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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.

rs2481

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr22:36281354 (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
G>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.158030 (41829/264690, TOPMED)
A=0.149740 (38043/254060, ALFA)
A=0.151035 (21169/140160, GnomAD) (+ 19 more)
A=0.22622 (17789/78636, PAGE_STUDY)
G=0.34719 (9811/28258, 14KJPN)
G=0.35030 (5871/16760, 8.3KJPN)
A=0.2859 (1831/6404, 1000G_30x)
A=0.2953 (1479/5008, 1000G)
A=0.1558 (698/4480, Estonian)
A=0.1458 (562/3854, ALSPAC)
A=0.1324 (491/3708, TWINSUK)
G=0.3430 (1005/2930, KOREAN)
A=0.3017 (569/1886, HapMap)
A=0.153 (153/998, GoNL)
G=0.371 (271/730, PRJEB37584)
A=0.208 (130/626, Chileans)
A=0.165 (99/600, NorthernSweden)
A=0.161 (86/534, MGP)
G=0.289 (92/318, SGDP_PRJ)
A=0.153 (33/216, Qatari)
G=0.292 (63/216, Vietnamese)
G=0.33 (10/30, Siberian)
Clinical Significance
Reported in ClinVar
Gene : Consequence
MYH9 : 3 Prime UTR 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 259096 G=0.850604 A=0.149396
European Sub 222674 G=0.864263 A=0.135737
African Sub 12346 G=0.89503 A=0.10497
African Others Sub 442 G=0.900 A=0.100
African American Sub 11904 G=0.89483 A=0.10517
Asian Sub 3840 G=0.2914 A=0.7086
East Asian Sub 3086 G=0.3156 A=0.6844
Other Asian Sub 754 G=0.192 A=0.808
Latin American 1 Sub 1166 G=0.8559 A=0.1441
Latin American 2 Sub 8646 G=0.7651 A=0.2349
South Asian Sub 376 G=0.609 A=0.391
Other Sub 10048 G=0.78901 A=0.21099


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 G=0.841970 A=0.158030
Allele Frequency Aggregator Total Global 254060 G=0.850260 A=0.149740
Allele Frequency Aggregator European Sub 219580 G=0.864154 A=0.135846
Allele Frequency Aggregator African Sub 11204 G=0.89522 A=0.10478
Allele Frequency Aggregator Other Sub 9248 G=0.7867 A=0.2133
Allele Frequency Aggregator Latin American 2 Sub 8646 G=0.7651 A=0.2349
Allele Frequency Aggregator Asian Sub 3840 G=0.2914 A=0.7086
Allele Frequency Aggregator Latin American 1 Sub 1166 G=0.8559 A=0.1441
Allele Frequency Aggregator South Asian Sub 376 G=0.609 A=0.391
gnomAD - Genomes Global Study-wide 140160 G=0.848965 A=0.151035
gnomAD - Genomes European Sub 75910 G=0.85358 A=0.14642
gnomAD - Genomes African Sub 42008 G=0.89478 A=0.10522
gnomAD - Genomes American Sub 13646 G=0.80874 A=0.19126
gnomAD - Genomes Ashkenazi Jewish Sub 3318 G=0.8550 A=0.1450
gnomAD - Genomes East Asian Sub 3128 G=0.3120 A=0.6880
gnomAD - Genomes Other Sub 2150 G=0.8181 A=0.1819
The PAGE Study Global Study-wide 78636 G=0.77378 A=0.22622
The PAGE Study AfricanAmerican Sub 32472 G=0.89221 A=0.10779
The PAGE Study Mexican Sub 10802 G=0.76727 A=0.23273
The PAGE Study Asian Sub 8314 G=0.3567 A=0.6433
The PAGE Study PuertoRican Sub 7912 G=0.8630 A=0.1370
The PAGE Study NativeHawaiian Sub 4532 G=0.4217 A=0.5783
The PAGE Study Cuban Sub 4230 G=0.8560 A=0.1440
The PAGE Study Dominican Sub 3826 G=0.8704 A=0.1296
The PAGE Study CentralAmerican Sub 2450 G=0.7698 A=0.2302
