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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.

rs1000016

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:234782338 (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 / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.087905 (26075/296628, ALFA)
G=0.088689 (23475/264690, TOPMED)
G=0.093224 (19118/205076, GENOGRAPHIC) (+ 25 more)
G=0.071643 (10040/140140, GnomAD)
G=0.14403 (11335/78700, PAGE_STUDY)
G=0.47735 (13488/28256, 14KJPN)
G=0.47076 (7890/16760, 8.3KJPN)
G=0.1722 (1103/6404, 1000G_30x)
G=0.1809 (906/5008, 1000G)
G=0.0493 (221/4480, Estonian)
G=0.0719 (277/3854, ALSPAC)
G=0.0709 (263/3708, TWINSUK)
G=0.4253 (1246/2930, KOREAN)
G=0.2241 (467/2084, HGDP_Stanford)
G=0.4050 (742/1832, Korea1K)
G=0.1677 (283/1688, HapMap)
G=0.1558 (177/1136, Daghestan)
G=0.061 (61/998, GoNL)
G=0.452 (357/790, PRJEB37584)
G=0.047 (28/600, NorthernSweden)
G=0.148 (32/216, Qatari)
A=0.375 (81/216, SGDP_PRJ)
A=0.500 (107/214, Vietnamese)
G=0.500 (107/214, Vietnamese)
G=0.12 (8/64, Ancient Sardinia)
G=0.20 (8/40, GENOME_DK)
A=0.5 (5/10, Siberian)
G=0.5 (5/10, Siberian)
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 301664 A=0.912515 G=0.087485
European Sub 268936 A=0.921457 G=0.078543
African Sub 9522 A=0.9823 G=0.0177
African Others Sub 372 A=1.000 G=0.000
African American Sub 9150 A=0.9815 G=0.0185
Asian Sub 3936 A=0.5127 G=0.4873
East Asian Sub 3190 A=0.5408 G=0.4592
Other Asian Sub 746 A=0.393 G=0.607
Latin American 1 Sub 1074 A=0.8957 G=0.1043
Latin American 2 Sub 3158 A=0.8255 G=0.1745
South Asian Sub 5224 A=0.7940 G=0.2060
Other Sub 9814 A=0.8531 G=0.1469


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
Allele Frequency Aggregator Total Global 296628 A=0.912095 G=0.087905
Allele Frequency Aggregator European Sub 265842 A=0.921235 G=0.078765
Allele Frequency Aggregator Other Sub 9014 A=0.8526 G=0.1474
Allele Frequency Aggregator African Sub 8380 A=0.9821 G=0.0179
Allele Frequency Aggregator South Asian Sub 5224 A=0.7940 G=0.2060
Allele Frequency Aggregator Asian Sub 3936 A=0.5127 G=0.4873
Allele Frequency Aggregator Latin American 2 Sub 3158 A=0.8255 G=0.1745
Allele Frequency Aggregator Latin American 1 Sub 1074 A=0.8957 G=0.1043
TopMed Global Study-wide 264690 A=0.911311 G=0.088689
Genographic Project Global Study-wide 205076 A=0.906776 G=0.093224
gnomAD - Genomes Global Study-wide 140140 A=0.928357 G=0.071643
gnomAD - Genomes European Sub 75920 A=0.93292 G=0.06708
gnomAD - Genomes African Sub 41984 A=0.98073 G=0.01927
gnomAD - Genomes American Sub 13642 A=0.86600 G=0.13400
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=0.8462 G=0.1538
gnomAD - Genomes East Asian Sub 3118 A=0.4933 G=0.5067
gnomAD - Genomes Other Sub 2154 A=0.8983 G=0.1017
The PAGE Study Global Study-wide 78700 A=0.85597 G=0.14403
The PAGE Study AfricanAmerican Sub 32514 A=0.97804 G=0.02196
The PAGE Study Mexican Sub 10810 A=0.79500 G=0.20500
The PAGE Study Asian Sub 8318 A=0.5154 G=0.4846
The PAGE Study PuertoRican Sub 7918 A=0.9196 G=0.0804
The PAGE Study NativeHawaiian Sub 4534 A=0.5254 G=0.4746
The PAGE Study Cuban Sub 4230 A=0.9137 G=0.0863
The PAGE Study Dominican Sub 3828 A=0.9360 G=0.0640
The PAGE Study CentralAmerican Sub 2450 A=0.8661 G=0.1339
The PAGE Study SouthAmerican Sub 1982 A=0.8481 G=0.1519
The PAGE Study NativeAmerican Sub 1260 A=0.8786 G=0.1214
The PAGE Study SouthAsian Sub 856 A=0.775 G=0.225
