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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.

rs11118555

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:207767508 (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
T>A
Variation Type
SNV Single Nucleotide Variation
Frequency
A=0.091738 (24282/264690, TOPMED)
A=0.093196 (13058/140114, GnomAD)
A=0.08144 (6408/78684, PAGE_STUDY) (+ 20 more)
A=0.09067 (2562/28256, 14KJPN)
A=0.10318 (2167/21002, ALFA)
A=0.09069 (1520/16760, 8.3KJPN)
A=0.0843 (540/6404, 1000G_30x)
A=0.0823 (412/5008, 1000G)
A=0.1292 (579/4480, Estonian)
A=0.1038 (400/3854, ALSPAC)
A=0.1170 (434/3708, TWINSUK)
A=0.0832 (243/2922, KOREAN)
A=0.122 (122/998, GoNL)
A=0.096 (75/780, PRJEB37584)
A=0.142 (85/600, NorthernSweden)
A=0.118 (63/534, MGP)
A=0.064 (21/330, HapMap)
A=0.046 (10/216, Qatari)
A=0.042 (9/216, Vietnamese)
T=0.451 (46/102, SGDP_PRJ)
A=0.07 (3/40, GENOME_DK)
T=0.44 (8/18, Siberian)
A=0.0 (0/8, Ancient Sardinia)
Clinical Significance
Reported in ClinVar
Gene : Consequence
CD46 : 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 21002 T=0.89682 A=0.10318
European Sub 16364 T=0.88310 A=0.11690
African Sub 2946 T=0.9786 A=0.0214
African Others Sub 114 T=0.991 A=0.009
African American Sub 2832 T=0.9781 A=0.0219
Asian Sub 112 T=0.955 A=0.045
East Asian Sub 86 T=0.94 A=0.06
Other Asian Sub 26 T=1.00 A=0.00
Latin American 1 Sub 146 T=0.890 A=0.110
Latin American 2 Sub 610 T=0.846 A=0.154
South Asian Sub 98 T=0.87 A=0.13
Other Sub 726 T=0.913 A=0.087


