Rs588765

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Orientationplus
Make rs588765(C;C)
Make rs588765(C;T)
Make rs588765(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position78573083
GeneCHRNA5
is asnp
is mentioned by
dbSNPrs588765
PheGenIrs588765
nextbiors588765
hapmaprs588765
1000 genomesrs588765
hgdprs588765
ensemblrs588765
gopubmedrs588765
geneviewrs588765
scholarrs588765
googlers588765
pharmgkbrs588765
gwascentralrs588765
openSNPrs588765
23andMers588765
23andMe allrs588765
SNP Nexus

SNPshotrs588765
SNPdbers588765
MSV3drs588765
GMAF0.2759
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19706806] A Novel Polymorphism rs1329149 of CYP2E1 and a Known Polymorphism rs671 of ALDH2 of Alcohol Metabolizing Enzymes Are Associated with Colorectal Cancer in a Southwestern Chinese Population

[PMID 19706810] Variants Weakly Correlated with CHRNA5 D398N Polymorphism Should be Considered in Transcriptional Deregulation at the 15q25 Locus Associated with Lung Cancer Risk

[PMID 20700436OA-icon.png] Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD

OMIM118505
DescCHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 5; CHRNA5
Variant
Relatedalso
[PMID 19029397OA-icon.png] Nicotinic receptor gene variants influence susceptibility to heavy smoking.


[PMID 19443489OA-icon.png] Risk for nicotine dependence and lung cancer is conferred by mRNA expression levels and amino acid change in CHRNA5.


[PMID 19706762OA-icon.png] The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans.


[PMID 23249876OA-icon.png] Nicotinic acetylcholine receptor variation and response to smoking cessation therapies


[PMID 22884254] Association of nicotine dependence susceptibility gene, CHRNA5, with Parkinson's disease age at onset: gene and smoking status interaction.


[PMID 23011884] Functional effect of polymorphisms in 15q25 locus on CHRNA5 mRNA, bulky DNA adducts and TP53 mutations.


[PMID 23404318OA-icon.png] Interpreting joint SNP analysis results: when are two distinct signals really two distinct signals?