GRM7 and Behcet disease: In the largest GWAS of BD to date, a SNP in an intergenic region flanking miR‐2113 on chromosome 6q16.1 was the eighth strongest finding.11 A gene‐based analysis of all known autosomal microRNAs using the same GWAS data found a significant association between nine microRNAs (including miR‐708) and BD.22 In another study, bioinformatic analysis suggested that the BD‐associated glutamate receptor‐7 gene (GRM7) 3ʹ UTR variant, rs56173829, might modulate the binding of several microRNAs, including miR‐4295, miR‐130a‐3p, and miR‐130b‐3p.23