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 T=0.908262 A=0.091738
gnomAD - Genomes Global Study-wide 140114 T=0.906804 A=0.093196
gnomAD - Genomes European Sub 75856 T=0.88184 A=0.11816
gnomAD - Genomes African Sub 42026 T=0.97751 A=0.02249
gnomAD - Genomes American Sub 13628 T=0.82976 A=0.17024
gnomAD - Genomes Ashkenazi Jewish Sub 3324 T=0.8881 A=0.1119
gnomAD - Genomes East Asian Sub 3128 T=0.9223 A=0.0777
gnomAD - Genomes Other Sub 2152 T=0.9001 A=0.0999
The PAGE Study Global Study-wide 78684 T=0.91856 A=0.08144
The PAGE Study AfricanAmerican Sub 32506 T=0.97284 A=0.02716
The PAGE Study Mexican Sub 10810 T=0.85467 A=0.14533
The PAGE Study Asian Sub 8318 T=0.9137 A=0.0863
The PAGE Study PuertoRican Sub 7918 T=0.8517 A=0.1483
The PAGE Study NativeHawaiian Sub 4534 T=0.9491 A=0.0509
The PAGE Study Cuban Sub 4224 T=0.8973 A=0.1027
The PAGE Study Dominican Sub 3828 T=0.9224 A=0.0776
The PAGE Study CentralAmerican Sub 2450 T=0.8127 A=0.1873
The PAGE Study SouthAmerican Sub 1980 T=0.7944 A=0.2056
The PAGE Study NativeAmerican Sub 1260 T=0.8762 A=0.1238
The PAGE Study SouthAsian Sub 856 T=0.909 A=0.091
14KJPN JAPANESE Study-wide 28256 T=0.90933 A=0.09067
Allele Frequency Aggregator Total Global 21002 T=0.89682 A=0.10318
Allele Frequency Aggregator European Sub 16364 T=0.88310 A=0.11690
Allele Frequency Aggregator African Sub 2946 T=0.9786 A=0.0214
Allele Frequency Aggregator Other Sub 726 T=0.913 A=0.087
Allele Frequency Aggregator Latin American 2 Sub 610 T=0.846 A=0.154
Allele Frequency Aggregator Latin American 1 Sub 146 T=0.890 A=0.110
Allele Frequency Aggregator Asian Sub 112 T=0.955 A=0.045
Allele Frequency Aggregator South Asian Sub 98 T=0.87 A=0.13
8.3KJPN JAPANESE Study-wide 16760 T=0.90931 A=0.09069
1000Genomes_30x Global Study-wide 6404 T=0.9157 A=0.0843
1000Genomes_30x African Sub 1786 T=0.9916 A=0.0084
1000Genomes_30x Europe Sub 1266 T=0.8697 A=0.1303
1000Genomes_30x South Asian Sub 1202 T=0.9235 A=0.0765
1000Genomes_30x East Asian Sub 1170 T=0.9231 A=0.0769
1000Genomes_30x American Sub 980 T=0.818 A=0.182
1000Genomes Global Study-wide 5008 T=0.9177 A=0.0823
1000Genomes African Sub 1322 T=0.9917 A=0.0083
1000Genomes East Asian Sub 1008 T=0.9276 A=0.0724
1000Genomes Europe Sub 1006 T=0.8748 A=0.1252
1000Genomes South Asian Sub 978 T=0.921 A=0.079
1000Genomes American Sub 694 T=0.820 A=0.180
Genetic variation in the Estonian population Estonian Study-wide 4480 T=0.8708 A=0.1292
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 T=0.8962 A=0.1038
UK 10K study - Twins TWIN COHORT Study-wide 3708 T=0.8830 A=0.1170
KOREAN population from KRGDB KOREAN Study-wide 2922 T=0.9168 A=0.0832
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 T=0.878 A=0.122
CNV burdens in cranial meningiomas Global Study-wide 780 T=0.904 A=0.096
CNV burdens in cranial meningiomas CRM Sub 780 T=0.904 A=0.096
Northern Sweden ACPOP Study-wide 600 T=0.858 A=0.142
Medical Genome Project healthy controls from Spanish population Spanish controls Study-wide 534 T=0.882 A=0.118
HapMap Global Study-wide 330 T=0.936 A=0.064
HapMap African Sub 120 T=1.000 A=0.000
HapMap American Sub 120 T=0.875 A=0.125
HapMap Asian Sub 90 T=0.93 A=0.07
Qatari Global Study-wide 216 T=0.954 A=0.046
A Vietnamese Genetic Variation Database Global Study-wide 216 T=0.958 A=0.042
SGDP_PRJ Global Study-wide 102 T=0.451 A=0.549
The Danish reference pan genome Danish Study-wide 40 T=0.93 A=0.07
Siberian Global Study-wide 18 T=0.44 A=0.56
Ancient Sardinia genome-wide 1240k capture data generation and analysis Global Study-wide 8 T=1.0 A=0.0
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.207767508T>A
GRCh37.p13 chr 1 NC_000001.10:g.207940853T>A
CD46 RefSeqGene (LRG_155) NG_009296.1:g.20452T>A
Gene: CD46, CD46 molecule (plus strand)
Molecule type Change Amino acid[Codon] SO Term
CD46 transcript variant a NM_002389.4:c.857-99T>A N/A Intron Variant
CD46 transcript variant d NM_153826.4:c.857-271T>A N/A Intron Variant
CD46 transcript variant n NM_172350.3:c.856+313T>A N/A Intron Variant
CD46 transcript variant c NM_172351.3:c.857-271T>A N/A Intron Variant
CD46 transcript variant e NM_172352.3:c.856+313T>A N/A Intron Variant
CD46 transcript variant f NM_172353.3:c.856+313T>A N/A Intron Variant
CD46 transcript variant i NM_172355.3:c.857-271T>A N/A Intron Variant
CD46 transcript variant j NM_172356.3:c.857-271T>A N/A Intron Variant
CD46 transcript variant k NM_172357.3:c.856+313T>A N/A Intron Variant
CD46 transcript variant m NM_172358.3:c.857-271T>A N/A Intron Variant
CD46 transcript variant b NM_172359.3:c.857-99T>A N/A Intron Variant
CD46 transcript variant l NM_172361.3:c.856+313T>A N/A Intron Variant
CD46 transcript variant X2 XM_011509563.3:c.857-99T>A N/A Intron Variant
CD46 transcript variant X1 XM_047420888.1:c.857-99T>A N/A Intron Variant
CD46 transcript variant X3 XM_047420894.1:c.857-271T…

