Replicated associations that were genome-wide significant in their own right in FinnGen (class 1) included for instance that between rs10774625 (nearest gene: SH2B3/ATXN2) and coeliac disease (p = 1.3×10−6 in UK Biobank; p = 2.1×10−10 in FinnGen). This evidence concerns the gene SH2B3 and celiac disease.