Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 16
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 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
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs587780073 0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 19
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs730882025 0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22