 06, 2007 (129)
12 ILLUMINA ss79187699 Dec 15, 2007 (130)
13 KRIBB_YJKIM ss84304096 Dec 15, 2007 (130)
14 HGSV ss85312462 Dec 15, 2007 (130)
15 BCMHGSC_JDW ss87174504 Mar 23, 2008 (129)
16 HUMANGENOME_JCVI ss97915510 Feb 05, 2009 (130)
17 1000GENOMES ss107949111 Jan 22, 2009 (130)
18 1000GENOMES ss109967742 Jan 24, 2009 (130)
19 ILLUMINA ss122343277 Dec 01, 2009 (131)
20 ENSEMBL ss137763630 Dec 01, 2009 (131)
21 ENSEMBL ss138971359 Dec 01, 2009 (131)
22 ILLUMINA ss154304361 Dec 01, 2009 (131)
23 ILLUMINA ss159481185 Dec 01, 2009 (131)
24 COMPLETE_GENOMICS ss163005066 Jul 04, 2010 (132)
25 COMPLETE_GENOMICS ss163738438 Jul 04, 2010 (132)
26 ILLUMINA ss171844690 Jul 04, 2010 (132)
27 ILLUMINA ss173767960 Jul 04, 2010 (132)
28 BUSHMAN ss197925245 Jul 04, 2010 (132)
29 BCM-HGSC-SUB ss205411032 Jul 04, 2010 (132)
30 1000GENOMES ss218203336 Jul 14, 2010 (132)
31 1000GENOMES ss230404214 Jul 14, 2010 (132)
32 1000GENOMES ss238123092 Jul 15, 2010 (132)
33 BL ss252880554 May 09, 2011 (134)
34 PJP ss290498350 May 09, 2011 (134)
35 GMI ss475580087 May 04, 2012 (137)
36 ILLUMINA ss537252853 Sep 08, 2015 (146)
37 TISHKOFF ss553734767 Apr 25, 2013 (138)
38 SSMP ss647536578 Apr 25, 2013 (138)
39 ILLUMINA ss825518217 Jul 19, 2016 (147)
40 ILLUMINA ss832992616 Aug 21, 2014 (142)
41 ILLUMINA ss833583445 Aug 21, 2014 (142)
42 EVA-GONL ss974796610 Aug 21, 2014 (142)
43 JMKIDD_LAB ss1067627400 Aug 21, 2014 (142)
44 1000GENOMES ss1289452174 Aug 21, 2014 (142)
45 DDI ss1425693067 Apr 01, 2015 (144)
46 EVA_GENOME_DK ss1573860199 Apr 01, 2015 (144)
47 EVA_DECODE ss1584155371 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1599427640 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1642421673 Apr 01, 2015 (144)
50 EVA_MGP ss1710885679 Apr 01, 2015 (144)
51 EVA_SVP ss1712306782 Apr 01, 2015 (144)
52 HAMMER_LAB ss1793785211 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1917992137 Feb 12, 2016 (147)
54 GENOMED ss1966671416 Jul 19, 2016 (147)
55 JJLAB ss2019512233 Sep 14, 2016 (149)
56 USC_VALOUEV ss2147502600 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2159575613 Dec 20, 2016 (150)
58 TOPMED ss2321730507 Dec 20, 2016 (150)
59 GRF ss2697396651 Nov 08, 2017 (151)
60 GNOMAD ss2750973588 Nov 08, 2017 (151)
61 SWEGEN ss2986201536 Nov 08, 2017 (151)
62 BIOINF_KMB_FNS_UNIBA ss3023519736 Nov 08, 2017 (151)
63 TOPMED ss3067129315 Nov 08, 2017 (151)
64 CSHL ss3343289030 Nov 08, 2017 (151)
65 ILLUMINA ss3626011955 Oct 11, 2018 (152)
66 ILLUMINA ss3637733771 Oct 11, 2018 (152)
67 ILLUMINA ss3638888279 Oct 11, 2018 (152)
68 ILLUMINA ss3639440887 Oct 11, 2018 (152)
69 ILLUMINA ss3642747983 Oct 11, 2018 (152)
70 OMUKHERJEE_ADBS ss3646220215 Oct 11, 2018 (152)
71 URBANLAB ss3646586797 Oct 11, 2018 (152)
72 EGCUT_WGS ss3654302743 Jul 12, 2019 (153)
73 EVA_DECODE ss3686047453 Jul 12, 2019 (153)
74 ACPOP ss3726740174 Jul 12, 2019 (153)
75 EVA ss3745755524 Jul 12, 2019 (153)
76 PACBIO ss3783308828 Jul 12, 2019 (153)
77 PACBIO ss3788985716 Jul 12, 2019 (153)
78 PACBIO ss3793858343 Jul 12, 2019 (153)
79 KHV_HUMAN_GENOMES ss3798777176 Jul 12, 2019 (153)
80 EVA ss3825551298 Apr 25, 2020 (154)
81 EVA ss3825994041 Apr 25, 2020 (154)
82 EVA ss3836384204 Apr 25, 2020 (154)
83 EVA ss3841788372 Apr 25, 2020 (154)
84 HGDP ss3847322572 Apr 25, 2020 (154)
85 SGDP_PRJ ss3848069780 Apr 25, 2020 (154)
86 KRGDB ss3892931436 Apr 25, 2020 (154)
87 KOGIC ss3943693139 Apr 25, 2020 (154)
88 FSA-LAB ss3983913142 Apr 25, 2021 (155)
89 FSA-LAB ss3983913143 Apr 25, 2021 (155)
90 EVA ss3984774952 Apr 25, 2021 (155)
91 EVA ss3986095383 Apr 25, 2021 (155)
92 EVA ss4016890116 Apr 25, 2021 (155)
93 TOPMED ss4437309124 Apr 25, 2021 (155)
