Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs587784347 0.742 0.280 22 38113561 missense variant G/A snv 8.0E-06 38
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs387907145 0.695 0.440 16 4800548 stop gained G/A snv 36
rs786205124 0.701 0.400 16 4798593 frameshift variant G/-;GGG delins 3.5E-05 35
rs137852981 0.752 0.480 2 144399104 stop gained G/A snv 30
rs374052333 0.763 0.320 3 132671032 stop gained C/G;T snv 4.0E-06 27
rs77078070 0.742 0.280 7 23165737 stop gained C/T snv 1.2E-05 1.4E-05 26
rs1555731819 0.807 0.200 19 35729980 missense variant G/T snv 26
rs375817528 0.776 0.160 11 65206824 splice region variant G/A snv 1.2E-04 1.2E-04 25
rs1555954284 0.752 0.360 X 41346607 missense variant C/T snv 24
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs387906799 0.742 0.200 2 240788118 missense variant G/A snv 19
rs886041091 0.807 0.120 9 84751990 missense variant A/G snv 18
rs1555454508 0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs1247665387 0.807 0.360 16 74774623 missense variant C/A snv 7.0E-06 14
rs776679653 0.827 0.200 9 86266174 missense variant C/T snv 4.2E-06 11