Autosomal variants do not associate with GVHD. The number of patient-specific missense variants (A) as well as known unrestricted (B) and HLA-restricted (C) MiHAs is comparable in the acute GVHD and non-GVHD groups. (D) Known, HLA-restricted MiHAs ordered by log-odds ratio (acute GVHD to non-GVHD). SNP, single-nucleotide polymorphism.