nominally significantP <0.05
We first used the set-based test feature in PLINK with 100 000 permutations to identify up to 5 SNPs in each gene that were independent of one another ( r 2 <0.5) and nominally significant ( P <0.05).
We first used the set-based test feature in PLINK with 100 000 permutations to identify up to 5 SNPs in each gene that were independent of one another ( r 2 <0.5) and nominally significant ( P <0.05).