Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131692230 0.807 0.160 X 19353124 missense variant A/G snv 9
rs746800707 0.851 0.160 20 36240388 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 8
rs200473652 0.807 0.200 2 209819105 missense variant G/C snv 1.4E-03 1.6E-03 7
rs886041094 0.807 0.200 2 209941379 missense variant G/A snv 1.9E-05 2.1E-05 7
rs1057518963 0.851 0.200 X 68210239 missense variant A/G snv 6
rs1114167296 0.827 0.160 X 34656995 missense variant C/G snv 6
rs61751035 0.882 0.160 1 213242186 missense variant G/A snv 2.4E-05 1.4E-05 6
rs1057519439 1.000 0.120 2 195787135 missense variant A/G snv 5
rs1114167297 0.851 0.160 10 32019912 missense variant T/C snv 5
rs1114167298 0.882 0.120 3 6861849 missense variant T/C snv 7.0E-06 5
rs146539065 0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs1560755661 0.701 0.480 4 106171094 splice donor variant CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- delins 44
rs786205124 0.701 0.400 16 4798593 frameshift variant G/-;GGG delins 3.5E-05 35
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs1553212868 0.807 0.280 1 151406264 frameshift variant G/- delins 17
rs1223073957 0.827 0.240 19 49835897 frameshift variant C/- delins 1.2E-05 1.4E-05 12
rs1057518934 0.851 0.240 15 28211095 frameshift variant G/- delins 8
rs1559307932 0.807 0.360 2 231737190 frameshift variant -/C ins 8
rs1114167295 0.827 0.160 X 54812169 frameshift variant C/- del 6
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs776969714 0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1555493029 0.851 0.240 16 23406263 splice acceptor variant C/A snv 10
rs1555497604 0.851 0.240 16 23452993 start lost A/G snv 10
rs1562846694 0.763 0.320 7 100643252 inframe deletion TTCGCTCCACGCACT/- delins 32