14KJPN JAPANESE Study-wide 28256 A=0.52265 G=0.47735
8.3KJPN JAPANESE Study-wide 16760 A=0.52924 G=0.47076
1000Genomes_30x Global Study-wide 6404 A=0.8278 G=0.1722
1000Genomes_30x African Sub 1786 A=0.9938 G=0.0062
1000Genomes_30x Europe Sub 1266 A=0.9171 G=0.0829
1000Genomes_30x South Asian Sub 1202 A=0.7629 G=0.2371
1000Genomes_30x East Asian Sub 1170 A=0.5000 G=0.5000
1000Genomes_30x American Sub 980 A=0.881 G=0.119
1000Genomes Global Study-wide 5008 A=0.8191 G=0.1809
1000Genomes African Sub 1322 A=0.9939 G=0.0061
1000Genomes East Asian Sub 1008 A=0.5050 G=0.4950
1000Genomes Europe Sub 1006 A=0.9185 G=0.0815
1000Genomes South Asian Sub 978 A=0.764 G=0.236
1000Genomes American Sub 694 A=0.876 G=0.124
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.9507 G=0.0493
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.9281 G=0.0719
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.9291 G=0.0709
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.5747 G=0.4253, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2084 A=0.7759 G=0.2241
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.532 G=0.468
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.783 G=0.217
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.829 G=0.171
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.900 G=0.100
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.992 G=0.008
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.764 G=0.236
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.83 G=0.17
Korean Genome Project KOREAN Study-wide 1832 A=0.5950 G=0.4050
HapMap Global Study-wide 1688 A=0.8323 G=0.1677
HapMap American Sub 672 A=0.804 G=0.196
HapMap African Sub 586 A=0.971 G=0.029
HapMap Asian Sub 254 A=0.531 G=0.469
HapMap Europe Sub 176 A=0.915 G=0.085
Genome-wide autozygosity in Daghestan Global Study-wide 1136 A=0.8442 G=0.1558
Genome-wide autozygosity in Daghestan Daghestan Sub 628 A=0.850 G=0.150
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.868 G=0.132
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.787 G=0.213
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.907 G=0.093
Genome-wide autozygosity in Daghestan South Asian Sub 98 A=0.77 G=0.23
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.86 G=0.14
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.939 G=0.061
CNV burdens in cranial meningiomas Global Study-wide 790 A=0.548 G=0.452
CNV burdens in cranial meningiomas CRM Sub 790 A=0.548 G=0.452
Northern Sweden ACPOP Study-wide 600 A=0.953 G=0.047
Qatari Global Study-wide 216 A=0.852 G=0.148
SGDP_PRJ Global Study-wide 216 A=0.375 G=0.625
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.500 G=0.500
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 64 A=0.88 G=0.12
The Danish reference pan genome Danish Study-wide 40 A=0.80 G=0.20
Siberian Global Study-wide 10 A=0.5 G=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 2 NC_000002.12:g.234782338A>G
GRCh38.p14 chr 2 NC_000002.12:g.234782338A>T
GRCh37.p13 chr 2 NC_000002.11:g.235690982A>G
GRCh37.p13 chr 2 NC_000002.11:g.235690982A>T
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 T
GRCh38.p14 chr 2 NC_000002.12:g.234782338= NC_000002.12:g.234782338A>G NC_000002.12:g.234782338A>T
GRCh37.p13 chr 2 NC_000002.11:g.235690982= NC_000002.11:g.235690982A>G NC_000002.11:g.235690982A>T
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#.

