Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;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
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 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
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 14
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 13
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12