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
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs1565679039 0.701 0.400 12 47983399 stop gained T/A snv 45
rs1560755661 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 44
rs1555386022 0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs1555038111 0.701 0.480 11 118478153 stop gained T/G snv 37
rs1232880706 0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs1009298200 0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06 34
rs1555452127 0.742 0.400 16 5079078 missense variant T/C snv 34
rs543860009 0.742 0.320 2 178589003 stop gained G/A;T snv 33
rs878854378 0.742 0.320 2 178533657 inframe deletion GTT/- delins 33
rs137854889 0.742 0.440 1 40290871 frameshift variant T/-;TT delins 31
rs151344517 0.742 0.320 18 12337505 missense variant C/T snv 31
rs1294950721 0.807 0.360 20 10645355 splice donor variant C/A;T snv 7.0E-06 27
rs137854539 0.716 0.520 20 58903703 missense variant C/T snv 27
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs864321670 0.763 0.320 10 95633012 missense variant C/T snv 24
rs1563221666 0.882 0.120 8 22162694 missense variant C/T snv 14
rs1421405659 0.851 0.360 12 101642529 missense variant T/C;G snv 13
rs1344172059 0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 12
rs1554199368 0.827 0.160 5 177256956 missense variant C/T snv 12
rs180177039 0.851 0.160 7 140778006 missense variant T/A;C;G snv 12
rs1555564126 0.882 0.320 17 44853306 frameshift variant C/- delins 9
rs1569162748 0.925 0.120 X 13767142 frameshift variant AAATT/- del 7