Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9