XM_047420894.1:c.857-271T>A

 		N/A Intron Variant
CD46 transcript variant X4 XM_047420901.1:c.857-271T…

XM_047420901.1:c.857-271T>A

 		N/A Intron Variant
CD46 transcript variant X5 XM_047420909.1:c.856+313T…

XM_047420909.1:c.856+313T>A

 		N/A Intron 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: 1279384 )
ClinVar Accession Disease Names Clinical Significance
RCV001714082.1 not provided 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 T= A
GRCh38.p14 chr 1 NC_000001.11:g.207767508= NC_000001.11:g.207767508T>A
GRCh37.p13 chr 1 NC_000001.10:g.207940853= NC_000001.10:g.207940853T>A
CD46 RefSeqGene (LRG_155) NG_009296.1:g.20452= NG_009296.1:g.20452T>A
CD46 transcript variant a NM_002389.4:c.857-99= NM_002389.4:c.857-99T>A
CD46 transcript variant d NM_153826.3:c.857-271= NM_153826.3:c.857-271T>A
CD46 transcript variant d NM_153826.4:c.857-271= NM_153826.4:c.857-271T>A
CD46 transcript variant n NM_172350.2:c.856+313= NM_172350.2:c.856+313T>A
CD46 transcript variant n NM_172350.3:c.856+313= NM_172350.3:c.856+313T>A
CD46 transcript variant c NM_172351.2:c.857-271= NM_172351.2:c.857-271T>A
CD46 transcript variant c NM_172351.3:c.857-271= NM_172351.3:c.857-271T>A
CD46 transcript variant e NM_172352.2:c.856+313= NM_172352.2:c.856+313T>A
CD46 transcript variant e NM_172352.3:c.856+313= NM_172352.3:c.856+313T>A
CD46 transcript variant f NM_172353.2:c.856+313= NM_172353.2:c.856+313T>A
CD46 transcript variant f NM_172353.3:c.856+313= NM_172353.3:c.856+313T>A
CD46 transcript variant i NM_172355.3:c.857-271= NM_172355.3:c.857-271T>A
CD46 transcript variant j NM_172356.3:c.857-271= NM_172356.3:c.857-271T>A
CD46 transcript variant k NM_172357.3:c.856+313= NM_172357.3:c.856+313T>A
CD46 transcript variant m NM_172358.3:c.857-271= NM_172358.3:c.857-271T>A
CD46 transcript variant b NM_172359.2:c.857-99= NM_172359.2:c.857-99T>A
CD46 transcript variant b NM_172359.3:c.857-99= NM_172359.3:c.857-99T>A
CD46 transcript variant l NM_172361.2:c.856+313= NM_172361.2:c.856+313T>A
CD46 transcript variant l NM_172361.3:c.856+313= NM_172361.3:c.856+313T>A
CD46 transcript variant X2 XM_011509563.3:c.857-99= XM_011509563.3:c.857-99T>A
CD46 transcript variant X1 XM_047420888.1:c.857-99= XM_047420888.1:c.857-99T>A
CD46 transcript variant X3 XM_047420894.1:c.857-271= XM_047420894.1:c.857-271T>A
CD46 transcript variant X4 XM_047420901.1:c.857-271= XM_047420901.1:c.857-271T>A
CD46 transcript variant X5 XM_047420909.1:c.856+313= XM_047420909.1:c.856+313T>A
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#.

