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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.

rs6603832

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:5067483 (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>G
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.319275 (84509/264690, TOPMED)
A=0.351822 (89369/254018, ALFA)
A=0.308441 (43204/140072, GnomAD) (+ 22 more)
A=0.35133 (27569/78470, PAGE_STUDY)
G=0.29114 (8227/28258, 14KJPN)
G=0.29031 (4865/16758, 8.3KJPN)
A=0.3857 (2470/6404, 1000G_30x)
A=0.3972 (1989/5008, 1000G)
A=0.3705 (1660/4480, Estonian)
A=0.3505 (1351/3854, ALSPAC)
A=0.3382 (1254/3708, TWINSUK)
G=0.2669 (782/2930, KOREAN)
A=0.3508 (663/1890, HapMap)
G=0.2931 (537/1832, Korea1K)
A=0.3677 (417/1134, Daghestan)
A=0.323 (322/998, GoNL)
G=0.292 (225/770, PRJEB37584)
A=0.405 (243/600, NorthernSweden)
A=0.318 (135/424, SGDP_PRJ)
A=0.352 (76/216, Qatari)
G=0.341 (73/214, Vietnamese)
G=0.37 (22/60, Ancient Sardinia)
A=0.33 (15/46, Siberian)
A=0.50 (20/40, GENOME_DK)
G=0.50 (20/40, GENOME_DK)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
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 259054 A=0.351008 G=0.648992
European Sub 223624 A=0.347700 G=0.652300
African Sub 11270 A=0.18997 G=0.81003
African Others Sub 412 A=0.141 G=0.859
African American Sub 10858 A=0.19184 G=0.80816
Asian Sub 3900 A=0.7223 G=0.2777
East Asian Sub 3138 A=0.7323 G=0.2677
Other Asian Sub 762 A=0.681 G=0.319
Latin American 1 Sub 1172 A=0.2961 G=0.7039
Latin American 2 Sub 8752 A=0.4584 G=0.5416
South Asian Sub 380 A=0.387 G=0.613
Other Sub 9956 A=0.3728 G=0.6272


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=0.319275 G=0.680725
Allele Frequency Aggregator Total Global 254018 A=0.351822 G=0.648178
Allele Frequency Aggregator European Sub 220530 A=0.347662 G=0.652338
Allele Frequency Aggregator African Sub 10128 A=0.19135 G=0.80865
Allele Frequency Aggregator Other Sub 9156 A=0.3755 G=0.6245
Allele Frequency Aggregator Latin American 2 Sub 8752 A=0.4584 G=0.5416
Allele Frequency Aggregator Asian Sub 3900 A=0.7223 G=0.2777
Allele Frequency Aggregator Latin American 1 Sub 1172 A=0.2961 G=0.7039
Allele Frequency Aggregator South Asian Sub 380 A=0.387 G=0.613
gnomAD - Genomes Global Study-wide 140072 A=0.308441 G=0.691559
gnomAD - Genomes European Sub 75848 A=0.34283 G=0.65717
gnomAD - Genomes African Sub 41998 A=0.19051 G=0.80949
gnomAD - Genomes American Sub 13632 A=0.38615 G=0.61385
gnomAD - Genomes Ashkenazi Jewish Sub 3320 A=0.3313 G=0.6687
gnomAD - Genomes East Asian Sub 3122 A=0.6855 G=0.3145
gnomAD - Genomes Other Sub 2152 A=0.3234 G=0.6766
The PAGE Study Global Study-wide 78470 A=0.35133 G=0.64867
The PAGE Study AfricanAmerican Sub 32438 A=0.19634 G=0.80366
The PAGE Study Mexican Sub 10786 A=0.46152 G=0.53848
The PAGE Study Asian Sub 8294 A=0.7005 G=0.2995
The PAGE Study PuertoRican Sub 7886 A=0.3060 G=0.6940
The PAGE Study NativeHawaiian Sub 4522 A=0.6325 G=0.3675
The PAGE Study Cuban Sub 4214 A=0.3393 G=0.6607
