Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.

We observed a weak trend towards lower MAF ( P =0.042, Wilcoxon test, Supplementary Table 1 ) for the best fine-mapping SNP (Immunochip experiment) versus the lead SNP from our 2010 tag SNP GWAS (measuring MAF in a subset of samples genotyped in both datasets).

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