76 SubSNP, 23 Frequency, 1 ClinVar submissions
No Submitter Submission ID Date (Build)
1 CSHL-HAPMAP ss19109947 Feb 27, 2004 (120)
2 CSHL-HAPMAP ss19840281 Feb 27, 2004 (120)
3 PERLEGEN ss24617558 Sep 20, 2004 (123)
4 ABI ss44036464 Mar 14, 2006 (126)
5 PGA-UW-FHCRC ss52051787 Oct 14, 2006 (127)
6 SI_EXO ss52068644 Oct 14, 2006 (127)
7 HUMANGENOME_JCVI ss99282016 Feb 06, 2009 (130)
8 1000GENOMES ss108898890 Jan 23, 2009 (130)
9 ENSEMBL ss161211667 Dec 01, 2009 (131)
10 ILLUMINA ss171047292 Jul 04, 2010 (132)
11 1000GENOMES ss230875659 Jul 14, 2010 (132)
12 1000GENOMES ss238493140 Jul 15, 2010 (132)
13 GMI ss276192199 May 04, 2012 (137)
14 PJP ss290721235 May 09, 2011 (134)
15 ILLUMINA ss410891901 Sep 17, 2011 (135)
16 ILLUMINA ss536676007 Sep 08, 2015 (146)
17 SSMP ss648655897 Apr 25, 2013 (138)
18 EVA-GONL ss976075758 Aug 21, 2014 (142)
19 JMKIDD_LAB ss1068550639 Aug 21, 2014 (142)
20 1000GENOMES ss1294395982 Aug 21, 2014 (142)
21 EVA_GENOME_DK ss1574633167 Apr 01, 2015 (144)
22 EVA_DECODE ss1585471016 Apr 01, 2015 (144)
23 EVA_UK10K_ALSPAC ss1602001690 Apr 01, 2015 (144)
24 EVA_UK10K_TWINSUK ss1644995723 Apr 01, 2015 (144)
25 EVA_MGP ss1710941954 Apr 01, 2015 (144)
26 WEILL_CORNELL_DGM ss1919302679 Feb 12, 2016 (147)
27 ILLUMINA ss1958352035 Feb 12, 2016 (147)
28 GENOMED ss1966956675 Jul 19, 2016 (147)
29 JJLAB ss2020171992 Sep 14, 2016 (149)
30 USC_VALOUEV ss2148201785 Dec 20, 2016 (150)
31 HUMAN_LONGEVITY ss2169562517 Dec 20, 2016 (150)
32 SYSTEMSBIOZJU ss2624594568 Nov 08, 2017 (151)
33 GRF ss2698193534 Nov 08, 2017 (151)
34 GNOMAD ss2765507499 Nov 08, 2017 (151)
35 AFFY ss2985536651 Nov 08, 2017 (151)
36 SWEGEN ss2988346542 Nov 08, 2017 (151)
37 ILLUMINA ss3021174230 Nov 08, 2017 (151)
38 BIOINF_KMB_FNS_UNIBA ss3023845923 Nov 08, 2017 (151)
39 CSHL ss3343881930 Nov 08, 2017 (151)
40 ILLUMINA ss3637810160 Oct 11, 2018 (152)
41 OMUKHERJEE_ADBS ss3646252548 Oct 11, 2018 (152)
42 URBANLAB ss3646873034 Oct 11, 2018 (152)
43 ILLUMINA ss3651518180 Oct 11, 2018 (152)
44 EGCUT_WGS ss3656303387 Jul 12, 2019 (153)
45 EVA_DECODE ss3688505528 Jul 12, 2019 (153)
46 ILLUMINA ss3725100152 Jul 12, 2019 (153)
47 ACPOP ss3727806002 Jul 12, 2019 (153)
48 EVA ss3747255599 Jul 12, 2019 (153)
49 PAGE_CC ss3770867763 Jul 12, 2019 (153)
50 KHV_HUMAN_GENOMES ss3800262459 Jul 12, 2019 (153)
51 EVA ss3826610626 Apr 25, 2020 (154)
52 SGDP_PRJ ss3850767490 Apr 25, 2020 (154)
53 KRGDB ss3896068849 Apr 25, 2020 (154)
54 FSA-LAB ss3983961733 Apr 25, 2021 (155)
55 FSA-LAB ss3983961734 Apr 25, 2021 (155)
56 EVA ss3984470902 Apr 25, 2021 (155)
57 EVA ss3984847619 Apr 25, 2021 (155)
58 EVA ss4016958488 Apr 25, 2021 (155)
59 TOPMED ss4481359832 Apr 25, 2021 (155)
60 TOMMO_GENOMICS ss5148150226 Apr 25, 2021 (155)
61 EVA ss5237280566 Apr 25, 2021 (155)
62 1000G_HIGH_COVERAGE ss5245577704 Oct 12, 2022 (156)
63 EVA ss5324388287 Oct 12, 2022 (156)
64 HUGCELL_USP ss5446034998 Oct 12, 2022 (156)
65 EVA ss5506165363 Oct 12, 2022 (156)
66 1000G_HIGH_COVERAGE ss5519562734 Oct 12, 2022 (156)
67 EVA ss5623918245 Oct 12, 2022 (156)
68 SANFORD_IMAGENETICS ss5624227960 Oct 12, 2022 (156)
69 SANFORD_IMAGENETICS ss5627322249 Oct 12, 2022 (156)
70 TOMMO_GENOMICS ss5675831067 Oct 12, 2022 (156)
71 YY_MCH ss5801582088 Oct 12, 2022 (156)
72 EVA ss5833172980 Oct 12, 2022 (156)
73 EVA ss5847571670 Oct 12, 2022 (156)
74 EVA ss5911717650 Oct 12, 2022 (156)
75 EVA ss5939152958 Oct 12, 2022 (156)
76 EVA ss5979302622 Oct 12, 2022 (156)
77 1000Genomes NC_000001.10 - 207940853 Oct 11, 2018 (152)
