Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18