Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs880315 0.925 0.120 1 10736809 intron variant T/C snv 0.32 9