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.

rs921120

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr2:45045902 (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 / A>T
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.220628 (58398/264690, TOPMED)
A=0.296552 (57769/194802, ALFA)
A=0.05708 (1613/28258, 14KJPN) (+ 18 more)
A=0.05823 (976/16760, 8.3KJPN)
A=0.1524 (976/6404, 1000G_30x)
A=0.1508 (755/5008, 1000G)
A=0.2915 (1306/4480, Estonian)
A=0.3031 (1168/3854, ALSPAC)
A=0.3344 (1240/3708, TWINSUK)
A=0.0604 (177/2930, KOREAN)
A=0.1587 (330/2080, HGDP_Stanford)
A=0.1210 (229/1892, HapMap)
A=0.0573 (105/1832, Korea1K)
A=0.330 (329/998, GoNL)
A=0.333 (200/600, NorthernSweden)
A=0.114 (62/544, SGDP_PRJ)
A=0.199 (43/216, Qatari)
A=0.124 (26/210, Vietnamese)
G=0.44 (30/68, Ancient Sardinia)
A=0.14 (8/56, Siberian)
A=0.35 (14/40, 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: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 194802 A=0.296552 G=0.703448, T=0.000000 0.094496 0.501391 0.404113 32
European Sub 167566 A=0.315249 G=0.684751, T=0.000000 0.103386 0.472888 0.423726 16
African Sub 5510 A=0.1147 G=0.8853, T=0.0000 0.018149 0.788748 0.193103 4
African Others Sub 194 A=0.062 G=0.938, T=0.000 0.010309 0.886598 0.103093 1
African American Sub 5316 A=0.1166 G=0.8834, T=0.0000 0.018435 0.785177 0.196388 4
Asian Sub 642 A=0.104 G=0.896, T=0.000 0.012461 0.803738 0.183801 0
East Asian Sub 488 A=0.082 G=0.918, T=0.000 0.008197 0.844262 0.147541 0
Other Asian Sub 154 A=0.175 G=0.825, T=0.000 0.025974 0.675325 0.298701 0
Latin American 1 Sub 850 A=0.254 G=0.746, T=0.000 0.072941 0.564706 0.362353 1
Latin American 2 Sub 8468 A=0.1621 G=0.8379, T=0.0000 0.029523 0.705243 0.265234 2
South Asian Sub 4946 A=0.1557 G=0.8443, T=0.0000 0.027901 0.716539 0.25556 1
Other Sub 6820 A=0.2765 G=0.7235, T=0.0000 0.077126 0.524047 0.398827 0


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=0.220628 G=0.779372
Allele Frequency Aggregator Total Global 194802 A=0.296552 G=0.703448, T=0.000000
Allele Frequency Aggregator European Sub 167566 A=0.315249 G=0.684751, T=0.000000
Allele Frequency Aggregator Latin American 2 Sub 8468 A=0.1621 G=0.8379, T=0.0000
Allele Frequency Aggregator Other Sub 6820 A=0.2765 G=0.7235, T=0.0000
Allele Frequency Aggregator African Sub 5510 A=0.1147 G=0.8853, T=0.0000
Allele Frequency Aggregator South Asian Sub 4946 A=0.1557 G=0.8443, T=0.0000
Allele Frequency Aggregator Latin American 1 Sub 850 A=0.254 G=0.746, T=0.000
Allele Frequency Aggregator Asian Sub 642 A=0.104 G=0.896, T=0.000
14KJPN JAPANESE Study-wide 28258 A=0.05708 G=0.94292
8.3KJPN JAPANESE Study-wide 16760 A=0.05823 G=0.94177
1000Genomes_30x Global Study-wide 6404 A=0.1524 G=0.8476
1000Genomes_30x African Sub 1786 A=0.0700 G=0.9300
1000Genomes_30x Europe Sub 1266 A=0.3104 G=0.6896
1000Genomes_30x South Asian Sub 1202 A=0.1331 G=0.8669
1000Genomes_30x East Asian Sub 1170 A=0.1103 G=0.8897
1000Genomes_30x American Sub 980 A=0.172 G=0.828
1000Genomes Global Study-wide 5008 A=0.1508 G=0.8492
1000Genomes African Sub 1322 A=0.0635 G=0.9365
1000Genomes East Asian Sub 1008 A=0.1042 G=0.8958
1000Genomes Europe Sub 1006 A=0.3022 G=0.6978
