Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894231 0.776 0.360 11 533467 missense variant C/G;T snv 9
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519893 0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
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
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44