Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 4
rs786205050 0.827 0.080 16 1212024 missense variant A/G snv 7.0E-06 4
rs121912667 0.851 0.200 17 7673766 missense variant T/A snv 3
rs587782529 0.851 0.200 17 7670700 missense variant G/A;C snv 3
rs63749993 0.882 0.200 2 47476424 missense variant T/G snv 3
rs730882029 0.882 0.200 17 7670685 stop gained G/A snv 3
rs1131691023 1.000 0.080 17 7675142 missense variant A/G;T snv 2
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs751477326 1.000 0.080 17 7675082 missense variant G/A;C snv 4.0E-06 1
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs375338359 0.882 0.200 17 7670684 missense variant C/G;T snv 8.0E-06 3
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs6471 0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 4