Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519919 0.851 0.160 2 15942195 missense variant C/T snv 5
rs876659675 0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs1057519995 0.807 0.240 17 7674200 missense variant T/A snv 8
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 11
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs1057519992 0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 14
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 16
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs864622237 0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 19
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20