Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
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
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21