Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
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
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
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
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