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 36
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 12
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 34
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs201893408 0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs121909574 0.724 0.400 6 10404509 missense variant T/A;C;G snv 4.6E-06 17
rs28933386 0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 14
rs138632121 0.776 0.400 16 3026140 missense variant T/A snv 1.7E-04 2.0E-04 13
rs200426926 0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 13
rs80338903 0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs267607144 0.716 0.360 12 109800665 missense variant C/T snv 17
rs138659167 0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs397507531 0.752 0.320 12 112473040 missense variant T/C;G snv 18
rs587777450 0.790 0.320 18 10671729 missense variant C/T snv 6
rs201108965 0.851 0.320 11 61393965 missense variant G/A;T snv 8.0E-06; 1.7E-04 5
rs587776934 0.851 0.320 19 18162974 missense variant G/A snv 3
rs199470477 1.000 0.320 10 75029027 frameshift variant CT/- delins 2
rs6467 0.925 0.320 6 32039081 missense variant C/A;G;T snv 0.64; 2.3E-03 2
rs180177035 0.752 0.280 7 140801502 missense variant T/C snv 35
rs869025195 0.790 0.280 1 155904493 missense variant T/G snv 11
rs138119149 0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 9
rs137852769 0.827 0.280 2 26195184 missense variant C/G snv 1.2E-03 1.0E-03 4
rs782138777 1.000 0.280 2 70958399 stop gained C/T snv 1.2E-05 1.4E-05 2
rs797045282 1.000 0.280 6 157206545 stop gained C/T snv 2
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18