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 35
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
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 24
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
rs1057519959 0.882 0.200 11 66063028 missense variant A/C snv 4
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
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
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37