94 TOMMO_GENOMICS ss5142202227 Apr 25, 2021 (155)
95 EVA ss5237158802 Apr 25, 2021 (155)
96 1000Genomes NC_000001.10 - 3743132 Oct 11, 2018 (152)
97 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 3743132 Oct 11, 2018 (152)
98 Genetic variation in the Estonian population NC_000001.10 - 3743132 Oct 11, 2018 (152)
99 The Danish reference pan genome NC_000001.10 - 3743132 Apr 25, 2020 (154)
100 gnomAD - Genomes NC_000001.11 - 3826568 Apr 25, 2021 (155)
101 Genome of the Netherlands Release 5 NC_000001.10 - 3743132 Apr 25, 2020 (154)
102 HGDP-CEPH-db Supplement 1 NC_000001.9 - 3732992 Apr 25, 2020 (154)
103 HapMap NC_000001.11 - 3826568 Apr 25, 2020 (154)
104 KOREAN population from KRGDB NC_000001.10 - 3743132 Apr 25, 2020 (154)
105 Korean Genome Project NC_000001.11 - 3826568 Apr 25, 2020 (154)
106 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 3743132 Apr 25, 2020 (154)
107 Northern Sweden NC_000001.10 - 3743132 Jul 12, 2019 (153)
108 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 3743132 Apr 25, 2021 (155)
109 Qatari NC_000001.10 - 3743132 Apr 25, 2020 (154)
110 SGDP_PRJ NC_000001.10 - 3743132 Apr 25, 2020 (154)
111 Siberian NC_000001.10 - 3743132 Apr 25, 2020 (154)
112 8.3KJPN NC_000001.10 - 3743132 Apr 25, 2021 (155)
113 TopMed NC_000001.11 - 3826568 Apr 25, 2021 (155)
114 UK 10K study - Twins NC_000001.10 - 3743132 Oct 11, 2018 (152)
115 A Vietnamese Genetic Variation Database NC_000001.10 - 3743132 Jul 12, 2019 (153)
116 ALFA NC_000001.11 - 3826568 Apr 25, 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)
rs17411962 Oct 07, 2004 (123)
rs59453361 May 25, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss85312462, ss3638888279, ss3639440887 NC_000001.8:3766288:T:C NC_000001.11:3826567:T:C (self)
464, ss87174504, ss107949111, ss109967742, ss163005066, ss163738438, ss197925245, ss205411032, ss252880554, ss290498350, ss475580087, ss825518217, ss1584155371, ss1712306782, ss3642747983, ss3847322572 NC_000001.9:3732991:T:C NC_000001.11:3826567:T:C (self)
120210, 53897, 40991, 1367433, 23213, 108830, 2431, 25039, 879, 34067, 86760, 18954, 171534, 53897, 11407, ss218203336, ss230404214, ss238123092, ss537252853, ss553734767, ss647536578, ss832992616, ss833583445, ss974796610, ss1067627400, ss1289452174, ss1425693067, ss1573860199, ss1599427640, ss1642421673, ss1710885679, ss1793785211, ss1917992137, ss1966671416, ss2019512233, ss2147502600, ss2321730507, ss2697396651, ss2750973588, ss2986201536, ss3343289030, ss3626011955, ss3637733771, ss3646220215, ss3654302743, ss3726740174, ss3745755524, ss3783308828, ss3788985716, ss3793858343, ss3825551298, ss3825994041, ss3836384204, ss3848069780, ss3892931436, ss3983913142, ss3983913143, ss3984774952, ss3986095383, ss4016890116, ss5142202227 NC_000001.10:3743131:T:C NC_000001.11:3826567:T:C (self)
866584, 2835, 71140, 569980, 915459, 4014213257, ss2159575613, ss3023519736, ss3067129315, ss3646586797, ss3686047453, ss3798777176, ss3841788372, ss3943693139, ss4437309124, ss5237158802 NC_000001.11:3826567:T:C NC_000001.11:3826567:T:C (self)
ss16435683, ss20543050 NT_004321.15:1049905:T:C NC_000001.11:3826567:T:C (self)
ss6396331, ss24243614, ss44005681, ss66842578, ss67352853, ss67743289, ss70812955, ss71393461, ss75879262, ss79187699, ss84304096, ss97915510, ss122343277, ss137763630, ss138971359, ss154304361, ss159481185, ss171844690, ss173767960 NT_004350.19:3221763:T:C NC_000001.11:3826567: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.

1 citation for rs4648344
PMID Title Author Year Journal
27316555 Proposed nomenclature for microhaplotypes. Kidd KK et al. 2016 Human genomics
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.post596+ae089ad