Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
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
rs1057519757 0.882 0.120 5 68293310 missense variant G/A;C snv 5
rs1057519887 0.925 0.040 7 55154128 missense variant GC/AA;AT mnv 3
rs1057519888 0.925 0.080 7 55143386 missense variant A/G snv 3
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
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 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
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
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
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs1057519995 0.807 0.240 17 7674200 missense variant T/A snv 9