Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1554700718 0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs796052505 0.724 0.440 5 162095551 missense variant G/A;C snv 57
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs875989800 0.732 0.480 22 23833670 inframe deletion AGA/- delins 33
rs1331463984 0.701 0.240 16 2176350 missense variant G/A snv 33
rs137852981 0.752 0.480 2 144399104 stop gained G/A snv 30
rs397517148 0.776 0.200 2 39023128 missense variant C/T snv 27
rs77078070 0.742 0.280 7 23165737 stop gained C/T snv 1.2E-05 1.4E-05 26
rs1554208945 0.752 0.240 6 87260207 missense variant A/C snv 26
rs1569509136 0.708 0.400 X 53647576 splice acceptor variant T/C snv 24
rs886043994 0.776 0.400 20 32433355 frameshift variant GT/- delins 21
rs387906846 0.807 0.280 1 26773716 stop gained C/G;T snv 19
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16
rs1060503383 0.882 0.200 6 33441318 stop gained C/T snv 14
rs112795301 0.776 0.160 3 70972634 stop gained G/A snv 13
rs1554317931 0.851 0.080 7 42045460 frameshift variant G/- delins 11
rs1554691658 0.807 0.240 9 95459653 frameshift variant C/GGGTCCACAACATCT delins 11
rs1114167291 0.790 0.280 16 89281225 stop gained C/A snv 10
rs1057516044 0.851 0.240 12 21913005 missense variant A/G snv 9
rs371011047 0.882 0.120 11 103120982 stop gained G/T snv 2.8E-05 9
rs764926983 0.882 0.120 11 103287559 synonymous variant G/A snv 1.2E-05 9