1000Genomes South Asian Sub 978 A=0.134 G=0.866
1000Genomes American Sub 694 A=0.189 G=0.811
Genetic variation in the Estonian population Estonian Study-wide 4480 A=0.2915 G=0.7085
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 A=0.3031 G=0.6969
UK 10K study - Twins TWIN COHORT Study-wide 3708 A=0.3344 G=0.6656
KOREAN population from KRGDB KOREAN Study-wide 2930 A=0.0604 C=0.0000, G=0.9396, T=0.0000
HGDP-CEPH-db Supplement 1 Global Study-wide 2080 A=0.1587 G=0.8413
HGDP-CEPH-db Supplement 1 Est_Asia Sub 468 A=0.085 G=0.915
HGDP-CEPH-db Supplement 1 Central_South_Asia Sub 414 A=0.157 G=0.843
HGDP-CEPH-db Supplement 1 Middle_Est Sub 348 A=0.250 G=0.750
HGDP-CEPH-db Supplement 1 Europe Sub 320 A=0.309 G=0.691
HGDP-CEPH-db Supplement 1 Africa Sub 242 A=0.074 G=0.926
HGDP-CEPH-db Supplement 1 America Sub 216 A=0.000 G=1.000
HGDP-CEPH-db Supplement 1 Oceania Sub 72 A=0.29 G=0.71
HapMap Global Study-wide 1892 A=0.1210 G=0.8790
HapMap American Sub 770 A=0.170 G=0.830
HapMap African Sub 692 A=0.055 G=0.945
HapMap Asian Sub 254 A=0.055 G=0.945
HapMap Europe Sub 176 A=0.261 G=0.739
Korean Genome Project KOREAN Study-wide 1832 A=0.0573 G=0.9427
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 A=0.330 G=0.670
Northern Sweden ACPOP Study-wide 600 A=0.333 G=0.667
SGDP_PRJ Global Study-wide 544 A=0.114 G=0.886
Qatari Global Study-wide 216 A=0.199 G=0.801
A Vietnamese Genetic Variation Database Global Study-wide 210 A=0.124 G=0.876
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 68 A=0.56 G=0.44
Siberian Global Study-wide 56 A=0.14 G=0.86
The Danish reference pan genome Danish Study-wide 40 A=0.35 G=0.65
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.45045902A>C
GRCh38.p14 chr 2 NC_000002.12:g.45045902A>G
GRCh38.p14 chr 2 NC_000002.12:g.45045902A>T
GRCh37.p13 chr 2 NC_000002.11:g.45273041A>C
GRCh37.p13 chr 2 NC_000002.11:g.45273041A>G
GRCh37.p13 chr 2 NC_000002.11:g.45273041A>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= C G T
GRCh38.p14 chr 2 NC_000002.12:g.45045902= NC_000002.12:g.45045902A>C NC_000002.12:g.45045902A>G NC_000002.12:g.45045902A>T
GRCh37.p13 chr 2 NC_000002.11:g.45273041= NC_000002.11:g.45273041A>C NC_000002.11:g.45273041A>G NC_000002.11:g.45273041A>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#.

131 SubSNP, 23 Frequency submissions
No Submitter Submission ID Date (Build)
1 TSC-CSHL ss1357632 Oct 05, 2000 (86)
2 WI_SSAHASNP ss11491354 Jul 11, 2003 (116)
3 CSHL-HAPMAP ss17676232 Feb 27, 2004 (120)
4 SSAHASNP ss21683246 Apr 05, 2004 (121)
5 ABI ss41569882 Mar 14, 2006 (126)
6 AFFY ss66143388 Dec 01, 2006 (127)
7 ILLUMINA ss66790106 Dec 01, 2006 (127)
8 ILLUMINA ss67895410 Dec 01, 2006 (127)
9 ILLUMINA ss68030049 Dec 01, 2006 (127)
10 PERLEGEN ss68812049 May 17, 2007 (127)
11 ILLUMINA ss71594700 May 17, 2007 (127)
12 ILLUMINA ss75789826 Dec 07, 2007 (129)
13 AFFY ss76163840 Dec 07, 2007 (129)
14 ILLUMINA ss79289633 Dec 15, 2007 (130)
15 KRIBB_YJKIM ss83612454 Dec 15, 2007 (130)
16 HGSV ss85136116 Dec 15, 2007 (130)
17 HGSV ss85315545 Dec 15, 2007 (130)
18 BCMHGSC_JDW ss91144627 Mar 24, 2008 (129)
19 HUMANGENOME_JCVI ss96393302 Feb 05, 2009 (130)
20 ILLUMINA ss98236870 May 24, 2008 (130)
