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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.

rs1292081

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:27644991 (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>C / A>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.145851 (45998/315376, ALFA)
G=0.260811 (69034/264690, TOPMED)
G=0.247025 (34626/140172, GnomAD) (+ 20 more)
G=0.27914 (7888/28258, 14KJPN)
G=0.27858 (4669/16760, 8.3KJPN)
G=0.3268 (2093/6404, 1000G_30x)
G=0.3275 (1640/5008, 1000G)
G=0.0705 (316/4480, Estonian)
G=0.1290 (497/3854, ALSPAC)
G=0.1327 (492/3708, TWINSUK)
G=0.2918 (855/2930, KOREAN)
G=0.2022 (421/2082, HGDP_Stanford)
G=0.3872 (731/1888, HapMap)
G=0.2986 (547/1832, Korea1K)
G=0.122 (122/998, GoNL)
G=0.275 (212/772, PRJEB37584)
G=0.110 (69/626, Chileans)
G=0.073 (44/600, NorthernSweden)
G=0.259 (56/216, Qatari)
G=0.364 (78/214, Vietnamese)
A=0.342 (63/184, SGDP_PRJ)
G=0.24 (20/82, Ancient Sardinia)
G=0.05 (2/40, 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 315470 A=0.854129 G=0.145871
European Sub 277220 A=0.870507 G=0.129493
African Sub 8622 A=0.4770 G=0.5230
African Others Sub 330 A=0.418 G=0.582
African American Sub 8292 A=0.4794 G=0.5206
Asian Sub 3960 A=0.6775 G=0.3225
East Asian Sub 3184 A=0.6796 G=0.3204
Other Asian Sub 776 A=0.669 G=0.331
Latin American 1 Sub 1278 A=0.7191 G=0.2809
Latin American 2 Sub 9380 A=0.8953 G=0.1047
South Asian Sub 5234 A=0.7784 G=0.2216
Other Sub 9776 A=0.8125 G=0.1875


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 315376 A=0.854149 G=0.145851
Allele Frequency Aggregator European Sub 277144 A=0.870537 G=0.129463
Allele Frequency Aggregator Other Sub 9758 A=0.8124 G=0.1876
Allele Frequency Aggregator Latin American 2 Sub 9380 A=0.8953 G=0.1047
Allele Frequency Aggregator African Sub 8622 A=0.4770 G=0.5230
Allele Frequency Aggregator South Asian Sub 5234 A=0.7784 G=0.2216
Allele Frequency Aggregator Asian Sub 3960 A=0.6775 G=0.3225
Allele Frequency Aggregator Latin American 1 Sub 1278 A=0.7191 G=0.2809
TopMed Global Study-wide 264690 A=0.739189 G=0.260811
gnomAD - Genomes Global Study-wide 140172 A=0.752975 G=0.247025
gnomAD - Genomes European Sub 75940 A=0.87955 G=0.12045
gnomAD - Genomes African Sub 41984 A=0.49016 G=0.50984
gnomAD - Genomes American Sub 13650 A=0.85421 G=0.14579
gnomAD - Genomes Ashkenazi Jewish Sub 3322 A=0.8691 G=0.1309
gnomAD - Genomes East Asian Sub 3122 A=0.6400 G=0.3600
gnomAD - Genomes Other Sub 2154 A=0.7563 G=0.2437
14KJPN JAPANESE Study-wide 28258 A=0.72086 G=0.27914
8.3KJPN JAPANESE Study-wide 16760 A=0.72142 G=0.27858
1000Genomes_30x Global Study-wide 6404 A=0.6732 G=0.3268
1000Genomes_30x African Sub 1786 A=0.4233 G=0.5767
1000Genomes_30x Europe Sub 1266 A=0.8333 G=0.1667
1000Genomes_30x South Asian Sub 1202 A=0.7304 G=0.2696
1000Genomes_30x East Asian Sub 1170 A=0.6342 G=0.3658
1000Genomes_30x American Sub 980 A=0.898 G=0.102
1000Genomes Global Study-wide 5008 A=0.6725 G=0.3275
