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. 2013 Aug 13;3(8):e290. doi: 10.1038/tp.2013.63

Table 2. Top genetic variants associated with cigarettes per day in the STOMP Consortium (P-value <5 × 10−7; David et al. 18) included in the Detroit Neighborhood Health Study Genetic Risk Score (n=399).

SNP Chromosome BP position Nearby genes Alleles Coded AF Effect size
rs2036527 15 76638670 CHRNA5 A/G 0.22 0.040
rs667282a 15 76650527 CHRNA5 C/T 0.29 0.033
rs3101457 1 242599837 C1orf100 A/G 0.75 0.041
rs938682 15 76683602 CHRNA3 A/G 0.71 0.033
rs547843 15 23975140 LOC503519 C/G 0.65 −0.035
rs3813570a 15 76619887 PSMA4 C/T 0.26 0.033

Abbreviations: AF, allele frequency; BP, base pair position; CHRNA5=cholinergic receptor, nicotinic, alpha 5; C1orf100=uncharacterized chromosome 1 open reading frame; CHRNA3=cholinergic receptor, nicotinic, alpha 3; LOC503519=uncharacterized; PSMA4=proteasome (prosome, macropain) subunit, alpha type 4; SNP, single-nucleotide polymorphism.

a

Note: When the original STOMP (David et al.18) SNP was not available for analysis in the DNHS, a proxy SNP (r2>0.9) was used in its place; rs667282 served as a proxy for rs667282 (r2=0.924), rs7163730 served as a proxy for rs3813570 (r2=0.916).