Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs1126809 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs764146326 0.662 0.480 17 7673779 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 24
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22