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
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
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
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs4964057 0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs6350 0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3