Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

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.

rs12714263

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:29095211 (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=0.433220 (114669/264690, TOPMED)
G=0.434961 (80058/184058, ALFA)
G=0.438696 (61363/139876, GnomAD) (+ 20 more)
G=0.12149 (3433/28258, 14KJPN)
G=0.12232 (2050/16760, 8.3KJPN)
G=0.3620 (2318/6404, 1000G_30x)
G=0.3572 (1789/5008, 1000G)
G=0.4321 (1936/4480, Estonian)
G=0.4302 (1658/3854, ALSPAC)
G=0.4404 (1633/3708, TWINSUK)
G=0.1522 (446/2930, KOREAN)
G=0.3385 (704/2080, HGDP_Stanford)
G=0.3671 (693/1888, HapMap)
G=0.1474 (270/1832, Korea1K)
G=0.4653 (523/1124, Daghestan)
G=0.428 (427/998, GoNL)
G=0.492 (295/600, NorthernSweden)
G=0.002 (1/534, MGP)
A=0.392 (102/260, SGDP_PRJ)
G=0.458 (99/216, Qatari)
G=0.28 (22/78, Ancient Sardinia)
G=0.40 (16/40, GENOME_DK)
A=0.36 (10/28, Siberian)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
LOC105374386 : Intron Variant
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 184058 A=0.565039 G=0.434961, T=0.000000
European Sub 164982 A=0.561473 G=0.438527, T=0.000000
African Sub 6034 A=0.4738 G=0.5262, T=0.0000
African Others Sub 238 A=0.504 G=0.496, T=0.000
African American Sub 5796 A=0.4726 G=0.5274, T=0.0000
Asian Sub 392 A=0.890 G=0.110, T=0.000
East Asian Sub 282 A=0.879 G=0.121, T=0.000
Other Asian Sub 110 A=0.918 G=0.082, T=0.000
Latin American 1 Sub 736 A=0.560 G=0.440, T=0.000
Latin American 2 Sub 2638 A=0.7282 G=0.2718, T=0.0000
South Asian Sub 5006 A=0.6516 G=0.3484, T=0.0000
Other Sub 4270 A=0.6005 G=0.3995, T=0.0000


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=0.566780 G=0.433220
Allele Frequency Aggregator Total Global 184058 A=0.565039 G=0.434961, T=0.000000
Allele Frequency Aggregator European Sub 164982 A=0.561473 G=0.438527, T=0.000000
Allele Frequency Aggregator African Sub 6034 A=0.4738 G=0.5262, T=0.0000
Allele Frequency Aggregator South Asian Sub 5006 A=0.6516 G=0.3484, T=0.0000
Allele Frequency Aggregator Other Sub 4270 A=0.6005 G=0.3995, T=0.0000
Allele Frequency Aggregator Latin American 2 Sub 2638 A=0.7282 G=0.2718, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 736 A=0.560 G=0.440, T=0.000
Allele Frequency Aggregator Asian Sub 392 A=0.890 G=0.110, T=0.000
gnomAD - Genomes Global Study-wide 139876 A=0.561304 G=0.438696
gnomAD - Genomes European Sub 75788 A=0.57860 G=0.42140
gnomAD - Genomes African Sub 41878 A=0.47175 G=0.52825
gnomAD - Genomes American Sub 13622 A=0.68110 G=0.31890
gnomAD - Genomes Ashkenazi Jewish Sub 3318 A=0.4795 G=0.5205
gnomAD - Genomes East Asian Sub 3124 A=0.8947 G=0.1053
gnomAD - Genomes Other Sub 2146 A=0.5788 G=0.4212
14KJPN JAPANESE Study-wide 28258 A=0.87851 G=0.12149
8.3KJPN JAPANESE Study-wide 16760 A=0.87768 G=0.12232
1000Genomes_30x Global Study-wide 6404 A=0.6380 G=0.3620
1000Genomes_30x African Sub 1786 A=0.4468 G=0.5532
1000Genomes_30x Europe Sub 1266 A=0.6051 G=0.3949
1000Genomes_30x South Asian Sub 1202 A=0.6847 G=0.3153
1000Genomes_30x East Asian Sub 1170 A=0.8829 G=0.1171
