Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs1569355102 0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs199469465 0.672 0.560 16 30737343 stop gained C/A;T snv 50
rs1565679039 0.701 0.400 12 47983399 stop gained T/A snv 45
rs866294686 0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs1553655558 0.752 0.360 2 229830831 frameshift variant A/- delins 43
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs180177135 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs1555731819 0.807 0.200 19 35729980 missense variant G/T snv 26
rs1554208945 0.752 0.240 6 87260207 missense variant A/C snv 26
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs121918487 0.716 0.440 10 121517378 missense variant C/A;G;T snv 25
rs1569509136 0.708 0.400 X 53647576 splice acceptor variant T/C snv 24
rs137854466 0.724 0.320 15 48411280 stop gained G/A;C snv 4.0E-05; 8.0E-06 23
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs886043994 0.776 0.400 20 32433355 frameshift variant GT/- delins 21
rs864309486 0.763 0.320 6 24777262 stop gained A/T snv 21
rs1135401778 0.752 0.400 17 67854315 frameshift variant T/- del 20
rs864309487 0.763 0.280 6 24777279 frameshift variant TCAA/- delins 20
rs1566785444 0.827 0.200 14 77025671 frameshift variant C/- delins 20
rs794727931 0.790 0.240 11 78112692 missense variant A/C snv 19
rs1558939623 0.732 0.480 2 174824479 missense variant C/T snv 19