Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555743003 0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs1557036768 0.708 0.320 X 53647390 missense variant C/T snv 44
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs1553655558 0.752 0.360 2 229830831 frameshift variant A/- delins 43
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs1569518070 0.752 0.480 21 45989088 inframe deletion AAC/- del 33
rs1557781252 0.742 0.320 1 153816414 stop gained G/A snv 33
rs1555575860 0.732 0.240 16 70496367 missense variant C/G;T snv 31
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs1085307845 0.752 0.320 6 79025582 missense variant G/T snv 21
rs1441937959 0.763 0.280 15 82240555 missense variant T/C snv 8.2E-06 20
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs869312824 0.827 0.200 1 1804565 missense variant A/G snv 14
rs141322087 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs1554032789 0.925 0.160 5 37048547 missense variant T/A snv 13
rs1344172059 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 12
rs869312823 0.882 0.080 1 1806509 missense variant T/C snv 9
rs796051881 0.807 0.440 12 7202274 frameshift variant -/A delins 9
rs1426488816 0.827 0.160 9 26913948 splice acceptor variant C/T snv 8.0E-06 9
rs869312697 0.882 0.400 6 157207241 stop gained C/T snv 8
rs372392424 0.882 0.240 4 523849 missense variant C/T snv 6.7E-05 7.7E-05 8