Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs180177135 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs137853011 0.763 0.280 22 28695219 missense variant G/A snv 4.9E-04 2.6E-04 16
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 16
rs41293497 0.724 0.440 13 32340037 stop gained C/A;G;T snv 4.0E-06; 2.0E-05 14
rs80358721 0.724 0.320 13 32339320 stop gained C/A;G;R snv 4.2E-06 14
rs80358920 0.732 0.400 13 32346841 stop gained C/G;T snv 14
rs41293459 0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 12
rs80358814 0.742 0.440 13 32340212 stop gained G/T snv 8.0E-06 12
rs80358972 0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 12
rs80359200 0.752 0.320 13 32394726 stop gained C/A;G snv 8.0E-06 12
rs80359473 0.807 0.400 13 32339288 frameshift variant GAAA/- delins 12
rs118203998 0.790 0.400 16 23603471 stop gained G/C;T snv 1.6E-05; 4.0E-06 11
rs180177132 0.790 0.280 16 23621362 stop gained C/T snv 6.0E-05 2.1E-05 11
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 11
rs28897756 0.752 0.440 13 32379913 splice region variant G/A;C;T snv 4.0E-06 11
rs80356898 0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 11
rs80357382 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 11
rs80358435 0.752 0.440 13 32319154 stop gained G/C;T snv 4.0E-06; 4.0E-06 11
rs80359212 0.763 0.320 13 32394814 stop gained C/T snv 1.2E-05 4.2E-05 11
rs397507404 0.763 0.320 13 32370955 splice acceptor variant G/A;T snv 10
rs41293511 0.763 0.320 13 32363369 missense variant G/A;C snv 7.0E-06 10
rs55770810 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 10
rs80357522 0.776 0.280 17 43093570 frameshift variant TTTT/-;TT;TTT;TTTTT delins 7.0E-06 10
rs80358391 0.763 0.320 13 32319109 stop gained G/A;T snv 4.0E-06 10