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Smoking is a leading global cause of disease and mortality. We established the Oxford-GlaxoSmithKline study (Ox-GSK) to perform a genome-wide meta-analysis of SNP association with smoking-related behavioral traits. Our final data set included 41,150 individuals drawn from 20 disease, population and control cohorts. Our analysis confirmed an effect on smoking quantity at a locus on 15q25 (P = 9.45 x 10(-19)) that includes CHRNA5, CHRNA3 and CHRNB4, three genes encoding neuronal nicotinic acetylcholine receptor subunits. We used data from the 1000 Genomes project to investigate the region using imputation, which allowed for analysis of virtually all common SNPs in the region and offered a fivefold increase in marker density over HapMap2 (ref. 2) as an imputation reference panel. Our fine-mapping approach identified a SNP showing the highest significance, rs55853698, located within the promoter region of CHRNA5. Conditional analysis also identified a secondary locus (rs6495308) in CHRNA3.

Original publication

DOI

10.1038/ng.572

Type

Journal article

Journal

Nat Genet

Publication Date

05/2010

Volume

42

Pages

436 - 440

Keywords

Adult, Aged, Alleles, Chromosome Mapping, Chromosomes, Human, Pair 15, Cohort Studies, Female, Genetic Markers, Genome, Human, Humans, Male, Middle Aged, Models, Genetic, Neurons, Polymorphism, Single Nucleotide, Receptors, Nicotinic, Smoking