1000Genomes_30x American Sub 980 A=0.680 G=0.320
1000Genomes Global Study-wide 5008 A=0.6428 G=0.3572
1000Genomes African Sub 1322 A=0.4486 G=0.5514
1000Genomes East Asian Sub 1008 A=0.8760 G=0.1240
1000Genomes Europe Sub 1006 A=0.6044 G=0.3956
1000Genomes South Asian Sub 978 A=0.683 G=0.317
1000Genomes American Sub 694 A=0.673 G=0.327
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.5679 G=0.4321
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.5698 G=0.4302
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.5596 G=0.4404
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.8478 G=0.1522, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2080 A=0.6615 G=0.3385
HGDP-CEPH-db Supplement 1 Est_Asia Sub 468 A=0.844 G=0.156
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.614 G=0.386
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.526 G=0.474
HGDP-CEPH-db Supplement 1 Europe Sub 318 A=0.575 G=0.425
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.364 G=0.636
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.944 G=0.056
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.94 G=0.06
HapMap Global Study-wide 1888 A=0.6329 G=0.3671
HapMap American Sub 768 A=0.669 G=0.331
HapMap African Sub 690 A=0.528 G=0.472
HapMap Asian Sub 254 A=0.874 G=0.126
HapMap Europe Sub 176 A=0.540 G=0.460
Korean Genome Project KOREAN Study-wide 1832 A=0.8526 G=0.1474
Genome-wide autozygosity in Daghestan Global Study-wide 1124 A=0.5347 G=0.4653
Genome-wide autozygosity in Daghestan Daghestan Sub 624 A=0.463 G=0.537
Genome-wide autozygosity in Daghestan Near_East Sub 144 A=0.562 G=0.438
Genome-wide autozygosity in Daghestan Central Asia Sub 122 A=0.680 G=0.320
Genome-wide autozygosity in Daghestan Europe Sub 108 A=0.593 G=0.407
Genome-wide autozygosity in Daghestan South Asian Sub 90 A=0.70 G=0.30
Genome-wide autozygosity in Daghestan Caucasus Sub 36 A=0.58 G=0.42
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.572 G=0.428
Northern Sweden ACPOP Study-wide 600 A=0.508 G=0.492
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 A=0.998 G=0.002
SGDP_PRJ Global Study-wide 260 A=0.392 G=0.608
Qatari Global Study-wide 216 A=0.542 G=0.458
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 78 A=0.72 G=0.28
The Danish reference pan genome Danish Study-wide 40 A=0.60 G=0.40
Siberian Global Study-wide 28 A=0.36 G=0.64
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.29095211A>G
GRCh38.p14 chr 2 NC_000002.12:g.29095211A>T
GRCh37.p13 chr 2 NC_000002.11:g.29318077A>G
GRCh37.p13 chr 2 NC_000002.11:g.29318077A>T
Gene: LOC105374386, uncharacterized LOC105374386 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
LOC105374386 transcript variant X2 XR_007086265.1:n. N/A Intron Variant
LOC105374386 transcript variant X1 XR_939903.3:n. N/A Genic Upstream 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
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.29095211= NC_000002.12:g.29095211A>G NC_000002.12:g.29095211A>T
GRCh37.p13 chr 2 NC_000002.11:g.29318077= NC_000002.11:g.29318077A>G NC_000002.11:g.29318077A>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#.

