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
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057520002 0.695 0.360 17 7674242 missense variant 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
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 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
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 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
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11