Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1650420 1.000 0.080 16 10174473 intron variant T/C snv 0.58 2