Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22