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
rs1057519699 3 179218315 missense variant G/A snv 2
rs1057519724 1.000 0.080 10 87933236 missense variant G/A;T snv 3
rs1057519738 0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 10
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519890 0.807 0.200 17 39723966 missense variant T/A snv 8
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
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
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 10
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
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13