Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs180177035 0.752 0.280 7 140801502 missense variant T/C snv 35
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 34
rs201893408 0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs80338903 0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs138659167 0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs397507531 0.752 0.320 12 112473040 missense variant T/C;G snv 18
rs398123009 0.790 0.200 11 66211206 missense variant C/T snv 7.0E-06 17
rs121909574 0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06 17
rs267607144 0.716 0.360 12 109800665 missense variant C/T snv 17
rs28933386 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 14
rs672601370 0.790 0.160 2 240775863 missense variant G/A snv 13
rs200426926 0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 13
rs138632121 0.776 0.400 16 3026140 missense variant T/A snv 1.7E-04 2.0E-04 13
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 12
rs869025195 0.790 0.280 1 155904493 missense variant T/G snv 11
rs137852813 0.807 0.200 2 39051202 missense variant A/C;G snv 11
rs387907329 0.827 0.200 X 49075573 stop gained G/A;T snv 5.5E-06 10
rs138119149 0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 9
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 8
rs34002892 0.851 0.200 12 101753470 frameshift variant GA/- delins 5.1E-04 3.5E-04 8
rs386834236
GAA
0.882 0.120 17 80104542 intron variant T/G snv 3.4E-03 3.8E-03 6
rs111033178 0.851 0.200 11 77190108 missense variant G/A snv 7.5E-05 5.6E-05 6