Gene: F8 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111033615
rs111033615
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852403
rs137852403
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852403
rs137852403
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002
dbSNP: rs137852403
rs137852403
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852403
rs137852403
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852406
rs137852406
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852406
rs137852406
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002
dbSNP: rs137852406
rs137852406
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852406
rs137852406
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852410
rs137852410
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002
dbSNP: rs137852410
rs137852410
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852410
rs137852410
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852410
rs137852410
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852428
rs137852428
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002
dbSNP: rs137852428
rs137852428
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852428
rs137852428
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852428
rs137852428
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852431
rs137852431
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852431
rs137852431
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852431
rs137852431
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002
dbSNP: rs137852431
rs137852431
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852442
rs137852442
F8
0.810 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002
dbSNP: rs137852442
rs137852442
F8
0.810 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002
dbSNP: rs137852442
rs137852442
F8
0.810 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002
dbSNP: rs137852442
rs137852442
F8
0.810 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002