grch37-exome-variants-gnomad-v1
SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples.
SNV and INDEL varaints from 125,748 exomes in the gnomAD dataset version 2.1.1 in bcf format. The file constains all subsets of non-neuro, non-cancer, controls-only, and non-TOPMed samples.