Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80338903 0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 17
rs886039799 0.763 0.320 7 33273896 frameshift variant C/- del 17
rs137852832 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 17
rs549625604 0.752 0.280 12 76347713 frameshift variant -/A delins 6.0E-04 13
rs281865192 0.742 0.280 12 88101183 intron variant T/C snv 2.8E-04 11
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 8
rs121908175 0.790 0.160 16 56519791 stop gained G/C snv 5.2E-05 2.8E-05 8
rs397515360 0.807 0.160 8 86643781 frameshift variant G/- del 1.8E-03 8
rs2723341 0.807 0.160 15 71811481 splice acceptor variant A/C snv 5.3E-04 5.1E-04 8
rs755246809 0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 7
rs786205636 0.827 0.320 2 169493750 missense variant G/A snv 7
rs386834152 0.790 0.280 12 88114488 stop gained G/A snv 5.1E-05 4.9E-05 7
rs62645748 0.807 0.080 1 197434706 missense variant G/A snv 2.1E-04 2.2E-04 7
rs111033334 0.790 0.200 1 216247185 stop gained G/A snv 8.0E-06 7
rs111033364 0.807 0.200 1 215728232 stop gained C/T snv 9.2E-05 1.2E-04 7
rs281865377 0.807 0.080 1 94029447 frameshift variant G/-;GG delins 2.1E-05 6
rs61751392 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 6
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 6
rs76157638 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 6
rs886039800 0.851 0.240 15 72735944 frameshift variant G/- del 6
rs886039801 0.851 0.240 7 33388145 splice donor variant G/A snv 6
rs121909398 0.827 0.080 2 181558617 stop gained G/A;C snv 3.5E-04; 4.0E-06 6
rs398123538 0.882 0.200 3 121772605 frameshift variant TG/- delins 8.0E-05 7.0E-05 6