21 BGI ss106085595 Feb 05, 2009 (130)
22 1000GENOMES ss109466654 Jan 24, 2009 (130)
23 1000GENOMES ss110188635 Jan 24, 2009 (130)
24 ILLUMINA-UK ss117686340 Dec 01, 2009 (131)
25 ILLUMINA ss122951582 Dec 01, 2009 (131)
26 ENSEMBL ss135867008 Dec 01, 2009 (131)
27 ENSEMBL ss138435316 Dec 01, 2009 (131)
28 ILLUMINA ss154481723 Dec 01, 2009 (131)
29 GMI ss157000988 Dec 01, 2009 (131)
30 ILLUMINA ss159656128 Dec 01, 2009 (131)
31 ILLUMINA ss160968201 Dec 01, 2009 (131)
32 COMPLETE_GENOMICS ss163385854 Jul 04, 2010 (132)
33 COMPLETE_GENOMICS ss164293425 Jul 04, 2010 (132)
34 ILLUMINA ss172433028 Jul 04, 2010 (132)
35 AFFY ss172683667 Jul 04, 2010 (132)
36 ILLUMINA ss174785255 Jul 04, 2010 (132)
37 BUSHMAN ss200373095 Jul 04, 2010 (132)
38 BCM-HGSC-SUB ss205737237 Jul 04, 2010 (132)
39 1000GENOMES ss219214633 Jul 14, 2010 (132)
40 1000GENOMES ss231144454 Jul 14, 2010 (132)
41 1000GENOMES ss238704508 Jul 15, 2010 (132)
42 BL ss253076820 May 09, 2011 (134)
43 GMI ss276447919 May 04, 2012 (137)
44 GMI ss284336689 Apr 25, 2013 (138)
45 PJP ss292258883 May 09, 2011 (134)
46 ILLUMINA ss481843724 May 04, 2012 (137)
47 ILLUMINA ss481876390 May 04, 2012 (137)
48 ILLUMINA ss482833340 Sep 08, 2015 (146)
49 ILLUMINA ss485716306 May 04, 2012 (137)
50 ILLUMINA ss537577077 Sep 08, 2015 (146)
51 TISHKOFF ss555525849 Apr 25, 2013 (138)
52 SSMP ss649110145 Apr 25, 2013 (138)
53 ILLUMINA ss779004125 Sep 08, 2015 (146)
54 ILLUMINA ss783303800 Sep 08, 2015 (146)
55 ILLUMINA ss784255997 Sep 08, 2015 (146)
56 ILLUMINA ss825620151 Apr 01, 2015 (144)
57 ILLUMINA ss832565173 Sep 08, 2015 (146)
58 ILLUMINA ss833166922 Jul 13, 2019 (153)
59 ILLUMINA ss834466526 Sep 08, 2015 (146)
60 EVA-GONL ss976764622 Aug 21, 2014 (142)
61 JMKIDD_LAB ss1069065915 Aug 21, 2014 (142)
62 1000GENOMES ss1296971169 Aug 21, 2014 (142)
63 DDI ss1428559984 Apr 01, 2015 (144)
64 EVA_GENOME_DK ss1578852497 Apr 01, 2015 (144)
65 EVA_DECODE ss1586173637 Apr 01, 2015 (144)
66 EVA_UK10K_ALSPAC ss1603373031 Apr 01, 2015 (144)
67 EVA_UK10K_TWINSUK ss1646367064 Apr 01, 2015 (144)
68 EVA_SVP ss1712451028 Apr 01, 2015 (144)
69 ILLUMINA ss1752358020 Sep 08, 2015 (146)
70 HAMMER_LAB ss1796675981 Sep 08, 2015 (146)
71 WEILL_CORNELL_DGM ss1919999723 Feb 12, 2016 (147)
72 GENOMED ss1968756248 Jul 19, 2016 (147)
73 JJLAB ss2020532700 Sep 14, 2016 (149)
74 USC_VALOUEV ss2148576911 Dec 20, 2016 (150)
75 HUMAN_LONGEVITY ss2229724023 Dec 20, 2016 (150)
76 SYSTEMSBIOZJU ss2624778832 Nov 08, 2017 (151)
77 ILLUMINA ss2633606003 Nov 08, 2017 (151)
78 GRF ss2703142449 Nov 08, 2017 (151)
79 GNOMAD ss2772719603 Nov 08, 2017 (151)
80 SWEGEN ss2989402792 Nov 08, 2017 (151)
81 BIOINF_KMB_FNS_UNIBA ss3024032043 Nov 08, 2017 (151)
82 CSHL ss3344199390 Nov 08, 2017 (151)
83 ILLUMINA ss3628050285 Oct 11, 2018 (152)
84 ILLUMINA ss3631573560 Oct 11, 2018 (152)
85 ILLUMINA ss3633197926 Oct 11, 2018 (152)
86 ILLUMINA ss3633909500 Oct 11, 2018 (152)
87 ILLUMINA ss3634763590 Oct 11, 2018 (152)
88 ILLUMINA ss3635595825 Oct 11, 2018 (152)
89 ILLUMINA ss3636449533 Oct 11, 2018 (152)
90 ILLUMINA ss3637347671 Oct 11, 2018 (152)
91 ILLUMINA ss3638256702 Oct 11, 2018 (152)
92 ILLUMINA ss3639133189 Oct 11, 2018 (152)
