Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs763733111 0.925 0.120 9 125149801 missense variant G/A snv 4.0E-06 2
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 6
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 14
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30