The PAGE Study SouthAmerican Sub 1982 G=0.7704 A=0.2296
The PAGE Study NativeAmerican Sub 1260 G=0.8143 A=0.1857
The PAGE Study SouthAsian Sub 856 G=0.575 A=0.425
14KJPN JAPANESE Study-wide 28258 G=0.34719 A=0.65281
8.3KJPN JAPANESE Study-wide 16760 G=0.35030 A=0.64970
1000Genomes_30x Global Study-wide 6404 G=0.7141 A=0.2859
1000Genomes_30x African Sub 1786 G=0.9009 A=0.0991
1000Genomes_30x Europe Sub 1266 G=0.8547 A=0.1453
1000Genomes_30x South Asian Sub 1202 G=0.5790 A=0.4210
1000Genomes_30x East Asian Sub 1170 G=0.3325 A=0.6675
1000Genomes_30x American Sub 980 G=0.813 A=0.187
1000Genomes Global Study-wide 5008 G=0.7047 A=0.2953
1000Genomes African Sub 1322 G=0.8994 A=0.1006
1000Genomes East Asian Sub 1008 G=0.3433 A=0.6567
1000Genomes Europe Sub 1006 G=0.8499 A=0.1501
1000Genomes South Asian Sub 978 G=0.585 A=0.415
1000Genomes American Sub 694 G=0.817 A=0.183
Genetic variation in the Estonian population Estonian Study-wide 4480 G=0.8442 A=0.1558
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 G=0.8542 A=0.1458
UK 10K study - Twins TWIN COHORT Study-wide 3708 G=0.8676 A=0.1324
KOREAN population from KRGDB KOREAN Study-wide 2930 G=0.3430 A=0.6570
HapMap Global Study-wide 1886 G=0.6983 A=0.3017
HapMap American Sub 766 G=0.667 A=0.333
HapMap African Sub 690 G=0.823 A=0.177
HapMap Asian Sub 254 G=0.343 A=0.657
HapMap Europe Sub 176 G=0.858 A=0.142
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 G=0.847 A=0.153
CNV burdens in cranial meningiomas Global Study-wide 730 G=0.371 A=0.629
CNV burdens in cranial meningiomas CRM Sub 730 G=0.371 A=0.629
Chileans Chilean Study-wide 626 G=0.792 A=0.208
Northern Sweden ACPOP Study-wide 600 G=0.835 A=0.165
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 G=0.839 A=0.161
SGDP_PRJ Global Study-wide 318 G=0.289 A=0.711
Qatari Global Study-wide 216 G=0.847 A=0.153
A Vietnamese Genetic Variation Database Global Study-wide 216 G=0.292 A=0.708
Siberian Global Study-wide 30 G=0.33 A=0.67
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 22 NC_000022.11:g.36281354G>A
GRCh37.p13 chr 22 NC_000022.10:g.36677400G>A
MYH9 RefSeqGene (LRG_567) NG_011884.2:g.111665C>T
Gene: MYH9, myosin heavy chain 9 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
MYH9 transcript NM_002473.6:c.*1314= N/A 3 Prime UTR 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.

Allele: A (allele ID: 338001 )
ClinVar Accession Disease Names Clinical Significance
RCV000274254.3 MYH9-related disorder Benign
RCV000366504.3 Autosomal dominant nonsyndromic hearing loss 17 Benign
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 G= A
GRCh38.p14 chr 22 NC_000022.11:g.36281354= NC_000022.11:g.36281354G>A
GRCh37.p13 chr 22 NC_000022.10:g.36677400= NC_000022.10:g.36677400G>A
MYH9 RefSeqGene (LRG_567) NG_011884.2:g.111665= NG_011884.2:g.111665C>T
MYH9 transcript NM_002473.6:c.*1314= NM_002473.6:c.*1314C>T
MYH9 transcript NM_002473.5:c.*1314= NM_002473.5:c.*1314C>T
MYH9 transcript NM_002473.4:c.*1314= NM_002473.4:c.*1314C>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#.