The PAGE Study Dominican Sub 3810 A=0.2570 G=0.7430
The PAGE Study CentralAmerican Sub 2438 A=0.4200 G=0.5800
The PAGE Study SouthAmerican Sub 1972 A=0.4574 G=0.5426
The PAGE Study NativeAmerican Sub 1258 A=0.3744 G=0.6256
The PAGE Study SouthAsian Sub 852 A=0.391 G=0.609
14KJPN JAPANESE Study-wide 28258 A=0.70886 G=0.29114
8.3KJPN JAPANESE Study-wide 16758 A=0.70969 G=0.29031
1000Genomes_30x Global Study-wide 6404 A=0.3857 G=0.6143
1000Genomes_30x African Sub 1786 A=0.1708 G=0.8292
1000Genomes_30x Europe Sub 1266 A=0.3420 G=0.6580
1000Genomes_30x South Asian Sub 1202 A=0.4027 G=0.5973
1000Genomes_30x East Asian Sub 1170 A=0.6915 G=0.3085
1000Genomes_30x American Sub 980 A=0.448 G=0.552
1000Genomes Global Study-wide 5008 A=0.3972 G=0.6028
1000Genomes African Sub 1322 A=0.1740 G=0.8260
1000Genomes East Asian Sub 1008 A=0.6994 G=0.3006
1000Genomes Europe Sub 1006 A=0.3449 G=0.6551
1000Genomes South Asian Sub 978 A=0.400 G=0.600
1000Genomes American Sub 694 A=0.455 G=0.545
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.3705 G=0.6295
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.3505 G=0.6495
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.3382 G=0.6618
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.7331 G=0.2669
HapMap Global Study-wide 1890 A=0.3508 G=0.6492
HapMap American Sub 768 A=0.440 G=0.560
HapMap African Sub 692 A=0.126 G=0.874
HapMap Asian Sub 254 A=0.732 G=0.268
HapMap Europe Sub 176 A=0.295 G=0.705
Korean Genome Project KOREAN Study-wide 1832 A=0.7069 G=0.2931
Genome-wide autozygosity in Daghestan Global Study-wide 1134 A=0.3677 G=0.6323
Genome-wide autozygosity in Daghestan Daghestan Sub 628 A=0.336 G=0.664
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.396 G=0.604
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.467 G=0.533
Genome-wide autozygosity in Daghestan Europe Sub 106 A=0.425 G=0.575
Genome-wide autozygosity in Daghestan South Asian Sub 98 A=0.40 G=0.60
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.22 G=0.78
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.323 G=0.677
CNV burdens in cranial meningiomas Global Study-wide 770 A=0.708 G=0.292
CNV burdens in cranial meningiomas CRM Sub 770 A=0.708 G=0.292
Northern Sweden ACPOP Study-wide 600 A=0.405 G=0.595
SGDP_PRJ Global Study-wide 424 A=0.318 G=0.682
Qatari Global Study-wide 216 A=0.352 G=0.648
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.659 G=0.341
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 60 A=0.63 G=0.37
Siberian Global Study-wide 46 A=0.33 G=0.67
The Danish reference pan genome Danish Study-wide 40 A=0.50 G=0.50
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 1 NC_000001.11:g.5067483A>G
GRCh37.p13 chr 1 NC_000001.10:g.5127543A>G
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= G
GRCh38.p14 chr 1 NC_000001.11:g.5067483= NC_000001.11:g.5067483A>G
GRCh37.p13 chr 1 NC_000001.10:g.5127543= NC_000001.10:g.5127543A>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#.

