Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752746786 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30
rs1057518345 0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs1991517 0.752 0.240 14 81144239 missense variant G/C snv 0.90 0.91 13
rs121917893 0.807 0.160 X 71167508 missense variant C/T snv 10
rs104894110 0.776 0.280 9 97854108 missense variant C/T snv 8
rs189261858 0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 8
rs1057518950
TPO
0.851 0.280 2 1484815 missense variant C/T snv 7
rs2076738
TG
0.807 0.200 8 132906843 missense variant T/C snv 1.6E-05 7.0E-06 6
rs748793969 0.827 0.120 15 45106327 missense variant G/A;T snv 3.2E-05; 6.8E-05 5
rs2076739
TG
0.827 0.200 8 132971804 missense variant T/A snv 5
rs763679435 0.882 0.120 14 81143883 stop gained C/T snv 4.0E-06 2.1E-05 4
rs370991693 0.851 0.160 8 133017916 missense variant C/A snv 4.4E-05 2.8E-05 4
rs104893656 0.851 0.120 2 113246826 missense variant T/G snv 4
rs191759494 0.882 0.120 15 45108159 missense variant C/G;T snv 4.0E-06; 1.4E-04 3
rs530719719 0.882 0.120 15 45101228 frameshift variant ACGA/- delins 2.9E-03 2.6E-03 3
rs4774518 0.925 0.120 15 45117274 stop gained C/G;T snv 1.4E-04; 1.7E-02 3
rs765367813 0.882 0.120 14 81143640 missense variant C/A;T snv 4.0E-06 3
rs121908866 0.882 0.120 14 81143695 stop gained G/A snv 1.1E-04 2.0E-04 3
rs119472026 0.925 0.120 15 45108887 stop gained G/A;C snv 6.8E-05 2
rs181461079 0.925 0.120 15 45103960 missense variant C/A;T snv 4.1E-04; 1.2E-04 2
rs746165975 0.925 0.120 15 45106254 frameshift variant -/T delins 4.0E-06 2
rs121909175 0.925 0.120 19 17877840 stop gained C/A snv 7.0E-06 2
rs898275076
TG
0.925 0.120 8 133022135 missense variant G/A snv 7.0E-06 2
rs121908082
TPO
0.925 0.120 2 1487841 stop gained C/A;G;T snv 4.0E-06; 4.0E-06; 1.2E-05 2
rs121908086
TPO
0.925 0.120 2 1493976 missense variant G/A snv 1.2E-05 7.0E-06 2