Source: CURATED

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: rs137852228
rs137852228
F9
0.925 0.080 X 139537145 missense variant G/A snv 5.5E-06
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852238
rs137852238
F9
0.925 0.080 X 139551113 missense variant G/A snv 5.5E-06 9.5E-06
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852247
rs137852247
F9
0.925 0.080 X 139560852 missense variant G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852249
rs137852249
F9
0.882 0.080 X 139561566 missense variant G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852254
rs137852254
F9
0.882 0.080 X 139561710 missense variant C/T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852257
rs137852257
F9
0.925 0.080 X 139561754 missense variant G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs137852259
rs137852259
F9
0.925 0.080 X 139561821 missense variant G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 1 2019 2019
dbSNP: rs1557271042
rs1557271042
F8
1.000 0.080 X 154837622 missense variant C/T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs137852360
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 2 2011 2013
dbSNP: rs137852354
rs137852354
F8
1.000 0.080 X 154837677 stop gained G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs137852474
rs137852474
F8
1.000 0.080 X 154837685 missense variant C/G;T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 22 1989 2013
dbSNP: rs137852473
rs137852473
F8
1.000 0.080 X 154837686 missense variant G/A;C snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 22 1989 2013
dbSNP: rs137852472
rs137852472
F8
0.925 0.080 X 154837697 missense variant G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 22 1989 2013
dbSNP: rs137852374
rs137852374
F8
1.000 0.080 X 154837698 missense variant G/A snv 5.5E-06
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.810 1.000 2 2009 2013
dbSNP: rs387906466
rs387906466
F8
1.000 0.080 X 154837735 frameshift variant GATTT/- delins
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs137852471
rs137852471
F8
1.000 0.080 X 154860467 stop gained G/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs782717799
rs782717799
F8
1.000 0.080 X 154860497 missense variant A/T snv 5.5E-06
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 20 1989 2002
dbSNP: rs387906465
rs387906465
F8
1.000 0.080 X 154860537 frameshift variant CT/- del
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs137852470
rs137852470
F8
1.000 0.080 X 154860538 missense variant T/C snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 22 1989 2013
dbSNP: rs782479558
rs782479558
F8
1.000 0.080 X 154860580 missense variant A/G;T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 20 1989 2002
dbSNP: rs137852469
rs137852469
F8
0.925 0.080 X 154860588 missense variant C/A snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 22 1989 2013
dbSNP: rs387906464
rs387906464
F8
1.000 0.080 X 154861742 frameshift variant C/- delins
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 0
dbSNP: rs137852358
rs137852358
F8
0.882 0.080 X 154861758 missense variant C/A;T snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.810 1.000 2 2010 2013
dbSNP: rs137852355
rs137852355
F8
1.000 0.080 X 154861759 stop gained G/A;C snv
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.800 1.000 2 2011 2013
dbSNP: rs782548763
rs782548763
F8
0.925 0.080 X 154861783 missense variant C/G snv 5.5E-06
CUI: C0019069
Disease: Hemophilia A
Hemophilia A
0.700 1.000 20 1989 2002