Candidate gene results for the 4 CVD outcomes provided suggestive confirmation of prior associations reported for ALOX5AP (23 SNPs, 7 with p < 0.05 by GEE or FBAT), GJA4 (14 SNPs, 6 with p < 0.05), MEF2A (5 SNPs, 2 with p < 0.05), and PCSK9 (11 SNPs, 3 with p < 0.05) in relation to CHD risk. This evidence concerns the gene ALOX5AP and coronary artery disorder.