Disease: Hemophilia B
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852247
F9
0.925 0.080 X 139560852 missense variant G/A snv 3
rs137852249
F9
0.882 0.080 X 139561566 missense variant G/A snv 3
rs137852254
F9
0.882 0.080 X 139561710 missense variant C/T snv 3
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv 3
rs137852435
F8
0.925 0.080 X 154931641 missense variant G/A snv 1.7E-05 3
rs28935499
F8
0.925 0.080 X 154966525 missense variant C/A;T snv 3
rs387906475
F9
0.882 0.080 X 139530843 missense variant G/A snv 3
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06 3
rs137852228
F9
0.925 0.080 X 139537145 missense variant G/A snv 5.5E-06 2
rs137852238
F9
0.925 0.080 X 139551113 missense variant G/A snv 5.5E-06 9.5E-06 2
rs137852257
F9
0.925 0.080 X 139561754 missense variant G/A snv 2
rs137852259
F9
0.925 0.080 X 139561821 missense variant G/A snv 2
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv 2
rs137852394
F8
0.925 0.080 X 154992996 missense variant C/T snv 2
rs137852405
F8
0.925 0.080 X 154969405 missense variant A/G snv 2
rs137852414
F8
0.925 0.080 X 154961120 stop gained C/A;T snv 2
rs137852416
F8
0.925 0.080 X 154957073 missense variant G/A snv 2
rs137852424
F8
0.925 0.080 X 154953991 stop gained G/A;T snv 1.1E-05 2
rs137852428
F8
0.925 0.080 X 154953961 missense variant G/A snv 2.2E-05 9.5E-06 2
rs137852436
F8
0.925 0.080 X 154931623 missense variant C/T snv 5.5E-06 2
rs137852461
F8
0.925 0.080 X 154863151 missense variant C/T snv 2
rs137852465
F8
0.925 0.080 X 154863124 missense variant C/A;T snv 5.5E-06 2
rs137852469
F8
0.925 0.080 X 154860588 missense variant C/A snv 2
rs137852472
F8
0.925 0.080 X 154837697 missense variant G/A snv 2
rs1490417405
F8
0.925 0.080 X 154903950 missense variant C/T snv 9.5E-06 2