1000Genomes African Sub 1322 A=0.4070 G=0.5930
1000Genomes East Asian Sub 1008 A=0.6399 G=0.3601
1000Genomes Europe Sub 1006 A=0.8400 G=0.1600
1000Genomes South Asian Sub 978 A=0.735 G=0.265
1000Genomes American Sub 694 A=0.895 G=0.105
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.9295 G=0.0705
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.8710 G=0.1290
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.8673 G=0.1327
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.7082 C=0.0000, G=0.2918
HGDP-CEPH-db Supplement 1 Global Study-wide 2082 A=0.7978 G=0.2022
HGDP-CEPH-db Supplement 1 Est_Asia Sub 470 A=0.766 G=0.234
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.833 G=0.167
HGDP-CEPH-db Supplement 1 Middle_Est Sub 350 A=0.789 G=0.211
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.863 G=0.138
HGDP-CEPH-db Supplement 1 Africa Sub 240 A=0.500 G=0.500
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.986 G=0.014
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.99 G=0.01
HapMap Global Study-wide 1888 A=0.6128 G=0.3872
HapMap American Sub 770 A=0.753 G=0.247
HapMap African Sub 688 A=0.376 G=0.624
HapMap Asian Sub 254 A=0.705 G=0.295
HapMap Europe Sub 176 A=0.790 G=0.210
Korean Genome Project KOREAN Study-wide 1832 A=0.7014 G=0.2986
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.878 G=0.122
CNV burdens in cranial meningiomas Global Study-wide 772 A=0.725 G=0.275
CNV burdens in cranial meningiomas CRM Sub 772 A=0.725 G=0.275
Chileans Chilean Study-wide 626 A=0.890 G=0.110
Northern Sweden ACPOP Study-wide 600 A=0.927 G=0.073
Qatari Global Study-wide 216 A=0.741 G=0.259
A Vietnamese Genetic Variation Database Global Study-wide 214 A=0.636 G=0.364
SGDP_PRJ Global Study-wide 184 A=0.342 G=0.658
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 82 A=0.76 G=0.24
The Danish reference pan genome Danish Study-wide 40 A=0.95 G=0.05
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.27644991A>C
GRCh38.p14 chr 1 NC_000001.11:g.27644991A>G
GRCh37.p13 chr 1 NC_000001.10:g.27971502A>C
GRCh37.p13 chr 1 NC_000001.10:g.27971502A>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= C G
GRCh38.p14 chr 1 NC_000001.11:g.27644991= NC_000001.11:g.27644991A>C NC_000001.11:g.27644991A>G
GRCh37.p13 chr 1 NC_000001.10:g.27971502= NC_000001.10:g.27971502A>C NC_000001.10:g.27971502A>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#.

123 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 KWOK ss2045858 Oct 18, 2000 (87)
2 SC_JCM ss2625141 Nov 09, 2000 (123)
3 YUSUKE ss2991872 Jun 15, 2001 (98)
4 PERLEGEN ss16333722 Feb 28, 2004 (123)
5 PERLEGEN ss23147961 Sep 20, 2004 (123)
6 ILLUMINA ss65789349 Oct 14, 2006 (127)
7 AFFY ss65920120 Nov 29, 2006 (127)
8 AFFY ss66106766 Nov 29, 2006 (127)
9 ILLUMINA ss66702493 Nov 29, 2006 (127)
10 ILLUMINA ss67046761 Nov 29, 2006 (127)
11 ILLUMINA ss67372276 Nov 29, 2006 (127)
12 ILLUMINA ss70417411 May 16, 2007 (127)
13 ILLUMINA ss70588637 May 25, 2008 (130)
14 ILLUMINA ss71131948 May 16, 2007 (127)
