At CUX2 the array-wide significant secondary signal (rs10849931-C; p-valueconditional = 1.05x10-7) was in weak LD with a previously described SNP for coronary artery disease (rs886126, r2 = 0.5 in 1000 Genomes EUR) [53] and weakly associated with the other previously described trait associations in the region (r2≤0.2). The gene discussed is CUX2; the disease is coronary artery disorder.