119 SubSNP, 24 Frequency submissions
No Submitter Submission ID Date (Build)
1 BCM_SSAHASNP ss9893869 Jul 11, 2003 (116)
2 WI_SSAHASNP ss11420230 Jul 11, 2003 (116)
3 SSAHASNP ss20476541 Apr 05, 2004 (121)
4 PERLEGEN ss46534264 Mar 14, 2006 (126)
5 AFFY ss66363978 Dec 01, 2006 (127)
6 AFFY ss76084891 Dec 08, 2007 (130)
7 HGSV ss81383403 Dec 15, 2007 (130)
8 KRIBB_YJKIM ss82277452 Dec 14, 2007 (130)
9 HGSV ss85059704 Dec 15, 2007 (130)
10 BCMHGSC_JDW ss87184748 Mar 23, 2008 (129)
11 HUMANGENOME_JCVI ss97916418 Feb 06, 2009 (130)
12 1000GENOMES ss107959223 Jan 22, 2009 (130)
13 1000GENOMES ss109987070 Jan 24, 2009 (130)
14 ILLUMINA-UK ss118463332 Feb 14, 2009 (130)
15 ENSEMBL ss138948591 Dec 01, 2009 (131)
16 ILLUMINA ss160791931 Dec 01, 2009 (131)
17 COMPLETE_GENOMICS ss163018051 Jul 04, 2010 (132)
18 COMPLETE_GENOMICS ss163757502 Jul 04, 2010 (132)
19 AFFY ss172449208 Jul 04, 2010 (132)
20 BUSHMAN ss197945455 Jul 04, 2010 (132)
21 BCM-HGSC-SUB ss205349036 Jul 04, 2010 (132)
22 1000GENOMES ss218210561 Jul 14, 2010 (132)
23 1000GENOMES ss230409818 Jul 14, 2010 (132)
24 1000GENOMES ss238127928 Jul 15, 2010 (132)
25 BL ss252888014 May 09, 2011 (134)
26 GMI ss275696601 May 04, 2012 (137)
27 GMI ss283993662 Apr 25, 2013 (138)
28 PJP ss290566998 May 09, 2011 (134)
29 ILLUMINA ss481298718 May 04, 2012 (137)
30 ILLUMINA ss481323541 May 04, 2012 (137)
31 ILLUMINA ss482306120 Sep 08, 2015 (146)
32 ILLUMINA ss485444592 May 04, 2012 (137)
33 ILLUMINA ss537370482 Sep 08, 2015 (146)
34 TISHKOFF ss553745320 Apr 25, 2013 (138)
35 SSMP ss647545236 Apr 25, 2013 (138)
36 ILLUMINA ss778945843 Aug 21, 2014 (142)
37 ILLUMINA ss783167749 Aug 21, 2014 (142)
38 ILLUMINA ss784123371 Aug 21, 2014 (142)
39 ILLUMINA ss832427226 Apr 01, 2015 (144)
40 ILLUMINA ss834407612 Aug 21, 2014 (142)
41 EVA-GONL ss974808775 Aug 21, 2014 (142)
42 JMKIDD_LAB ss1067636769 Aug 21, 2014 (142)
43 1000GENOMES ss1289495181 Aug 21, 2014 (142)
44 HAMMER_LAB ss1397238890 Sep 08, 2015 (146)
45 DDI ss1425697832 Apr 01, 2015 (144)
46 EVA_GENOME_DK ss1573865490 Apr 01, 2015 (144)
47 EVA_DECODE ss1584167490 Apr 01, 2015 (144)
48 EVA_UK10K_ALSPAC ss1599451447 Apr 01, 2015 (144)
49 EVA_UK10K_TWINSUK ss1642445480 Apr 01, 2015 (144)
50 EVA_SVP ss1712307881 Apr 01, 2015 (144)
51 ILLUMINA ss1751923413 Sep 08, 2015 (146)
52 HAMMER_LAB ss1793809438 Sep 08, 2015 (146)
53 WEILL_CORNELL_DGM ss1918005050 Feb 12, 2016 (147)
54 ILLUMINA ss1945983112 Feb 12, 2016 (147)
55 ILLUMINA ss1958235924 Feb 12, 2016 (147)
56 GENOMED ss1966674699 Jul 19, 2016 (147)
57 JJLAB ss2019519039 Sep 14, 2016 (149)
58 USC_VALOUEV ss2147510342 Dec 20, 2016 (150)
59 HUMAN_LONGEVITY ss2159662173 Dec 20, 2016 (150)
60 ILLUMINA ss2632470682 Nov 08, 2017 (151)
61 GRF ss2697405102 Nov 08, 2017 (151)
62 ILLUMINA ss2710664354 Nov 08, 2017 (151)
63 GNOMAD ss2751086888 Nov 08, 2017 (151)
64 SWEGEN ss2986219420 Nov 08, 2017 (151)
65 ILLUMINA ss3021048807 Nov 08, 2017 (151)
66 BIOINF_KMB_FNS_UNIBA ss3023523744 Nov 08, 2017 (151)
67 CSHL ss3343295567 Nov 08, 2017 (151)
68 ILLUMINA ss3625524154 Oct 11, 2018 (152)
69 ILLUMINA ss3626014914 Oct 11, 2018 (152)
