FLG and allergic disease: We examined the associations between 135 independent risk variants for allergic diseases identified in a recent GWAS9 and LCADs which we previously described in two independent birth cohorts.8 SNP rs61816761 (a protein‐truncating variant in FLG gene) and SNP rs921650 (within an intron of GSDMB) which were previously identified as having disease‐specific effects9 were differentially associated with distinct LCADs.