120 SubSNP, 22 Frequency, 2 ClinVar submissions
No Submitter Submission ID Date (Build)
1 WIAF ss2511 Sep 19, 2000 (36)
2 LEE ss1536208 Oct 04, 2000 (86)
3 CGAP-GAI ss4321973 Jan 04, 2002 (102)
4 LEE ss4424512 May 29, 2002 (106)
5 YUSUKE ss4474215 Jul 03, 2002 (106)
6 WI_SSAHASNP ss12529489 Jul 11, 2003 (116)
7 CSHL-HAPMAP ss16931690 Feb 27, 2004 (120)
8 CSHL-HAPMAP ss20145099 Feb 27, 2004 (120)
9 ABI ss41533778 Mar 15, 2006 (126)
10 KRIBB_YJKIM ss65824223 Nov 30, 2006 (127)
11 PERLEGEN ss69272997 May 17, 2007 (127)
12 AFFY ss76853216 Dec 06, 2007 (129)
13 CGM_KYOTO ss76870970 Dec 06, 2007 (129)
14 HGSV ss83260414 Dec 14, 2007 (130)
15 BGI ss103861911 Dec 01, 2009 (131)
16 KRIBB_YJKIM ss104807741 Feb 04, 2009 (130)
17 1000GENOMES ss112641573 Jan 25, 2009 (130)
18 GMI ss157173369 Dec 01, 2009 (131)
19 ILLUMINA ss160551644 Dec 01, 2009 (131)
20 ILLUMINA ss169131135 Jul 04, 2010 (132)
21 ILLUMINA ss173365280 Jul 04, 2010 (132)
22 BUSHMAN ss204087322 Jul 04, 2010 (132)
23 1000GENOMES ss228679273 Jul 14, 2010 (132)
24 1000GENOMES ss238069115 Jul 15, 2010 (132)
25 1000GENOMES ss244187205 Jul 15, 2010 (132)
26 GMI ss283635815 May 04, 2012 (137)
27 PJP ss292760676 May 09, 2011 (134)
28 ILLUMINA ss480582113 May 04, 2012 (137)
29 ILLUMINA ss480596573 May 04, 2012 (137)
30 ILLUMINA ss481420865 Sep 08, 2015 (146)
31 ILLUMINA ss485086535 May 04, 2012 (137)
32 ILLUMINA ss537095790 Sep 08, 2015 (146)
33 TISHKOFF ss566640420 Apr 25, 2013 (138)
34 SSMP ss662570797 Apr 25, 2013 (138)
35 ILLUMINA ss778870512 Sep 08, 2015 (146)
36 ILLUMINA ss782989541 Aug 21, 2014 (142)
37 ILLUMINA ss783950364 Sep 08, 2015 (146)
38 ILLUMINA ss832246319 Apr 01, 2015 (144)
39 ILLUMINA ss834331402 Sep 08, 2015 (146)
40 EVA-GONL ss995352431 Aug 21, 2014 (142)
41 JMKIDD_LAB ss1082659206 Aug 21, 2014 (142)
42 1000GENOMES ss1367167091 Aug 21, 2014 (142)
43 DDI ss1429256689 Apr 01, 2015 (144)
44 EVA_UK10K_ALSPAC ss1639996180 Apr 01, 2015 (144)
45 EVA_UK10K_TWINSUK ss1682990213 Apr 01, 2015 (144)
46 EVA_DECODE ss1699422384 Apr 01, 2015 (144)
47 EVA_MGP ss1711568405 Apr 01, 2015 (144)
48 EVA_SVP ss1713741240 Apr 01, 2015 (144)
49 ILLUMINA ss1752420694 Sep 08, 2015 (146)
50 HAMMER_LAB ss1809789042 Sep 08, 2015 (146)
51 WEILL_CORNELL_DGM ss1938919059 Feb 12, 2016 (147)
52 ILLUMINA ss1946589990 Feb 12, 2016 (147)
53 ILLUMINA ss1959979079 Feb 12, 2016 (147)
54 GENOMED ss1969272862 Jul 19, 2016 (147)
55 JJLAB ss2030231456 Sep 14, 2016 (149)
56 USC_VALOUEV ss2158850312 Dec 20, 2016 (150)
57 HUMAN_LONGEVITY ss2247334872 Dec 20, 2016 (150)
58 SYSTEMSBIOZJU ss2629613271 Nov 08, 2017 (151)
59 ILLUMINA ss2633878289 Nov 08, 2017 (151)
60 GRF ss2704602535 Nov 08, 2017 (151)
61 ILLUMINA ss2710957980 Nov 08, 2017 (151)
62 GNOMAD ss2974391919 Nov 08, 2017 (151)
63 AFFY ss2985854536 Nov 08, 2017 (151)
64 SWEGEN ss3019305304 Nov 08, 2017 (151)
65 ILLUMINA ss3022185920 Nov 08, 2017 (151)
66 BIOINF_KMB_FNS_UNIBA ss3028953013 Nov 08, 2017 (151)
67 CSHL ss3352838201 Nov 08, 2017 (151)
68 ILLUMINA ss3625802774 Oct 12, 2018 (152)
69 ILLUMINA ss3628534256 Oct 12, 2018 (152)
70 ILLUMINA ss3631829601 Oct 12, 2018 (152)
71 ILLUMINA ss3633273308 Oct 12, 2018 (152)
