Gene: F8 ×
Source: CURATED ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs944567323
rs944567323
F8
1 1.000 0.080 X 154999538 missense variant A/C;G snv 0.700 0
dbSNP: rs886039906
rs886039906
F8
3 1.000 0.080 X 154929022 frameshift variant -/TTGGTTAT ins 3.3E-05 0.700 0
dbSNP: rs868988809
rs868988809
F8
1 1.000 0.080 X 154969469 missense variant C/T snv 0.700 0
dbSNP: rs782733685
rs782733685
F8
1 1.000 0.080 X 154957140 synonymous variant C/A snv 1.1E-05 0.700 0
dbSNP: rs782717799
rs782717799
F8
1 1.000 0.080 X 154860497 missense variant A/T snv 5.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs782657516
rs782657516
F8
1 1.000 0.080 X 154956961 missense variant T/C snv 2.2E-05 0.800 1.000 22 1989 2013
dbSNP: rs782641941
rs782641941
F8
1 1.000 0.080 X 154863152 missense variant G/A snv 5.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs782548763
rs782548763
F8
1 0.925 0.080 X 154861783 missense variant C/G snv 5.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs782485864
rs782485864
F8
1 1.000 0.080 X 154961149 missense variant G/C snv 5.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs782481755
rs782481755
F8
1 1.000 0.080 X 154997012 missense variant G/A snv 0.700 1.000 20 1989 2002
dbSNP: rs782479558
rs782479558
F8
1 1.000 0.080 X 154860580 missense variant A/G;T snv 0.700 1.000 20 1989 2002
dbSNP: rs782318401
rs782318401
F8
1 1.000 0.080 X 154930950 missense variant G/C snv 6.7E-05 5.7E-05 0.700 1.000 20 1989 2002
dbSNP: rs782193428
rs782193428
F8
1 1.000 0.080 X 154957009 missense variant A/G snv 5.5E-06 2.8E-05 0.700 1.000 20 1989 2002
dbSNP: rs782127226
rs782127226
F8
1 0.925 0.080 X 154928962 missense variant C/A snv 4.4E-05 0.700 1.000 20 1989 2002
dbSNP: rs782098979
rs782098979
F8
1 1.000 0.080 X 154861866 missense variant C/A snv 1.1E-05 0.700 1.000 20 1989 2002
dbSNP: rs781974394
rs781974394
F8
1 1.000 0.080 X 154999496 missense variant G/C snv 2.7E-05 0.700 1.000 20 1989 2002
dbSNP: rs781954986
rs781954986
F8
1 1.000 0.080 X 154966679 missense variant C/T snv 1.9E-04 9.5E-06 0.700 1.000 20 1989 2002
dbSNP: rs397514036
rs397514036
F8
1 1.000 0.080 X 154928965 frameshift variant T/-;TT delins 0.700 0
dbSNP: rs387906466
rs387906466
F8
1 1.000 0.080 X 154837735 frameshift variant GATTT/- delins 0.700 0
dbSNP: rs387906465
rs387906465
F8
1 1.000 0.080 X 154860537 frameshift variant CT/- del 0.700 0
dbSNP: rs387906464
rs387906464
F8
1 1.000 0.080 X 154861742 frameshift variant C/- delins 0.700 0
dbSNP: rs387906463
rs387906463
F8
1 1.000 0.080 X 154863192 frameshift variant TT/- delins 0.700 0
dbSNP: rs387906462
rs387906462
F8
1 1.000 0.080 X 154896093 frameshift variant GA/- del 0.700 0
dbSNP: rs387906461
rs387906461
F8
1 1.000 0.080 X 154902117 frameshift variant C/- delins 0.700 0
dbSNP: rs387906460
rs387906460
F8
1 1.000 0.080 X 154903943 frameshift variant T/-;TT delins 0.700 0