118 SubSNP, 26 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1459594 Oct 05, 2000 (86)
2 CSHL-HAPMAP ss19460565 Feb 27, 2004 (120)
3 PERLEGEN ss23873528 Sep 20, 2004 (123)
4 ABI ss44267866 Mar 15, 2006 (126)
5 ILLUMINA ss66568853 Dec 01, 2006 (127)
6 ILLUMINA ss66863613 Dec 01, 2006 (127)
7 ILLUMINA ss66932318 Dec 01, 2006 (127)
8 ILLUMINA ss70355784 May 17, 2007 (127)
9 ILLUMINA ss70458960 May 23, 2008 (130)
10 ILLUMINA ss70979502 May 17, 2007 (127)
11 ILLUMINA ss75710002 Dec 06, 2007 (129)
12 KRIBB_YJKIM ss83650139 Dec 14, 2007 (130)
13 BGI ss106169484 Feb 04, 2009 (130)
14 ILLUMINA ss121251260 Dec 01, 2009 (131)
15 ILLUMINA ss152537366 Dec 01, 2009 (131)
16 ILLUMINA ss159102813 Dec 01, 2009 (131)
17 ILLUMINA ss159849746 Dec 01, 2009 (131)
18 ENSEMBL ss161246189 Dec 01, 2009 (131)
19 ILLUMINA ss169203223 Jul 04, 2010 (132)
20 ILLUMINA ss169483908 Jul 04, 2010 (132)
21 1000GENOMES ss231639529 Jul 14, 2010 (132)
22 1000GENOMES ss239086365 Jul 15, 2010 (132)
23 GMI ss276947871 May 04, 2012 (137)
24 ILLUMINA ss479152954 May 04, 2012 (137)
25 ILLUMINA ss479153673 May 04, 2012 (137)
26 ILLUMINA ss479465651 Sep 08, 2015 (146)
27 ILLUMINA ss484377076 May 04, 2012 (137)
28 ILLUMINA ss536563755 Sep 08, 2015 (146)
29 TISHKOFF ss556311863 Apr 25, 2013 (138)
30 SSMP ss649972447 Apr 25, 2013 (138)
31 ILLUMINA ss778719118 Sep 08, 2015 (146)
32 ILLUMINA ss782634834 Sep 08, 2015 (146)
33 ILLUMINA ss783604391 Sep 08, 2015 (146)
34 ILLUMINA ss825325515 Jul 19, 2016 (147)
35 ILLUMINA ss831884896 Sep 08, 2015 (146)
36 ILLUMINA ss832615609 Jul 13, 2019 (153)
37 ILLUMINA ss834178495 Sep 08, 2015 (146)
38 EVA-GONL ss978097989 Aug 21, 2014 (142)
39 JMKIDD_LAB ss1070043173 Aug 21, 2014 (142)
40 1000GENOMES ss1302167190 Aug 21, 2014 (142)
41 HAMMER_LAB ss1397324243 Sep 08, 2015 (146)
42 DDI ss1428953155 Apr 01, 2015 (144)
43 EVA_GENOME_DK ss1579377547 Apr 01, 2015 (144)
44 EVA_DECODE ss1587558314 Apr 01, 2015 (144)
45 EVA_UK10K_ALSPAC ss1606075972 Apr 01, 2015 (144)
46 EVA_UK10K_TWINSUK ss1649070005 Apr 01, 2015 (144)
47 EVA_SVP ss1712540835 Apr 01, 2015 (144)
48 ILLUMINA ss1752345845 Sep 08, 2015 (146)
49 WEILL_CORNELL_DGM ss1921345910 Feb 12, 2016 (147)
50 ILLUMINA ss1946070306 Feb 12, 2016 (147)
51 ILLUMINA ss1958520288 Feb 12, 2016 (147)
52 GENOMED ss1969058014 Jul 19, 2016 (147)
53 JJLAB ss2021221606 Sep 14, 2016 (149)
54 USC_VALOUEV ss2149288005 Dec 20, 2016 (150)
55 HUMAN_LONGEVITY ss2240226489 Dec 20, 2016 (150)
56 SYSTEMSBIOZJU ss2625111275 Nov 08, 2017 (151)
57 ILLUMINA ss2633756917 Nov 08, 2017 (151)
58 GRF ss2703940902 Nov 08, 2017 (151)
59 ILLUMINA ss2710929285 Nov 08, 2017 (151)
60 GNOMAD ss2787798109 Nov 08, 2017 (151)
61 SWEGEN ss2991572050 Nov 08, 2017 (151)
62 ILLUMINA ss3022084776 Nov 08, 2017 (151)
63 BIOINF_KMB_FNS_UNIBA ss3024371113 Nov 08, 2017 (151)
64 CSHL ss3344803222 Nov 08, 2017 (151)
65 ILLUMINA ss3625780051 Oct 11, 2018 (152)
66 ILLUMINA ss3628316503 Oct 11, 2018 (152)
67 ILLUMINA ss3631716034 Oct 11, 2018 (152)
68 ILLUMINA ss3633239046 Oct 11, 2018 (152)
69 ILLUMINA ss3633952458 Oct 11, 2018 (152)
70 ILLUMINA ss3634818813 Oct 11, 2018 (152)
71 ILLUMINA ss3635637798 Oct 11, 2018 (152)
72 ILLUMINA ss3636508960 Oct 11, 2018 (152)