114 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 SSAHASNP ss21635612 Apr 05, 2004 (121)
2 WUGSC_SSAHASNP ss23093828 Apr 05, 2004 (121)
3 ABI ss41587378 Mar 15, 2006 (126)
4 ILLUMINA ss67035704 Dec 01, 2006 (127)
5 ILLUMINA ss67359519 Dec 01, 2006 (127)
6 ILLUMINA ss68137768 Dec 12, 2006 (127)
7 PERLEGEN ss68807827 May 17, 2007 (127)
8 ILLUMINA ss70582927 May 26, 2008 (130)
9 ILLUMINA ss71125443 May 17, 2007 (127)
10 ILLUMINA ss75568241 Dec 06, 2007 (129)
11 HGSV ss84677094 Dec 15, 2007 (130)
12 KRIBB_YJKIM ss85267046 Dec 15, 2007 (130)
13 BCMHGSC_JDW ss91100164 Mar 24, 2008 (129)
14 1000GENOMES ss109359179 Jan 24, 2009 (130)
15 1000GENOMES ss110000735 Jan 24, 2009 (130)
16 ILLUMINA-UK ss117636427 Feb 14, 2009 (130)
17 ENSEMBL ss135907155 Dec 01, 2009 (131)
18 ILLUMINA ss153274163 Dec 01, 2009 (131)
19 GMI ss156844000 Dec 01, 2009 (131)
20 ILLUMINA ss159232647 Dec 01, 2009 (131)
21 ILLUMINA ss160296589 Dec 01, 2009 (131)
22 COMPLETE_GENOMICS ss163231529 Jul 04, 2010 (132)
23 ILLUMINA ss172231091 Jul 04, 2010 (132)
24 BUSHMAN ss200205807 Jul 04, 2010 (132)
25 1000GENOMES ss219139481 Jul 14, 2010 (132)
26 1000GENOMES ss231090292 Jul 14, 2010 (132)
27 1000GENOMES ss238662840 Jul 15, 2010 (132)
28 GMI ss276398312 May 04, 2012 (137)
29 GMI ss284314559 Apr 25, 2013 (138)
30 PJP ss292534034 May 09, 2011 (134)
31 ILLUMINA ss479811559 May 04, 2012 (137)
32 ILLUMINA ss479818670 May 04, 2012 (137)
33 ILLUMINA ss480403156 Sep 08, 2015 (146)
34 ILLUMINA ss484704278 May 04, 2012 (137)
35 ILLUMINA ss536810448 Sep 08, 2015 (146)
36 TISHKOFF ss555439564 Apr 25, 2013 (138)
37 SSMP ss649019950 Apr 25, 2013 (138)
38 ILLUMINA ss778789318 Sep 08, 2015 (146)
39 ILLUMINA ss782798906 Sep 08, 2015 (146)
40 ILLUMINA ss783764468 Sep 08, 2015 (146)
41 ILLUMINA ss832051850 Sep 08, 2015 (146)
42 ILLUMINA ss832744985 Jul 13, 2019 (153)
43 ILLUMINA ss834249348 Sep 08, 2015 (146)
44 EVA-GONL ss976625811 Aug 21, 2014 (142)
45 JMKIDD_LAB ss1068960502 Aug 21, 2014 (142)
46 1000GENOMES ss1296440931 Aug 21, 2014 (142)
47 HAMMER_LAB ss1397286118 Sep 08, 2015 (146)
48 DDI ss1428517556 Apr 01, 2015 (144)
49 EVA_GENOME_DK ss1578794758 Apr 01, 2015 (144)
50 EVA_DECODE ss1586031492 Apr 01, 2015 (144)
51 EVA_UK10K_ALSPAC ss1603091996 Apr 01, 2015 (144)
52 EVA_UK10K_TWINSUK ss1646086029 Apr 01, 2015 (144)
53 EVA_MGP ss1710958373 Apr 01, 2015 (144)
54 EVA_SVP ss1712440948 Apr 01, 2015 (144)
55 ILLUMINA ss1752351442 Sep 08, 2015 (146)
56 HAMMER_LAB ss1796469809 Sep 08, 2015 (146)
57 WEILL_CORNELL_DGM ss1919858028 Feb 12, 2016 (147)
58 GENOMED ss1968724126 Jul 19, 2016 (147)
59 JJLAB ss2020457500 Sep 14, 2016 (149)
60 USC_VALOUEV ss2148502201 Dec 20, 2016 (150)
61 HUMAN_LONGEVITY ss2228623584 Dec 20, 2016 (150)
62 ILLUMINA ss2633588967 Nov 08, 2017 (151)
63 ILLUMINA ss2635087462 Nov 08, 2017 (151)
64 GRF ss2703063240 Nov 08, 2017 (151)
65 GNOMAD ss2771230299 Nov 08, 2017 (151)
66 SWEGEN ss2989190916 Nov 08, 2017 (151)
67 BIOINF_KMB_FNS_UNIBA ss3023995188 Nov 08, 2017 (151)
68 CSHL ss3344135254 Nov 08, 2017 (151)
