Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
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
rs1057524820 0.776 0.280 12 51765746 missense variant G/A;T snv 33
rs28934907 0.732 0.320 X 154032268 missense variant G/A;C snv 30
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs1553920379 0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs727502818 0.790 0.160 11 17772053 missense variant G/A snv 26
rs267608327 0.763 0.200 X 154030631 splice acceptor variant CCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGT/- delins 25
rs1448259271 0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs796052686 0.776 0.280 7 66638394 missense variant G/A snv 1.2E-05 22
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs1057518843 0.790 0.240 14 87988523 missense variant C/T snv 19
rs1057524157 0.776 0.200 11 686962 missense variant A/C;T snv 19
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs1555955296 0.742 0.320 X 18628716 stop gained C/T snv 17
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 17
rs1057516264 0.776 0.280 11 6614968 frameshift variant C/-;CC delins 13
rs1555582065 0.827 0.160 17 44212851 missense variant C/T snv 13
rs748787734 0.827 0.240 19 6495437 missense variant G/A;C snv 1.2E-05 13
rs1554901898 0.776 0.280 11 6616858 frameshift variant A/- delins 12
rs1566785990 0.851 0.120 14 77026534 missense variant A/G snv 12
rs397507478 0.790 0.440 7 140777014 missense variant C/A snv 12