15 ILLUMINA ss75655520 Dec 06, 2007 (129)
16 AFFY ss76081712 Dec 08, 2007 (129)
17 KRIBB_YJKIM ss83713878 Dec 15, 2007 (130)
18 ILLUMINA-UK ss118581944 Feb 14, 2009 (130)
19 ILLUMINA ss121609833 Dec 01, 2009 (131)
20 ILLUMINA ss153295735 Dec 01, 2009 (131)
21 ILLUMINA ss159238946 Dec 01, 2009 (131)
22 ILLUMINA ss160306974 Dec 01, 2009 (131)
23 COMPLETE_GENOMICS ss166278619 Jul 04, 2010 (132)
24 ILLUMINA ss170255251 Jul 04, 2010 (132)
25 ILLUMINA ss172278029 Jul 04, 2010 (132)
26 AFFY ss172438079 Jul 04, 2010 (132)
27 BUSHMAN ss198210911 Jul 04, 2010 (132)
28 1000GENOMES ss218296067 Jul 14, 2010 (132)
29 1000GENOMES ss230471131 Jul 14, 2010 (132)
30 1000GENOMES ss238176576 Jul 15, 2010 (132)
31 GMI ss275762441 May 04, 2012 (137)
32 GMI ss284023433 Apr 25, 2013 (138)
33 ILLUMINA ss479842068 May 04, 2012 (137)
34 ILLUMINA ss479849544 May 04, 2012 (137)
35 ILLUMINA ss480444588 Sep 08, 2015 (146)
36 ILLUMINA ss484719525 May 04, 2012 (137)
37 ILLUMINA ss536821993 Sep 08, 2015 (146)
38 TISHKOFF ss553920904 Apr 25, 2013 (138)
39 SSMP ss647656536 Apr 25, 2013 (138)
40 ILLUMINA ss779032289 Sep 08, 2015 (146)
41 ILLUMINA ss782806483 Sep 08, 2015 (146)
42 ILLUMINA ss783771852 Sep 08, 2015 (146)
43 ILLUMINA ss825386685 Apr 01, 2015 (144)
44 ILLUMINA ss832059596 Sep 08, 2015 (146)
45 ILLUMINA ss832751268 Jul 12, 2019 (153)
46 ILLUMINA ss834495027 Sep 08, 2015 (146)
47 EVA-GONL ss974974371 Aug 21, 2014 (142)
48 1000GENOMES ss1290150741 Aug 21, 2014 (142)
49 DDI ss1425754699 Apr 01, 2015 (144)
50 EVA_GENOME_DK ss1573956198 Apr 01, 2015 (144)
51 EVA_DECODE ss1584333834 Apr 01, 2015 (144)
52 EVA_UK10K_ALSPAC ss1599785511 Apr 01, 2015 (144)
53 EVA_UK10K_TWINSUK ss1642779544 Apr 01, 2015 (144)
54 EVA_SVP ss1712319872 Apr 01, 2015 (144)
55 ILLUMINA ss1751913890 Sep 08, 2015 (146)
56 HAMMER_LAB ss1794100617 Sep 08, 2015 (146)
57 WEILL_CORNELL_DGM ss1918186308 Feb 12, 2016 (147)
58 ILLUMINA ss1945989339 Feb 12, 2016 (147)
59 ILLUMINA ss1958256228 Feb 12, 2016 (147)
60 AMU ss1971465599 Jul 19, 2016 (147)
61 JJLAB ss2019604623 Sep 14, 2016 (149)
62 HUMAN_LONGEVITY ss2160962760 Dec 20, 2016 (150)
63 SYSTEMSBIOZJU ss2624318904 Nov 08, 2017 (151)
64 ILLUMINA ss2632493430 Nov 08, 2017 (151)
65 ILLUMINA ss2634997108 Nov 08, 2017 (151)
66 GRF ss2697517623 Nov 08, 2017 (151)
67 ILLUMINA ss2710668466 Nov 08, 2017 (151)
68 GNOMAD ss2753011270 Nov 08, 2017 (151)
69 AFFY ss2984852396 Nov 08, 2017 (151)
70 AFFY ss2985503514 Nov 08, 2017 (151)
71 SWEGEN ss2986514063 Nov 08, 2017 (151)
72 ILLUMINA ss3021069908 Nov 08, 2017 (151)
73 BIOINF_KMB_FNS_UNIBA ss3023567701 Nov 08, 2017 (151)
74 CSHL ss3343378520 Nov 08, 2017 (151)
75 ILLUMINA ss3625529019 Oct 11, 2018 (152)
76 ILLUMINA ss3626055357 Oct 11, 2018 (152)
77 ILLUMINA ss3630530742 Oct 11, 2018 (152)
78 ILLUMINA ss3632885241 Oct 11, 2018 (152)
79 ILLUMINA ss3633579413 Oct 11, 2018 (152)
80 ILLUMINA ss3634314490 Oct 11, 2018 (152)
81 ILLUMINA ss3635273422 Oct 11, 2018 (152)
82 ILLUMINA ss3635990353 Oct 11, 2018 (152)
