nominally significantp<0.001
While not all previously known DR variants were identified at genome-wide significance in our analyses, we observed an excess of nominally significant associations at these loci (p<0.001, Table B in S1 File ).
While not all previously known DR variants were identified at genome-wide significance in our analyses, we observed an excess of nominally significant associations at these loci (p<0.001, Table B in S1 File ).
An inflation of p-values compared to permuted phenotypes was observed only within the tail end of highly significant SNPs.