Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28935490 1.000 0.160 X 101398432 missense variant C/A;T snv 3.0E-03; 5.4E-06 3
rs104894845 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs149391489 1.000 0.160 X 101401803 missense variant T/C snv 3.3E-04 4.2E-04 1
rs148158093 0.925 0.200 X 101403828 missense variant G/A snv 2.2E-04 4.0E-04 3
rs140329381 1.000 0.160 X 101398504 missense variant T/A;C snv 1.6E-04 1
rs104894833 0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11
rs782449839 1.000 0.160 X 101397903 missense variant C/G snv 8.2E-05 1.9E-05 1
rs111422676 1.000 0.160 X 101398011 missense variant C/T snv 5.5E-05 1.3E-04 1
rs727503950 1.000 0.160 X 101400712 missense variant A/G snv 1.1E-05 1.9E-05 1
rs869312163 1.000 0.160 X 101398032 missense variant C/G;T snv 1.1E-05 1
rs372966991 1.000 0.160 X 101403845 missense variant C/A;T snv 1.1E-05 1
rs869312344 1.000 0.160 X 101400700 missense variant C/G;T snv 5.5E-06 1
rs782197638 1.000 0.160 X 101403819 missense variant C/T snv 5.5E-06 1
rs869312162 1.000 0.160 X 101398044 missense variant G/C snv 5.5E-06 1
rs782598150 1.000 0.160 X 101398021 missense variant C/A;G snv 5.5E-06 1
rs104894849 1.000 0.160 X 101398004 stop gained A/G;T snv 5.5E-06 1
rs28935197 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs190347120 1.000 0.160 X 101398796 missense variant C/A;T snv 5.5E-06 1
rs104894844 1.000 0.160 X 101397907 stop gained C/A;T snv 5.5E-06 1
rs397515874 1.000 0.160 X 101398857 missense variant C/G;T snv 5.5E-06 1
rs869312389 1.000 0.160 X 101398867 frameshift variant TT/-;T delins 5.4E-06 1
rs104894828 0.882 0.160 X 101398467 missense variant C/A;T snv 3
rs104894851 0.925 0.200 X 101398920 stop gained G/T snv 3
rs104894852 0.925 0.200 X 101397871 missense variant T/C snv 3
rs199473684 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 3