(A) Odds ratio (OR)/copy of risk allele (allelic model).
(B) heterozygote risk versus homozygote non-risk (genotypic model), random-effects analysis;
(C) homozygote risk versus homozygotes non-risk (genotypic model), random-effects analysis. Total n = 20,987; 14,232 multivessel disease, 6,755 single-vessel disease. Non-European ancestry cohorts were not included in the Bayesian analysis. Bayesian analysis showed no distinguishable differences between rs10757278/rs1333049 and rs2383206, for which the marginal effect estimate was nearly identical. CI = confidence interval; Bayesian = Bayesian model; CDCS = Coronary Disease Cohort Study; Cleveland GB = Cleveland GeneBank Study; D+L = DerSimonian and Laird random effects model; EmCB = Emory Cardiovascular Biobank; IHCS = Utah Intermountain Heart Collaborative Study; OHGS = Ottawa Heart Genomics Study; SAS = Southampton Atherosclerosis Study.