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
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
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
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
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
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs1057519986 0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987 0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519988 0.776 0.240 17 7673812 missense variant A/C;G;T snv 10