72 ILLUMINA ss3633989085 Oct 12, 2018 (152)
73 ILLUMINA ss3634867765 Oct 12, 2018 (152)
74 ILLUMINA ss3635673527 Oct 12, 2018 (152)
75 ILLUMINA ss3636563577 Oct 12, 2018 (152)
76 ILLUMINA ss3637425768 Oct 12, 2018 (152)
77 ILLUMINA ss3638382695 Oct 12, 2018 (152)
78 ILLUMINA ss3638382696 Oct 12, 2018 (152)
79 ILLUMINA ss3640575069 Oct 12, 2018 (152)
80 ILLUMINA ss3644800279 Oct 12, 2018 (152)
81 OMUKHERJEE_ADBS ss3646567033 Oct 12, 2018 (152)
82 ILLUMINA ss3652649279 Oct 12, 2018 (152)
83 EGCUT_WGS ss3685800655 Jul 13, 2019 (153)
84 EVA_DECODE ss3708202454 Jul 13, 2019 (153)
85 ILLUMINA ss3725968437 Jul 13, 2019 (153)
86 ACPOP ss3743935339 Jul 13, 2019 (153)
87 ILLUMINA ss3744206869 Jul 13, 2019 (153)
88 ILLUMINA ss3745167615 Jul 13, 2019 (153)
89 EVA ss3759384095 Jul 13, 2019 (153)
90 PAGE_CC ss3772091217 Jul 13, 2019 (153)
91 ILLUMINA ss3772663514 Jul 13, 2019 (153)
92 KHV_HUMAN_GENOMES ss3822547436 Jul 13, 2019 (153)
93 EVA ss3825970232 Apr 27, 2020 (154)
94 EVA ss3835992675 Apr 27, 2020 (154)
95 SGDP_PRJ ss3890548151 Apr 27, 2020 (154)
96 KRGDB ss3940945657 Apr 27, 2020 (154)
97 FSA-LAB ss3984235063 Apr 26, 2021 (155)
98 EVA ss3984760482 Apr 26, 2021 (155)
99 EVA ss3986087736 Apr 26, 2021 (155)
100 EVA ss4017880810 Apr 26, 2021 (155)
101 TOPMED ss5109248366 Apr 26, 2021 (155)
102 TOMMO_GENOMICS ss5232630899 Apr 26, 2021 (155)
103 1000G_HIGH_COVERAGE ss5311104239 Oct 16, 2022 (156)
104 EVA ss5316057116 Oct 16, 2022 (156)
105 EVA ss5441307387 Oct 16, 2022 (156)
106 HUGCELL_USP ss5502946163 Oct 16, 2022 (156)
107 EVA ss5512382380 Oct 16, 2022 (156)
108 1000G_HIGH_COVERAGE ss5618661472 Oct 16, 2022 (156)
109 SANFORD_IMAGENETICS ss5624503176 Oct 16, 2022 (156)
110 SANFORD_IMAGENETICS ss5664495707 Oct 16, 2022 (156)
111 TOMMO_GENOMICS ss5793751969 Oct 16, 2022 (156)
112 EVA ss5800041333 Oct 16, 2022 (156)
113 YY_MCH ss5818714265 Oct 16, 2022 (156)
114 EVA ss5822073918 Oct 16, 2022 (156)
115 EVA ss5847518451 Oct 16, 2022 (156)
116 EVA ss5847944313 Oct 16, 2022 (156)
117 EVA ss5853394929 Oct 16, 2022 (156)
118 EVA ss5881825326 Oct 16, 2022 (156)
119 EVA ss5959351508 Oct 16, 2022 (156)
120 EVA ss5979637477 Oct 16, 2022 (156)
121 1000Genomes NC_000022.10 - 36677400 Oct 12, 2018 (152)
122 1000Genomes_30x NC_000022.11 - 36281354 Oct 16, 2022 (156)
123 The Avon Longitudinal Study of Parents and Children NC_000022.10 - 36677400 Oct 12, 2018 (152)
124 Chileans NC_000022.10 - 36677400 Apr 27, 2020 (154)
125 Genetic variation in the Estonian population NC_000022.10 - 36677400 Oct 12, 2018 (152)
126 gnomAD - Genomes NC_000022.11 - 36281354 Apr 26, 2021 (155)
127 Genome of the Netherlands Release 5 NC_000022.10 - 36677400 Apr 27, 2020 (154)
128 HapMap NC_000022.11 - 36281354 Apr 27, 2020 (154)
129 KOREAN population from KRGDB NC_000022.10 - 36677400 Apr 27, 2020 (154)
130 Medical Genome Project healthy controls from Spanish population NC_000022.10 - 36677400 Apr 27, 2020 (154)
131 Northern Sweden NC_000022.10 - 36677400 Jul 13, 2019 (153)
132 The PAGE Study NC_000022.11 - 36281354 Jul 13, 2019 (153)
133 CNV burdens in cranial meningiomas NC_000022.10 - 36677400 Apr 26, 2021 (155)