70 ILLUMINA ss3630509826 Oct 11, 2018 (152)
71 ILLUMINA ss3632879107 Oct 11, 2018 (152)
72 ILLUMINA ss3633572780 Oct 11, 2018 (152)
73 ILLUMINA ss3634304150 Oct 11, 2018 (152)
74 ILLUMINA ss3635266940 Oct 11, 2018 (152)
75 ILLUMINA ss3635980525 Oct 11, 2018 (152)
76 ILLUMINA ss3637017300 Oct 11, 2018 (152)
77 ILLUMINA ss3640011515 Oct 11, 2018 (152)
78 ILLUMINA ss3644478968 Oct 11, 2018 (152)
79 URBANLAB ss3646589869 Oct 11, 2018 (152)
80 ILLUMINA ss3651371533 Oct 11, 2018 (152)
81 EGCUT_WGS ss3654320814 Jul 12, 2019 (153)
82 EVA_DECODE ss3686069858 Jul 12, 2019 (153)
83 ILLUMINA ss3724991878 Jul 12, 2019 (153)
84 ACPOP ss3726750734 Jul 12, 2019 (153)
85 ILLUMINA ss3744041282 Jul 12, 2019 (153)
86 ILLUMINA ss3744605137 Jul 12, 2019 (153)
87 EVA ss3745770799 Jul 12, 2019 (153)
88 PAGE_CC ss3770781702 Jul 12, 2019 (153)
89 ILLUMINA ss3772106791 Jul 12, 2019 (153)
90 PACBIO ss3783312292 Jul 12, 2019 (153)
91 PACBIO ss3788988975 Jul 12, 2019 (153)
92 PACBIO ss3793861623 Jul 12, 2019 (153)
93 KHV_HUMAN_GENOMES ss3798791743 Jul 12, 2019 (153)
94 EVA ss3826000647 Apr 25, 2020 (154)
95 EVA ss3836387552 Apr 25, 2020 (154)
96 EVA ss3841791770 Apr 25, 2020 (154)
97 SGDP_PRJ ss3848094408 Apr 25, 2020 (154)
98 KRGDB ss3892957674 Apr 25, 2020 (154)
99 KOGIC ss3943716546 Apr 25, 2020 (154)
100 EVA ss3984451377 Apr 25, 2021 (155)
101 EVA ss3984775888 Apr 25, 2021 (155)
102 EVA ss4016890815 Apr 25, 2021 (155)
103 TOPMED ss4437647994 Apr 25, 2021 (155)
104 TOMMO_GENOMICS ss5142250351 Apr 25, 2021 (155)
105 1000G_HIGH_COVERAGE ss5241006251 Oct 12, 2022 (156)
106 EVA ss5314589133 Oct 12, 2022 (156)
107 EVA ss5316443944 Oct 12, 2022 (156)
108 HUGCELL_USP ss5442227907 Oct 12, 2022 (156)
109 EVA ss5505755497 Oct 12, 2022 (156)
110 1000G_HIGH_COVERAGE ss5512689306 Oct 12, 2022 (156)
111 SANFORD_IMAGENETICS ss5624831088 Oct 12, 2022 (156)
112 TOMMO_GENOMICS ss5666478919 Oct 12, 2022 (156)
113 EVA ss5799473610 Oct 12, 2022 (156)
114 YY_MCH ss5800282515 Oct 12, 2022 (156)
115 EVA ss5831476024 Oct 12, 2022 (156)
116 EVA ss5847523279 Oct 12, 2022 (156)
117 EVA ss5848765170 Oct 12, 2022 (156)
118 EVA ss5906854938 Oct 12, 2022 (156)
119 EVA ss5936657148 Oct 12, 2022 (156)
120 1000Genomes NC_000001.10 - 5127543 Oct 11, 2018 (152)
121 1000Genomes_30x NC_000001.11 - 5067483 Oct 12, 2022 (156)
122 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 5127543 Oct 11, 2018 (152)
123 Genome-wide autozygosity in Daghestan NC_000001.9 - 5027403 Apr 25, 2020 (154)
124 Genetic variation in the Estonian population NC_000001.10 - 5127543 Oct 11, 2018 (152)
125 The Danish reference pan genome NC_000001.10 - 5127543 Apr 25, 2020 (154)
126 gnomAD - Genomes NC_000001.11 - 5067483 Apr 25, 2021 (155)
127 Genome of the Netherlands Release 5 NC_000001.10 - 5127543 Apr 25, 2020 (154)
128 HapMap NC_000001.11 - 5067483 Apr 25, 2020 (154)
129 KOREAN population from KRGDB NC_000001.10 - 5127543 Apr 25, 2020 (154)
130 Korean Genome Project NC_000001.11 - 5067483 Apr 25, 2020 (154)
131 Northern Sweden NC_000001.10 - 5127543 Jul 12, 2019 (153)
132 The PAGE Study NC_000001.11 - 5067483 Jul 12, 2019 (153)