69 ILLUMINA ss3628021538 Oct 11, 2018 (152)
70 ILLUMINA ss3631557402 Oct 11, 2018 (152)
71 ILLUMINA ss3633193327 Oct 11, 2018 (152)
72 ILLUMINA ss3633904688 Oct 11, 2018 (152)
73 ILLUMINA ss3634757649 Oct 11, 2018 (152)
74 ILLUMINA ss3635591125 Oct 11, 2018 (152)
75 ILLUMINA ss3636443313 Oct 11, 2018 (152)
76 ILLUMINA ss3637342955 Oct 11, 2018 (152)
77 ILLUMINA ss3638249586 Oct 11, 2018 (152)
78 ILLUMINA ss3639129442 Oct 11, 2018 (152)
79 ILLUMINA ss3639869830 Oct 11, 2018 (152)
80 ILLUMINA ss3640464952 Oct 11, 2018 (152)
81 ILLUMINA ss3643220508 Oct 11, 2018 (152)
82 ILLUMINA ss3643918479 Oct 11, 2018 (152)
83 URBANLAB ss3646993596 Oct 11, 2018 (152)
84 EGCUT_WGS ss3657145946 Jul 13, 2019 (153)
85 EVA_DECODE ss3703511575 Jul 13, 2019 (153)
86 ACPOP ss3728266140 Jul 13, 2019 (153)
87 ILLUMINA ss3745057594 Jul 13, 2019 (153)
88 EVA ss3756517246 Jul 13, 2019 (153)
89 ILLUMINA ss3772554461 Jul 13, 2019 (153)
90 PACBIO ss3783814091 Jul 13, 2019 (153)
91 PACBIO ss3789409430 Jul 13, 2019 (153)
92 PACBIO ss3794282208 Jul 13, 2019 (153)
93 KHV_HUMAN_GENOMES ss3800896519 Jul 13, 2019 (153)
94 EVA ss3826886290 Apr 25, 2020 (154)
95 EVA ss3836850440 Apr 25, 2020 (154)
96 EVA ss3842265107 Apr 25, 2020 (154)
97 HGDP ss3847610931 Apr 25, 2020 (154)
98 SGDP_PRJ ss3851865732 Apr 25, 2020 (154)
99 KRGDB ss3897283431 Apr 25, 2020 (154)
100 KOGIC ss3947378011 Apr 25, 2020 (154)
101 EVA ss3984881367 Apr 26, 2021 (155)
102 TOPMED ss4498771993 Apr 26, 2021 (155)
103 TOMMO_GENOMICS ss5150471219 Apr 26, 2021 (155)
104 1000G_HIGH_COVERAGE ss5247377844 Oct 17, 2022 (156)
105 EVA ss5314720031 Oct 17, 2022 (156)
106 EVA ss5327666309 Oct 17, 2022 (156)
107 HUGCELL_USP ss5447643892 Oct 17, 2022 (156)
108 1000G_HIGH_COVERAGE ss5522236379 Oct 17, 2022 (156)
109 SANFORD_IMAGENETICS ss5628354375 Oct 17, 2022 (156)
110 TOMMO_GENOMICS ss5678839121 Oct 17, 2022 (156)
111 YY_MCH ss5802037640 Oct 17, 2022 (156)
112 EVA ss5819834143 Oct 17, 2022 (156)
113 EVA ss5929565021 Oct 17, 2022 (156)
114 EVA ss5954558158 Oct 17, 2022 (156)
115 1000Genomes NC_000002.11 - 29318077 Oct 11, 2018 (152)
116 1000Genomes_30x NC_000002.12 - 29095211 Oct 17, 2022 (156)
117 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 29318077 Oct 11, 2018 (152)
118 Genome-wide autozygosity in Daghestan NC_000002.10 - 29171581 Apr 25, 2020 (154)
119 Genetic variation in the Estonian population NC_000002.11 - 29318077 Oct 11, 2018 (152)
120 The Danish reference pan genome NC_000002.11 - 29318077 Apr 25, 2020 (154)
121 gnomAD - Genomes NC_000002.12 - 29095211 Apr 26, 2021 (155)
122 Genome of the Netherlands Release 5 NC_000002.11 - 29318077 Apr 25, 2020 (154)
123 HGDP-CEPH-db Supplement 1 NC_000002.10 - 29171581 Apr 25, 2020 (154)
124 HapMap NC_000002.12 - 29095211 Apr 25, 2020 (154)
125 KOREAN population from KRGDB NC_000002.11 - 29318077 Apr 25, 2020 (154)
126 Korean Genome Project NC_000002.12 - 29095211 Apr 25, 2020 (154)
127 Medical Genome Project healthy controls from Spanish population NC_000002.11 - 29318077 Apr 25, 2020 (154)
