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
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs199469465 0.672 0.560 16 30737343 stop gained C/A;T snv 50
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs1555727493 0.742 0.480 19 35718020 frameshift variant -/GGCGGGCGGCGGC delins 46
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 45
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs866294686 0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs587782995 0.708 0.360 5 140114480 missense variant T/C snv 42
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs587784347 0.742 0.280 22 38113561 missense variant G/A snv 8.0E-06 38
rs1559931177 0.827 0.120 3 49047207 stop gained G/A snv 34
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
rs875989800 0.732 0.480 22 23833670 inframe deletion AGA/- delins 33
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
rs373145711 0.732 0.520 20 32433408 stop gained C/T snv 2.0E-05 2.8E-05 25
rs1555257073 0.827 0.120 13 28672407 frameshift variant AT/- delins 25
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs886043994 0.776 0.400 20 32433355 frameshift variant GT/- delins 21