Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs483352697 0.695 0.480 17 7674944 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
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 9
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37