Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
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
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs869312824 0.827 0.200 1 1804565 missense variant A/G snv 14
rs1556914274 0.790 0.440 X 53537626 missense variant G/A snv 13
rs759317757 0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 12
rs188675529 0.827 0.240 16 67842794 missense variant C/G;T snv 1.6E-03 6.0E-04 11
rs776679653 0.827 0.200 9 86266174 missense variant C/T snv 4.2E-06 11
rs753242774 0.882 0.120 3 47848237 missense variant C/A;T snv 9
rs1555696625 0.851 0.360 19 13025409 missense variant G/A snv 7