128 Northern Sweden NC_000002.11 - 29318077 Jul 13, 2019 (153)
129 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000002.11 - 29318077 Apr 26, 2021 (155)
130 Qatari NC_000002.11 - 29318077 Apr 25, 2020 (154)
131 SGDP_PRJ NC_000002.11 - 29318077 Apr 25, 2020 (154)
132 Siberian NC_000002.11 - 29318077 Apr 25, 2020 (154)
133 8.3KJPN NC_000002.11 - 29318077 Apr 26, 2021 (155)
134 14KJPN NC_000002.12 - 29095211 Oct 17, 2022 (156)
135 TopMed NC_000002.12 - 29095211 Apr 26, 2021 (155)
136 UK 10K study - Twins NC_000002.11 - 29318077 Oct 11, 2018 (152)
137 ALFA NC_000002.12 - 29095211 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)
rs60475673 May 26, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss84677094, ss3639129442, ss3639869830, ss3643918479 NC_000002.9:29229727:A:G NC_000002.12:29095210:A:G (self)
236292, 288823, ss91100164, ss109359179, ss110000735, ss117636427, ss163231529, ss200205807, ss276398312, ss284314559, ss292534034, ss479811559, ss1397286118, ss1586031492, ss1712440948, ss2635087462, ss3643220508, ss3847610931 NC_000002.10:29171580:A:G NC_000002.12:29095210:A:G (self)
7360974, 4086488, 2884194, 4970662, 1794738, 4460825, 75125, 1551005, 107294, 1899958, 3882712, 1018555, 8440526, 4086488, ss219139481, ss231090292, ss238662840, ss479818670, ss480403156, ss484704278, ss536810448, ss555439564, ss649019950, ss778789318, ss782798906, ss783764468, ss832051850, ss832744985, ss834249348, ss976625811, ss1068960502, ss1296440931, ss1428517556, ss1578794758, ss1603091996, ss1646086029, ss1710958373, ss1752351442, ss1796469809, ss1919858028, ss1968724126, ss2020457500, ss2148502201, ss2633588967, ss2703063240, ss2771230299, ss2989190916, ss3344135254, ss3628021538, ss3631557402, ss3633193327, ss3633904688, ss3634757649, ss3635591125, ss3636443313, ss3637342955, ss3638249586, ss3640464952, ss3657145946, ss3728266140, ss3745057594, ss3756517246, ss3772554461, ss3783814091, ss3789409430, ss3794282208, ss3826886290, ss3836850440, ss3851865732, ss3897283431, ss3984881367, ss5150471219, ss5314720031, ss5327666309, ss5628354375, ss5819834143, ss5954558158 NC_000002.11:29318076:A:G NC_000002.12:29095210:A:G (self)
9762314, 52310593, 1760459, 3756012, 12676225, 302594872, 3405287294, ss2228623584, ss3023995188, ss3646993596, ss3703511575, ss3800896519, ss3842265107, ss3947378011, ss4498771993, ss5247377844, ss5447643892, ss5522236379, ss5678839121, ss5802037640, ss5929565021 NC_000002.12:29095210:A:G NC_000002.12:29095210:A:G (self)
ss21635612, ss23093828 NT_022184.13:8134009:A:G NC_000002.12:29095210:A:G (self)
ss41587378, ss67035704, ss67359519, ss68137768, ss68807827, ss70582927, ss71125443, ss75568241, ss85267046, ss135907155, ss153274163, ss156844000, ss159232647, ss160296589, ss172231091 NT_022184.15:8139963:A:G NC_000002.12:29095210:A:G (self)
4460825, ss3897283431 NC_000002.11:29318076:A:T NC_000002.12:29095210:A:T (self)
3405287294 NC_000002.12:29095210:A:T NC_000002.12:29095210: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 rs12714263

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