93 ILLUMINA ss3639578193 Oct 11, 2018 (152)
94 ILLUMINA ss3640470892 Oct 11, 2018 (152)
95 ILLUMINA ss3643226977 Oct 11, 2018 (152)
96 URBANLAB ss3647022728 Oct 11, 2018 (152)
97 EGCUT_WGS ss3657366241 Jul 13, 2019 (153)
98 EVA_DECODE ss3703765006 Jul 13, 2019 (153)
99 ACPOP ss3728380243 Jul 13, 2019 (153)
100 ILLUMINA ss3745063502 Jul 13, 2019 (153)
101 EVA ss3756679203 Jul 13, 2019 (153)
102 ILLUMINA ss3772560341 Jul 13, 2019 (153)
103 PACBIO ss3783848169 Jul 13, 2019 (153)
104 PACBIO ss3789438376 Jul 13, 2019 (153)
105 PACBIO ss3794311196 Jul 13, 2019 (153)
106 KHV_HUMAN_GENOMES ss3801054489 Jul 13, 2019 (153)
107 EVA ss3826952169 Apr 25, 2020 (154)
108 EVA ss3836884630 Apr 25, 2020 (154)
109 EVA ss3842299813 Apr 25, 2020 (154)
110 HGDP ss3847615461 Apr 25, 2020 (154)
111 SGDP_PRJ ss3852136082 Apr 25, 2020 (154)
112 KRGDB ss3897586324 Apr 25, 2020 (154)
113 KOGIC ss3947628036 Apr 25, 2020 (154)
114 EVA ss3984889329 Apr 26, 2021 (155)
115 EVA ss4016992858 Apr 26, 2021 (155)
116 TOPMED ss4503334611 Apr 26, 2021 (155)
117 TOMMO_GENOMICS ss5151062303 Apr 26, 2021 (155)
118 1000G_HIGH_COVERAGE ss5247832933 Oct 12, 2022 (156)
119 EVA ss5314730231 Oct 12, 2022 (156)
120 EVA ss5328503884 Oct 12, 2022 (156)
121 HUGCELL_USP ss5448056869 Oct 12, 2022 (156)
122 EVA ss5506383541 Oct 12, 2022 (156)
123 1000G_HIGH_COVERAGE ss5522923914 Oct 12, 2022 (156)
124 SANFORD_IMAGENETICS ss5628613587 Oct 12, 2022 (156)
125 TOMMO_GENOMICS ss5679600882 Oct 12, 2022 (156)
126 EVA ss5799529891 Oct 12, 2022 (156)
127 YY_MCH ss5802149717 Oct 12, 2022 (156)
128 EVA ss5820010961 Oct 12, 2022 (156)
129 EVA ss5852497003 Oct 12, 2022 (156)
130 EVA ss5930094796 Oct 12, 2022 (156)
131 EVA ss5954832690 Oct 12, 2022 (156)
132 1000Genomes NC_000002.11 - 45273041 Oct 11, 2018 (152)
133 1000Genomes_30x NC_000002.12 - 45045902 Oct 12, 2022 (156)
134 The Avon Longitudinal Study of Parents and Children NC_000002.11 - 45273041 Oct 11, 2018 (152)
135 Genetic variation in the Estonian population NC_000002.11 - 45273041 Oct 11, 2018 (152)
136 The Danish reference pan genome NC_000002.11 - 45273041 Apr 25, 2020 (154)
137 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 56131876 (NC_000002.12:45045901:A:G 106609/140042)
Row 56131877 (NC_000002.12:45045901:A:T 0/140084)

- Apr 26, 2021 (155)
138 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 56131876 (NC_000002.12:45045901:A:G 106609/140042)
Row 56131877 (NC_000002.12:45045901:A:T 0/140084)

- Apr 26, 2021 (155)
139 Genome of the Netherlands Release 5 NC_000002.11 - 45273041 Apr 25, 2020 (154)
140 HGDP-CEPH-db Supplement 1 NC_000002.10 - 45126545 Apr 25, 2020 (154)
141 HapMap NC_000002.12 - 45045902 Apr 25, 2020 (154)
142 KOREAN population from KRGDB NC_000002.11 - 45273041 Apr 25, 2020 (154)
143 Korean Genome Project NC_000002.12 - 45045902 Apr 25, 2020 (154)
144 Northern Sweden NC_000002.11 - 45273041 Jul 13, 2019 (153)
145 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000002.11 - 45273041 Apr 26, 2021 (155)
146 Qatari NC_000002.11 - 45273041 Apr 25, 2020 (154)
147 SGDP_PRJ NC_000002.11 - 45273041 Apr 25, 2020 (154)
148 Siberian NC_000002.11 - 45273041 Apr 25, 2020 (154)
