Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs766182641
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2003 2003
dbSNP: rs773084111
rs773084111
AK3
1.000 0.080 9 4713088 missense variant C/A snv 8.0E-06 7.0E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2011 2011
dbSNP: rs17231520
rs17231520
0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs563558831
rs563558831
0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs549591993
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs137852358
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852360
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852394
rs137852394
F8
0.925 0.080 X 154992996 missense variant C/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852405
rs137852405
F8
0.925 0.080 X 154969405 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852414
rs137852414
F8
0.925 0.080 X 154961120 stop gained C/A;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852416
rs137852416
F8
0.925 0.080 X 154957073 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852424
rs137852424
F8
0.925 0.080 X 154953991 stop gained G/A;T snv 1.1E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852428
rs137852428
F8
0.925 0.080 X 154953961 missense variant G/A snv 2.2E-05 9.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852435
rs137852435
F8
0.925 0.080 X 154931641 missense variant G/A snv 1.7E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852436
rs137852436
F8
0.925 0.080 X 154931623 missense variant C/T snv 5.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852461
rs137852461
F8
0.925 0.080 X 154863151 missense variant C/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852465
rs137852465
F8
0.925 0.080 X 154863124 missense variant C/A;T snv 5.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852469
rs137852469
F8
0.925 0.080 X 154860588 missense variant C/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs137852472
rs137852472
F8
0.925 0.080 X 154837697 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs1490417405
rs1490417405
F8
0.925 0.080 X 154903950 missense variant C/T snv 9.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs28933675
rs28933675
F8
0.925 0.080 X 154904867 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs28935499
rs28935499
F8
0.925 0.080 X 154966525 missense variant C/A;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs369414658
rs369414658
F8
0.925 0.080 X 154902077 missense variant C/T snv 2.7E-05 8.5E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs375241473
rs375241473
F8
0.925 0.080 X 154966603 missense variant T/C snv 6.5E-05 6.6E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs387906450
rs387906450
F8
0.925 0.080 X 154930153 frameshift variant T/-;TT delins
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019