In Stage II, we sought additional evidence for associations in eight loci for MI (QKI, ODZ3, DGKB, FOXL1, CALCOCO2, BARD1, COL8A1, ATXN1) and eight loci for CHD (PAP2D, GPC5, CTNNA3, BARHL2, IGFBP3, LRFN2, ATXN1, SNCA) using four SNPs per locus, for a total of 60 SNPs in 15 loci (ATXN1 was associated with both MI and CHD). The gene discussed is CTNNA3; the disease is coronary artery disorder.