134 Qatari NC_000022.10 - 36677400 Apr 27, 2020 (154)
135 SGDP_PRJ NC_000022.10 - 36677400 Apr 27, 2020 (154)
136 Siberian NC_000022.10 - 36677400 Apr 27, 2020 (154)
137 8.3KJPN NC_000022.10 - 36677400 Apr 26, 2021 (155)
138 14KJPN NC_000022.11 - 36281354 Oct 16, 2022 (156)
139 TopMed NC_000022.11 - 36281354 Apr 26, 2021 (155)
140 UK 10K study - Twins NC_000022.10 - 36677400 Oct 12, 2018 (152)
141 A Vietnamese Genetic Variation Database NC_000022.10 - 36677400 Jul 13, 2019 (153)
142 ALFA NC_000022.11 - 36281354 Apr 26, 2021 (155)
143 ClinVar RCV000274254.3 Oct 16, 2022 (156)
144 ClinVar RCV000366504.3 Oct 16, 2022 (156)
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)
rs7525 Oct 23, 2000 (87)
rs3197056 Jul 03, 2002 (106)
rs57513093 May 23, 2008 (130)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss83260414 NC_000022.8:35001899:G:A NC_000022.11:36281353:G:A (self)
ss112641573, ss204087322, ss283635815, ss292760676, ss480582113, ss1699422384, ss1713741240 NC_000022.9:35007345:G:A NC_000022.11:36281353:G:A (self)
80719373, 44650849, 271317, 31538903, 19896983, 48123051, 684165, 17220204, 310067, 20960981, 42565131, 11366666, 90600206, 44650849, 9851081, ss228679273, ss238069115, ss244187205, ss480596573, ss481420865, ss485086535, ss537095790, ss566640420, ss662570797, ss778870512, ss782989541, ss783950364, ss832246319, ss834331402, ss995352431, ss1082659206, ss1367167091, ss1429256689, ss1639996180, ss1682990213, ss1711568405, ss1752420694, ss1809789042, ss1938919059, ss1946589990, ss1959979079, ss1969272862, ss2030231456, ss2158850312, ss2629613271, ss2633878289, ss2704602535, ss2710957980, ss2974391919, ss2985854536, ss3019305304, ss3022185920, ss3352838201, ss3625802774, ss3628534256, ss3631829601, ss3633273308, ss3633989085, ss3634867765, ss3635673527, ss3636563577, ss3637425768, ss3638382695, ss3638382696, ss3640575069, ss3644800279, ss3646567033, ss3652649279, ss3685800655, ss3743935339, ss3744206869, ss3745167615, ss3759384095, ss3772663514, ss3825970232, ss3835992675, ss3890548151, ss3940945657, ss3984235063, ss3984760482, ss3986087736, ss4017880810, ss5232630899, ss5316057116, ss5441307387, ss5512382380, ss5624503176, ss5664495707, ss5800041333, ss5822073918, ss5847518451, ss5847944313, ss5959351508, ss5979637477 NC_000022.10:36677399:G:A NC_000022.11:36281353:G:A (self)
RCV000274254.3, RCV000366504.3, 106187407, 569999938, 2256011, 1312686, 127589073, 384357313, 8696423781, ss2247334872, ss3028953013, ss3708202454, ss3725968437, ss3772091217, ss3822547436, ss5109248366, ss5311104239, ss5502946163, ss5618661472, ss5793751969, ss5818714265, ss5853394929, ss5881825326 NC_000022.11:36281353:G:A NC_000022.11:36281353:G:A (self)
ss12529489, ss16931690, ss20145099 NT_011520.9:16015227:G:A NC_000022.11:36281353:G:A (self)
ss2511, ss1536208, ss4321973, ss4424512, ss4474215, ss41533778, ss65824223, ss69272997, ss76853216, ss76870970, ss103861911, ss104807741, ss157173369, ss160551644, ss169131135, ss173365280 NT_011520.12:16067968:G:A NC_000022.11:36281353:G:A (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 rs2481

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