73 ILLUMINA ss3637389838 Oct 11, 2018 (152)
74 ILLUMINA ss3638326338 Oct 11, 2018 (152)
75 ILLUMINA ss3639166540 Oct 11, 2018 (152)
76 ILLUMINA ss3639597013 Oct 11, 2018 (152)
77 ILLUMINA ss3640526112 Oct 11, 2018 (152)
78 ILLUMINA ss3641122608 Oct 11, 2018 (152)
79 ILLUMINA ss3641418754 Oct 11, 2018 (152)
80 ILLUMINA ss3643290485 Oct 11, 2018 (152)
81 ILLUMINA ss3644773012 Oct 11, 2018 (152)
82 ILLUMINA ss3652537642 Oct 11, 2018 (152)
83 EGCUT_WGS ss3659469852 Jul 13, 2019 (153)
84 EVA_DECODE ss3706283197 Jul 13, 2019 (153)
85 ILLUMINA ss3725886338 Jul 13, 2019 (153)
86 ACPOP ss3729489391 Jul 13, 2019 (153)
87 ILLUMINA ss3744192670 Jul 13, 2019 (153)
88 ILLUMINA ss3745118697 Jul 13, 2019 (153)
89 EVA ss3758245690 Jul 13, 2019 (153)
90 PAGE_CC ss3770997711 Jul 13, 2019 (153)
91 ILLUMINA ss3772615070 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3802608054 Jul 13, 2019 (153)
93 EVA ss3827574711 Apr 25, 2020 (154)
94 HGDP ss3847655500 Apr 25, 2020 (154)
95 SGDP_PRJ ss3854871884 Apr 25, 2020 (154)
96 KRGDB ss3900622545 Apr 25, 2020 (154)
97 KOGIC ss3950352437 Apr 25, 2020 (154)
98 EVA ss3984500158 Apr 26, 2021 (155)
99 EVA ss3984962260 Apr 26, 2021 (155)
100 EVA ss4017056402 Apr 26, 2021 (155)
101 TOPMED ss4549089321 Apr 26, 2021 (155)
102 TOMMO_GENOMICS ss5157091958 Apr 26, 2021 (155)
103 1000G_HIGH_COVERAGE ss5252491792 Oct 12, 2022 (156)
104 GENOGRAPHIC ss5314487272 Oct 12, 2022 (156)
105 EVA ss5314818589 Oct 12, 2022 (156)
106 EVA ss5336875555 Oct 12, 2022 (156)
107 HUGCELL_USP ss5452056919 Oct 12, 2022 (156)
108 EVA ss5506839743 Oct 12, 2022 (156)
109 1000G_HIGH_COVERAGE ss5530060427 Oct 12, 2022 (156)
110 SANFORD_IMAGENETICS ss5631214879 Oct 12, 2022 (156)
111 TOMMO_GENOMICS ss5688153898 Oct 12, 2022 (156)
112 EVA ss5799564253 Oct 12, 2022 (156)
113 YY_MCH ss5803335766 Oct 12, 2022 (156)
114 EVA ss5821772168 Oct 12, 2022 (156)
115 EVA ss5847908391 Oct 12, 2022 (156)
116 EVA ss5853005851 Oct 12, 2022 (156)
117 EVA ss5935234298 Oct 12, 2022 (156)
118 EVA ss5957481558 Oct 12, 2022 (156)
119 1000Genomes NC_000002.11 - 235690982 Oct 11, 2018 (152)
120 1000Genomes_30x NC_000002.12 - 234782338 Oct 12, 2022 (156)
121 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 235690982 Oct 11, 2018 (152)
122 Genome-wide autozygosity in Daghestan NC_000002.10 - 235355721 Apr 25, 2020 (154)
123 Genetic variation in the Estonian population NC_000002.11 - 235690982 Oct 11, 2018 (152)
124 Genographic Project NC_000002.12 - 234782338 Oct 12, 2022 (156)
125 The Danish reference pan genome NC_000002.11 - 235690982 Apr 25, 2020 (154)
126 gnomAD - Genomes NC_000002.12 - 234782338 Apr 26, 2021 (155)
127 Genome of the Netherlands Release 5 NC_000002.11 - 235690982 Apr 25, 2020 (154)
128 HGDP-CEPH-db Supplement 1 NC_000002.10 - 235355721 Apr 25, 2020 (154)
129 HapMap NC_000002.12 - 234782338 Apr 25, 2020 (154)
130 KOREAN population from KRGDB NC_000002.11 - 235690982 Apr 25, 2020 (154)
131 Korean Genome Project NC_000002.12 - 234782338 Apr 25, 2020 (154)
132 Northern Sweden NC_000002.11 - 235690982 Jul 13, 2019 (153)
133 The PAGE Study NC_000002.12 - 234782338 Jul 13, 2019 (153)
134 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000002.11 - 235690982 Apr 26, 2021 (155)