133 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 5127543 Apr 25, 2021 (155)
134 CNV burdens in cranial meningiomas NC_000001.10 - 5127543 Apr 25, 2021 (155)
135 Qatari NC_000001.10 - 5127543 Apr 25, 2020 (154)
136 SGDP_PRJ NC_000001.10 - 5127543 Apr 25, 2020 (154)
137 Siberian NC_000001.10 - 5127543 Apr 25, 2020 (154)
138 8.3KJPN NC_000001.10 - 5127543 Apr 25, 2021 (155)
139 14KJPN NC_000001.11 - 5067483 Oct 12, 2022 (156)
140 TopMed NC_000001.11 - 5067483 Apr 25, 2021 (155)
141 UK 10K study - Twins NC_000001.10 - 5127543 Oct 11, 2018 (152)
142 A Vietnamese Genetic Variation Database NC_000001.10 - 5127543 Jul 12, 2019 (153)
143 ALFA NC_000001.11 - 5067483 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)
rs56539420 May 26, 2008 (130)
rs57448760 Feb 27, 2009 (130)
rs60904592 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss81383403, ss85059704 NC_000001.8:5037915:A:G NC_000001.11:5067482:A:G (self)
375, ss87184748, ss107959223, ss109987070, ss118463332, ss160791931, ss163018051, ss163757502, ss197945455, ss205349036, ss252888014, ss275696601, ss283993662, ss290566998, ss481298718, ss1397238890, ss1584167490, ss1712307881 NC_000001.9:5027402:A:G NC_000001.11:5067482:A:G (self)
164552, 79701, 59062, 1372724, 35127, 135068, 35599, 1815, 677, 46980, 111388, 26696, 219658, 79701, 17847, ss218210561, ss230409818, ss238127928, ss481323541, ss482306120, ss485444592, ss537370482, ss553745320, ss647545236, ss778945843, ss783167749, ss784123371, ss832427226, ss834407612, ss974808775, ss1067636769, ss1289495181, ss1425697832, ss1573865490, ss1599451447, ss1642445480, ss1751923413, ss1793809438, ss1918005050, ss1945983112, ss1958235924, ss1966674699, ss2019519039, ss2147510342, ss2632470682, ss2697405102, ss2710664354, ss2751086888, ss2986219420, ss3021048807, ss3343295567, ss3625524154, ss3626014914, ss3630509826, ss3632879107, ss3633572780, ss3634304150, ss3635266940, ss3635980525, ss3637017300, ss3640011515, ss3644478968, ss3651371533, ss3654320814, ss3726750734, ss3744041282, ss3744605137, ss3745770799, ss3772106791, ss3783312292, ss3788988975, ss3793861623, ss3826000647, ss3836387552, ss3848094408, ss3892957674, ss3984451377, ss3984775888, ss4016890815, ss5142250351, ss5314589133, ss5316443944, ss5505755497, ss5624831088, ss5799473610, ss5831476024, ss5847523279, ss5936657148 NC_000001.10:5127542:A:G NC_000001.11:5067482:A:G (self)
215241, 1150667, 5561, 94547, 3171, 316023, 1254329, 11983174093, ss2159662173, ss3023523744, ss3646589869, ss3686069858, ss3724991878, ss3770781702, ss3798791743, ss3841791770, ss3943716546, ss4437647994, ss5241006251, ss5442227907, ss5512689306, ss5666478919, ss5800282515, ss5848765170, ss5906854938 NC_000001.11:5067482:A:G NC_000001.11:5067482:A:G (self)
ss20476541 NT_004547.16:1131175:A:G NC_000001.11:5067482:A:G (self)
ss46534264, ss66363978, ss76084891, ss82277452, ss97916418, ss138948591, ss172449208 NT_021937.19:1132274:A:G NC_000001.11:5067482:A:G (self)
ss9893869, ss11420230 NT_077917.1:49042:A:G NC_000001.11:5067482:A: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 rs6603832

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