Gene: F8 ×
Source: UNIPROT ×
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: rs28933676
rs28933676
F8
1 1.000 0.080 X 154904864 missense variant T/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852384
rs137852384
F8
1 1.000 0.080 X 154997038 missense variant T/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852388
rs137852388
F8
1 1.000 0.080 X 154993141 missense variant T/G snv 1.8E-04 1.8E-04 0.800 1.000 2 2011 2013
dbSNP: rs137852395
rs137852395
F8
1 1.000 0.080 X 154992983 missense variant T/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852427
rs137852427
F8
1 1.000 0.080 X 154953981 missense variant T/C;G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852406
rs137852406
F8
1 0.925 0.080 X 154969400 missense variant T/C snv 5.5E-06 0.810 1.000 22 1989 2014
dbSNP: rs137852420
rs137852420
F8
1 1.000 0.080 X 154957027 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852429
rs137852429
F8
1 1.000 0.080 X 154953903 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852454
rs137852454
F8
1 1.000 0.080 X 154902053 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852459
rs137852459
F8
1 0.925 0.080 X 154896135 missense variant T/C snv 5.5E-06 0.800 1.000 22 1989 2013
dbSNP: rs137852470
rs137852470
F8
1 1.000 0.080 X 154860538 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852476
rs137852476
F8
1 1.000 0.080 X 155022449 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933671
rs28933671
F8
1 1.000 0.080 X 154966471 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933679
rs28933679
F8
1 1.000 0.080 X 154904511 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933682
rs28933682
F8
1 1.000 0.080 X 154904082 missense variant T/C snv 0.800 1.000 22 1989 2013
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: rs1312347909
rs1312347909
F8
1 1.000 0.080 X 154997059 missense variant T/C snv 0.700 1.000 20 1989 2002
dbSNP: rs1354815715
rs1354815715
F8
1 1.000 0.080 X 154956958 missense variant T/C snv 0.700 1.000 20 1989 2002
dbSNP: rs137852412
rs137852412
F8
1 0.925 0.080 X 154961137 missense variant T/C snv 0.700 1.000 20 1989 2002
dbSNP: rs137852419
rs137852419
F8
1 1.000 0.080 X 154957049 missense variant T/C snv 5.5E-06 0.800 1.000 20 1989 2002
dbSNP: rs1441830456
rs1441830456
F8
1 1.000 0.080 X 154966088 missense variant T/C snv 0.700 1.000 20 1989 2002
dbSNP: rs1460318222
rs1460318222
F8
1 1.000 0.080 X 154953994 missense variant T/C snv 0.700 1.000 20 1989 2002
dbSNP: rs137852359
rs137852359
F8
1 1.000 0.080 X 154969468 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852362
rs137852362
F8
1 1.000 0.080 X 154928607 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852369
rs137852369
F8
1 1.000 0.080 X 154904083 missense variant T/C snv 0.800 1.000 2 2011 2013