Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs1557036768 0.708 0.320 X 53647390 missense variant C/T snv 44
rs1178187217 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 38
rs201943194 0.683 0.480 7 21710596 stop gained C/T snv 8.5E-05 8.4E-05 38
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs1232880706 0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs387907145 0.695 0.440 16 4800548 stop gained G/A snv 36
rs1364709483 0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05 36
rs369160589 0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04 35
rs786205124 0.701 0.400 16 4798593 frameshift variant G/-;GGG delins 3.5E-05 35
rs1009298200 0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06 34
rs1555452127 0.742 0.400 16 5079078 missense variant T/C snv 34
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs1060505041 0.716 0.400 19 13136099 missense variant C/A;T snv 34
rs1569518070 0.752 0.480 21 45989088 inframe deletion AAC/- del 33
rs875989800 0.732 0.480 22 23833670 inframe deletion AGA/- delins 33
rs1555968941 0.752 0.280 12 2653847 missense variant G/A;C snv 31