78 1000Genomes_30x NC_000001.11 - 207767508 Oct 12, 2022 (156)
79 The Avon Longitudinal Study of Parents and Children NC_000001.10 - 207940853 Oct 11, 2018 (152)
80 Genetic variation in the Estonian population NC_000001.10 - 207940853 Oct 11, 2018 (152)
81 The Danish reference pan genome NC_000001.10 - 207940853 Apr 25, 2020 (154)
82 gnomAD - Genomes NC_000001.11 - 207767508 Apr 25, 2021 (155)
83 Genome of the Netherlands Release 5 NC_000001.10 - 207940853 Apr 25, 2020 (154)
84 HapMap NC_000001.11 - 207767508 Apr 25, 2020 (154)
85 KOREAN population from KRGDB NC_000001.10 - 207940853 Apr 25, 2020 (154)
86 Medical Genome Project healthy controls from Spanish population NC_000001.10 - 207940853 Apr 25, 2020 (154)
87 Northern Sweden NC_000001.10 - 207940853 Jul 12, 2019 (153)
88 The PAGE Study NC_000001.11 - 207767508 Jul 12, 2019 (153)
89 Ancient Sardinia genome-wide 1240k capture data generation and analysis NC_000001.10 - 207940853 Apr 25, 2021 (155)
90 CNV burdens in cranial meningiomas NC_000001.10 - 207940853 Apr 25, 2021 (155)
91 Qatari NC_000001.10 - 207940853 Apr 25, 2020 (154)
92 SGDP_PRJ NC_000001.10 - 207940853 Apr 25, 2020 (154)
93 Siberian NC_000001.10 - 207940853 Apr 25, 2020 (154)
94 8.3KJPN NC_000001.10 - 207940853 Apr 25, 2021 (155)
95 14KJPN NC_000001.11 - 207767508 Oct 12, 2022 (156)
96 TopMed NC_000001.11 - 207767508 Apr 25, 2021 (155)
97 UK 10K study - Twins NC_000001.10 - 207940853 Oct 11, 2018 (152)
98 A Vietnamese Genetic Variation Database NC_000001.10 - 207940853 Jul 12, 2019 (153)
99 ALFA NC_000001.11 - 207767508 Apr 25, 2021 (155)
100 ClinVar RCV001714082.1 Oct 12, 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)
rs17186995 Oct 07, 2004 (123)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
ss108898890, ss276192199, ss290721235, ss1585471016 NC_000001.9:206007475:T:A NC_000001.11:207767507:T:A (self)
5241397, 2887306, 2041635, 1857881, 1260492, 3246243, 58706, 1090867, 73546, 20220, 1344609, 2784470, 718139, 6119533, 2887306, 622897, ss230875659, ss238493140, ss536676007, ss648655897, ss976075758, ss1068550639, ss1294395982, ss1574633167, ss1602001690, ss1644995723, ss1710941954, ss1919302679, ss1958352035, ss1966956675, ss2020171992, ss2148201785, ss2624594568, ss2698193534, ss2765507499, ss2985536651, ss2988346542, ss3021174230, ss3343881930, ss3637810160, ss3646252548, ss3651518180, ss3656303387, ss3727806002, ss3747255599, ss3826610626, ss3850767490, ss3896068849, ss3983961733, ss3983961734, ss3984470902, ss3984847619, ss4016958488, ss5148150226, ss5237280566, ss5324388287, ss5506165363, ss5623918245, ss5624227960, ss5627322249, ss5833172980, ss5847571670, ss5939152958, ss5979302622 NC_000001.10:207940852:T:A NC_000001.11:207767507:T:A (self)
RCV001714082.1, 7088669, 37768921, 253512, 89232, 9668171, 44966167, 9156362362, ss2169562517, ss3023845923, ss3646873034, ss3688505528, ss3725100152, ss3770867763, ss3800262459, ss4481359832, ss5245577704, ss5446034998, ss5519562734, ss5675831067, ss5801582088, ss5911717650 NC_000001.11:207767507:T:A NC_000001.11:207767507:T:A (self)
ss19109947, ss19840281 NT_021877.16:1403959:T:A NC_000001.11:207767507:T:A (self)
ss52068644 NT_021877.17:1403959:T:A NC_000001.11:207767507:T:A (self)
ss24617558, ss44036464, ss52051787, ss99282016, ss161211667, ss171047292, ss410891901 NT_167186.1:1458631:T:A NC_000001.11:207767507:T: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 rs11118555

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