highly significantP = 1.27 × 10 −7
The association at rs2735591 is highly significant in the combined validation samples ( P = 1.27 × 10 −7 , OR = 1.27), even after correction for all the 4363 SNPs tested in the current study ( P corrected = 5.54 × 10 −4 ) and surpassed the genome-wide significance threshold ( P = 1.03 × 10 −9 , OR = 1.24) in the combined GWAS and two independent validation series, consisting of a total of 3148 cases and 7843 controls (Table 2 ).