The scope of inherited burden for disease predisposition across diverse populations variant set

The data presented as a TSV table contains a list of all variants of 3970 PanelApp disease genes from 730,947 individuals from gnomAD 4.1.0. The columns are: Variant identifier (chromosome, position, reference allele, alternate allele), Gene name, Variant effect based on Ensembl VEP, AAVC classification & criteria, Allele count & number information for all eight genetic ancestry groups. AAVC can be accessed through https://aavc.bilkent.edu.tr/.