149 8.3KJPN NC_000002.11 - 45273041 Apr 26, 2021 (155)
150 14KJPN NC_000002.12 - 45045902 Oct 12, 2022 (156)
151 TopMed NC_000002.12 - 45045902 Apr 26, 2021 (155)
152 UK 10K study - Twins NC_000002.11 - 45273041 Oct 11, 2018 (152)
153 A Vietnamese Genetic Variation Database NC_000002.11 - 45273041 Jul 13, 2019 (153)
154 ALFA NC_000002.12 - 45045902 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)
rs58840671 May 24, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
4763718, ss3897586324 NC_000002.11:45273040:A:C NC_000002.12:45045901:A:C (self)
ss85136116, ss85315545, ss3639133189, ss3639578193 NC_000002.9:45184691:A:G NC_000002.12:45045901:A:G (self)
293353, ss91144627, ss109466654, ss110188635, ss117686340, ss163385854, ss164293425, ss200373095, ss205737237, ss253076820, ss276447919, ss284336689, ss292258883, ss481843724, ss825620151, ss1586173637, ss1712451028, ss3643226977, ss3847615461 NC_000002.10:45126544:A:G NC_000002.12:45045901:A:G (self)
7907874, 4392110, 3104489, 5025930, 1930077, 4763718, 1665108, 115256, 2041653, 4153062, 1093265, 9031610, 4392110, 955096, ss219214633, ss231144454, ss238704508, ss481876390, ss482833340, ss485716306, ss537577077, ss555525849, ss649110145, ss779004125, ss783303800, ss784255997, ss832565173, ss833166922, ss834466526, ss976764622, ss1069065915, ss1296971169, ss1428559984, ss1578852497, ss1603373031, ss1646367064, ss1752358020, ss1796675981, ss1919999723, ss1968756248, ss2020532700, ss2148576911, ss2624778832, ss2633606003, ss2703142449, ss2772719603, ss2989402792, ss3344199390, ss3628050285, ss3631573560, ss3633197926, ss3633909500, ss3634763590, ss3635595825, ss3636449533, ss3637347671, ss3638256702, ss3640470892, ss3657366241, ss3728380243, ss3745063502, ss3756679203, ss3772560341, ss3783848169, ss3789438376, ss3794311196, ss3826952169, ss3836884630, ss3852136082, ss3897586324, ss3984889329, ss4016992858, ss5151062303, ss5314730231, ss5328503884, ss5506383541, ss5628613587, ss5799529891, ss5820010961, ss5954832690 NC_000002.11:45273040:A:G NC_000002.12:45045901:A:G (self)
10449849, 1785707, 4006037, 13437986, 307157490, 12641411605, ss2229724023, ss3024032043, ss3647022728, ss3703765006, ss3801054489, ss3842299813, ss3947628036, ss4503334611, ss5247832933, ss5448056869, ss5522923914, ss5679600882, ss5802149717, ss5852497003, ss5930094796 NC_000002.12:45045901:A:G NC_000002.12:45045901:A:G (self)
ss11491354 NT_022184.12:24088972:A:G NC_000002.12:45045901:A:G (self)
ss17676232, ss21683246 NT_022184.13:24088972:A:G NC_000002.12:45045901:A:G (self)
ss1357632, ss41569882, ss66143388, ss66790106, ss67895410, ss68030049, ss68812049, ss71594700, ss75789826, ss76163840, ss79289633, ss83612454, ss96393302, ss98236870, ss106085595, ss122951582, ss135867008, ss138435316, ss154481723, ss157000988, ss159656128, ss160968201, ss172433028, ss172683667, ss174785255 NT_022184.15:24094927:A:G NC_000002.12:45045901:A:G (self)
4763718, ss3897586324 NC_000002.11:45273040:A:T NC_000002.12:45045901:A:T (self)
12641411605, ss2229724023 NC_000002.12:45045901:A:T NC_000002.12:45045901: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 rs921120

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.post820+afb47a3d