rs951266
Orientation | minus |
Stabilized | minus |
Make rs951266(C;C) |
Make rs951266(C;T) |
Make rs951266(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 15 |
Position | 78586199 |
Gene | CHRNA5 |
is a | snp |
is | mentioned by |
dbSNP | rs951266 |
dbSNP (classic) | rs951266 |
ClinGen | rs951266 |
ebi | rs951266 |
HLI | rs951266 |
Exac | rs951266 |
Gnomad | rs951266 |
Varsome | rs951266 |
LitVar | rs951266 |
Map | rs951266 |
PheGenI | rs951266 |
Biobank | rs951266 |
1000 genomes | rs951266 |
hgdp | rs951266 |
ensembl | rs951266 |
geneview | rs951266 |
scholar | rs951266 |
rs951266 | |
pharmgkb | rs951266 |
gwascentral | rs951266 |
openSNP | rs951266 |
23andMe | rs951266 |
SNPshot | rs951266 |
SNPdbe | rs951266 |
MSV3d | rs951266 |
GWAS Ctlg | rs951266 |
GMAF | 0.1892 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Rs951266 | |
---|---|
PubMed | [PMID 18385738] |
Affy Probeset | SNP_A-4302972 |
Affy Orientation | same |
On GW 5.0 | |
Alleles A/B | C/T |
Ancestral | C |
Population | Caucasian(Europe) |
Allele | T |
Case Freq. | 0.4 |
Control Freq. | 0.34 |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | 1.30 |
Disease | Lung cancer (LC) |
rs951266 increases susceptibility to Lung cancer 1.28 times for heterozygotes (CT) and 1.80 times for homozygotes (TT) [PMID 18385676]
rs951266 increases susceptibility to Lung cancer 1.30 times for carriers of the T allele [PMID 18385738]
rs951266 increases susceptibility to Lung cancer 1.32 times for heterozygotes (CT) and 1.70 times for homozygotes (TT) [PMID 18385739]
rs951266 increases susceptibility to Peripheral arterial disease 1.21 times for heterozygotes (CT) and 1.41 times for homozygotes (TT) [PMID 18385739]
rs951266 increases susceptibility to Substance dependence, Nicotine 1.10 times for heterozygotes (CT) and 1.90 times for homozygotes (TT) [PMID 17135278]
rs951266 increases susceptibility to Substance dependence, Nicotine 1.39 times for heterozygotes (CT) and 1.97 times for homozygotes (TT) [PMID 18385739]
plos Risk Factors for Age-Dependent Nicotine Addiction
[PMID 17373692] No evidence for association between 19 cholinergic genes and bipolar disorder.
[PMID 18227835] Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking.
[PMID 18618000] A candidate gene approach identifies the CHRNA5-A3-B4 region as a risk factor for age-dependent nicotine addiction.
[PMID 18759969] In search of causal variants: refining disease association signals using cross-population contrasts.
[PMID 19330903] Gene by smoking interaction in hypertension: identification of a major quantitative trait locus on chromosome 15q for systolic blood pressure in Mexican-Americans.
[PMID 19443489] Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5.
[PMID 19706762] The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans.
[PMID 20808433] Associations of variants in CHRNA5/A3/B4 gene cluster with smoking behaviors in a Korean population.
[PMID 23196875] Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder