SNPs are shown with P<0.05 in the replication set.

All P-values are two-sided. All odds ratios are shown with respect to the minor allele. Combined P-values were computed with Fishers combined P-value technique implemented in HaploView. Loci reported for the first time in this current study are annotated. Positions shown are based on Build 36 of the human genome. Minor allele frequencies are shown for the controls in the discovery cohort.