83 ILLUMINA ss3637023807 Oct 11, 2018 (152)
84 ILLUMINA ss3637745015 Oct 11, 2018 (152)
85 ILLUMINA ss3638893044 Oct 11, 2018 (152)
86 ILLUMINA ss3639443660 Oct 11, 2018 (152)
87 ILLUMINA ss3640021852 Oct 11, 2018 (152)
88 ILLUMINA ss3642758204 Oct 11, 2018 (152)
89 ILLUMINA ss3644485214 Oct 11, 2018 (152)
90 ILLUMINA ss3651395380 Oct 11, 2018 (152)
91 ILLUMINA ss3653624845 Oct 11, 2018 (152)
92 EGCUT_WGS ss3654578189 Jul 12, 2019 (153)
93 EVA_DECODE ss3686405342 Jul 12, 2019 (153)
94 ACPOP ss3726892065 Jul 12, 2019 (153)
95 ILLUMINA ss3744043712 Jul 12, 2019 (153)
96 ILLUMINA ss3744615440 Jul 12, 2019 (153)
97 EVA ss3745974731 Jul 12, 2019 (153)
98 ILLUMINA ss3772116981 Jul 12, 2019 (153)
99 KHV_HUMAN_GENOMES ss3798994117 Jul 12, 2019 (153)
100 EVA ss3826085051 Apr 25, 2020 (154)
101 HGDP ss3847328099 Apr 25, 2020 (154)
102 SGDP_PRJ ss3848469762 Apr 25, 2020 (154)
103 KRGDB ss3893399334 Apr 25, 2020 (154)
104 KOGIC ss3944104643 Apr 25, 2020 (154)
105 EVA ss3984454288 Apr 27, 2021 (155)
106 EVA ss3984785619 Apr 27, 2021 (155)
107 EVA ss4016899929 Apr 27, 2021 (155)
108 TOPMED ss4443161375 Apr 27, 2021 (155)
109 TOMMO_GENOMICS ss5143074034 Apr 27, 2021 (155)
110 1000G_HIGH_COVERAGE ss5241614327 Oct 17, 2022 (156)
111 EVA ss5314602614 Oct 17, 2022 (156)
112 EVA ss5317526621 Oct 17, 2022 (156)
113 HUGCELL_USP ss5442751719 Oct 17, 2022 (156)
114 EVA ss5505796340 Oct 17, 2022 (156)
115 1000G_HIGH_COVERAGE ss5513572096 Oct 17, 2022 (156)
116 SANFORD_IMAGENETICS ss5625168233 Oct 17, 2022 (156)
117 TOMMO_GENOMICS ss5667563085 Oct 17, 2022 (156)
118 EVA ss5799478847 Oct 17, 2022 (156)
119 YY_MCH ss5800436677 Oct 17, 2022 (156)
120 EVA ss5831708984 Oct 17, 2022 (156)
121 EVA ss5848833066 Oct 17, 2022 (156)
122 EVA ss5907512748 Oct 17, 2022 (156)
123 EVA ss5936984758 Oct 17, 2022 (156)
124 1000Genomes NC_000001.10 - 27971502 Oct 11, 2018 (152)
125 1000Genomes_30x NC_000001.11 - 27644991 Oct 17, 2022 (156)
126 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 27971502 Oct 11, 2018 (152)
127 Chileans NC_000001.10 - 27971502 Apr 25, 2020 (154)
128 Genetic variation in the Estonian population NC_000001.10 - 27971502 Oct 11, 2018 (152)
129 The Danish reference pan genome NC_000001.10 - 27971502 Apr 25, 2020 (154)
130 gnomAD - Genomes NC_000001.11 - 27644991 Apr 27, 2021 (155)
131 Genome of the Netherlands Release 5 NC_000001.10 - 27971502 Apr 25, 2020 (154)
132 HGDP-CEPH-db Supplement 1 NC_000001.9 - 27844089 Apr 25, 2020 (154)
133 HapMap NC_000001.11 - 27644991 Apr 25, 2020 (154)
134 KOREAN population from KRGDB NC_000001.10 - 27971502 Apr 25, 2020 (154)
135 Korean Genome Project NC_000001.11 - 27644991 Apr 25, 2020 (154)
136 Northern Sweden NC_000001.10 - 27971502 Jul 12, 2019 (153)
137 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 27971502 Apr 27, 2021 (155)
138 CNV burdens in cranial meningiomas NC_000001.10 - 27971502 Apr 27, 2021 (155)
139 Qatari NC_000001.10 - 27971502 Apr 25, 2020 (154)
