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
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs1557043622 0.695 0.400 X 48909843 missense variant C/A snv 46
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs146539065 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs755246809 0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 7