135 CNV burdens in cranial meningiomas NC_000002.11 - 235690982 Apr 26, 2021 (155)
136 Qatari NC_000002.11 - 235690982 Apr 25, 2020 (154)
137 SGDP_PRJ NC_000002.11 - 235690982 Apr 25, 2020 (154)
138 Siberian NC_000002.11 - 235690982 Apr 25, 2020 (154)
139 8.3KJPN NC_000002.11 - 235690982 Apr 26, 2021 (155)
140 14KJPN NC_000002.12 - 234782338 Oct 12, 2022 (156)
141 TopMed NC_000002.12 - 234782338 Apr 26, 2021 (155)
142 UK 10K study - Twins NC_000002.11 - 235690982 Oct 11, 2018 (152)
143 A Vietnamese Genetic Variation Database NC_000002.11 - 235690982 Jul 13, 2019 (153)
144 ALFA NC_000002.12 - 234782338 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)
rs57575329 May 23, 2008 (130)
rs386508640 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss3639166540, ss3639597013 NC_000002.9:235472981:A:G NC_000002.12:234782337:A:G (self)
273967, 333392, ss276947871, ss479152954, ss825325515, ss1397324243, ss1587558314, ss1712540835, ss3643290485, ss3847655500 NC_000002.10:235355720:A:G NC_000002.12:234782337:A:G (self)
13291414, 7362954, 5208100, 5542486, 3226298, 7799939, 2774256, 188187, 49498, 3387840, 6888864, 1804359, 15061265, 7362954, 1599048, ss231639529, ss239086365, ss479153673, ss479465651, ss484377076, ss536563755, ss556311863, ss649972447, ss778719118, ss782634834, ss783604391, ss831884896, ss832615609, ss834178495, ss978097989, ss1070043173, ss1302167190, ss1428953155, ss1579377547, ss1606075972, ss1649070005, ss1752345845, ss1921345910, ss1946070306, ss1958520288, ss1969058014, ss2021221606, ss2149288005, ss2625111275, ss2633756917, ss2703940902, ss2710929285, ss2787798109, ss2991572050, ss3022084776, ss3344803222, ss3625780051, ss3628316503, ss3631716034, ss3633239046, ss3633952458, ss3634818813, ss3635637798, ss3636508960, ss3637389838, ss3638326338, ss3640526112, ss3641122608, ss3641418754, ss3644773012, ss3652537642, ss3659469852, ss3729489391, ss3744192670, ss3745118697, ss3758245690, ss3772615070, ss3827574711, ss3854871884, ss3900622545, ss3984500158, ss3984962260, ss4017056402, ss5157091958, ss5314818589, ss5336875555, ss5506839743, ss5631214879, ss5799564253, ss5821772168, ss5847908391, ss5957481558 NC_000002.11:235690981:A:G NC_000002.12:234782337:A:G (self)
17586362, 87172, 94677883, 2037944, 6730438, 219180, 21991002, 352912200, 9483444520, ss2240226489, ss3024371113, ss3706283197, ss3725886338, ss3770997711, ss3802608054, ss3950352437, ss4549089321, ss5252491792, ss5314487272, ss5452056919, ss5530060427, ss5688153898, ss5803335766, ss5853005851, ss5935234298 NC_000002.12:234782337:A:G NC_000002.12:234782337:A:G (self)
ss19460565 NT_005120.14:1621451:A:G NC_000002.12:234782337:A:G (self)
ss1459594, ss23873528, ss44267866, ss66568853, ss66863613, ss66932318, ss70355784, ss70458960, ss70979502, ss75710002, ss83650139, ss106169484, ss121251260, ss152537366, ss159102813, ss159849746, ss161246189, ss169203223, ss169483908 NT_005120.16:1637240:A:G NC_000002.12:234782337:A:G (self)
7799939, ss3900622545 NC_000002.11:235690981:A:T NC_000002.12:234782337:A:T (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 rs1000016

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