We check for significant deviation from BR = 1 in several gene sets: 44 genes associated with diseases with “autosomal recessive” in the name of the disease with at least 5 annotated variants in the Human Gene Mutation Database (HGMD), 37 genes associated with congenital hearing loss (HL) and found only with AR mode of inheritance in a clinical genetics lab, and 1348 genes with Clinical Genomic Database (CGD) AR annotations [38–40]. Here, AR is linked to Hodgkins lymphoma.