140 SGDP_PRJ NC_000001.10 - 27971502 Apr 25, 2020 (154)
141 8.3KJPN NC_000001.10 - 27971502 Apr 27, 2021 (155)
142 14KJPN NC_000001.11 - 27644991 Oct 17, 2022 (156)
143 TopMed NC_000001.11 - 27644991 Apr 27, 2021 (155)
144 UK 10K study - Twins NC_000001.10 - 27971502 Oct 11, 2018 (152)
145 A Vietnamese Genetic Variation Database NC_000001.10 - 27971502 Jul 12, 2019 (153)
146 ALFA NC_000001.11 - 27644991 Apr 27, 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)
rs1767515 Sep 24, 2004 (123)
rs2076461 Aug 15, 2001 (98)
rs11564795 Sep 24, 2004 (123)
rs17162691 Oct 07, 2004 (123)
rs59643206 May 25, 2008 (130)
rs386526570 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
576728, ss3893399334 NC_000001.10:27971501:A:C NC_000001.11:27644990:A:C (self)
ss3638893044, ss3639443660 NC_000001.8:27655643:A:G NC_000001.11:27644990:A:G (self)
5991, ss118581944, ss160306974, ss166278619, ss198210911, ss275762441, ss284023433, ss479842068, ss825386685, ss1584333834, ss1712319872, ss2634997108, ss3642758204, ss3847328099 NC_000001.9:27844088:A:G NC_000001.11:27644990:A:G (self)
842937, 448907, 4286, 316437, 1435431, 192861, 576728, 176930, 11546, 3590, 228238, 486742, 1043341, 448907, 93348, ss218296067, ss230471131, ss238176576, ss479849544, ss480444588, ss484719525, ss536821993, ss553920904, ss647656536, ss779032289, ss782806483, ss783771852, ss832059596, ss832751268, ss834495027, ss974974371, ss1290150741, ss1425754699, ss1573956198, ss1599785511, ss1642779544, ss1751913890, ss1794100617, ss1918186308, ss1945989339, ss1958256228, ss1971465599, ss2019604623, ss2624318904, ss2632493430, ss2697517623, ss2710668466, ss2753011270, ss2984852396, ss2985503514, ss2986514063, ss3021069908, ss3343378520, ss3625529019, ss3626055357, ss3630530742, ss3632885241, ss3633579413, ss3634314490, ss3635273422, ss3635990353, ss3637023807, ss3637745015, ss3640021852, ss3644485214, ss3651395380, ss3653624845, ss3654578189, ss3726892065, ss3744043712, ss3744615440, ss3745974731, ss3772116981, ss3826085051, ss3848469762, ss3893399334, ss3984454288, ss3984785619, ss4016899929, ss5143074034, ss5314602614, ss5317526621, ss5505796340, ss5625168233, ss5799478847, ss5831708984, ss5936984758 NC_000001.10:27971501:A:G NC_000001.11:27644990:A:G (self)
1098031, 5928539, 34626, 482644, 1400189, 6767710, 13795798389, ss2160962760, ss3023567701, ss3686405342, ss3798994117, ss3944104643, ss4443161375, ss5241614327, ss5442751719, ss5513572096, ss5667563085, ss5800436677, ss5848833066, ss5907512748 NC_000001.11:27644990:A:G NC_000001.11:27644990:A:G (self)
ss2045858, ss2625141, ss2991872, ss16333722, ss23147961, ss65789349, ss65920120, ss66106766, ss66702493, ss67046761, ss67372276, ss70417411, ss70588637, ss71131948, ss75655520, ss76081712, ss83713878, ss121609833, ss153295735, ss159238946, ss170255251, ss172278029, ss172438079 NT_004610.19:14651589:A:G NC_000001.11:27644990: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 rs1292081

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