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
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs737866 1.000 0.080 22 19942586 intron variant T/A;C snv 2
rs1280296282 1.000 0.080 20 1982967 missense variant T/C snv 4.0E-06 1.4E-05 1