Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777893 0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs369160589 0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04 35
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
rs1555968941 0.752 0.280 12 2653847 missense variant G/A;C snv 31
rs1553920379 0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs34757931 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs1555745467 0.752 0.240 19 13262771 missense variant C/A snv 23
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
rs727502818 0.790 0.160 11 17772053 missense variant G/A snv 20
rs1555565492 0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs771379232 0.790 0.120 15 79845338 stop gained G/A snv 2.0E-05 3.5E-05 15
rs753635972 0.790 0.120 15 79845388 missense variant C/T snv 3.2E-05 2.1E-05 15
rs758946412 0.790 0.240 X 100407507 frameshift variant G/-;GG delins 12
rs869312825 0.827 0.120 1 1804548 start lost T/C snv 11
rs376103091 0.851 0.200 16 23544677 missense variant G/A snv 1.5E-04 2.0E-04 10
rs864309505 0.807 0.200 11 6615220 missense variant T/G snv 10
rs869312826 0.882 0.080 1 1787378 missense variant C/T snv 6
rs546151500 0.925 0.080 2 218643341 stop gained G/A;T snv 8.0E-06; 4.0E-06 5
rs1553798675 0.925 0.080 3 192335441 missense variant C/T snv 4
rs74315390 0.790 0.120 20 63439609 missense variant C/G;T snv 3
rs1065852 0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 2
rs121918622 0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 2
rs137852776 0.827 0.080 6 52452799 missense variant T/C snv 3.5E-03 2.4E-03 1