nominally significantp <0.01
Table S1 presents an overview of the most nominally significant SNPs ( p <0.01) in the regions that have been reported for CAD.
Table S1 presents an overview of the most nominally significant SNPs ( p <0.01) in the regions that have been reported for CAD.
Recent GWAS and their replications that have established highly significant associations of variants with MI and/or CAD are predominantly based on populations of European [11] , [12] , [13] , Eastern Asian [11] , [14] , [15] , and more recently, South Asian descent [16] .