F8, coagulation factor VIII, 2157

N. diseases: 149; N. variants: 275
Disease: Hemophilia A ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852373
rs137852373
Entrez Id: 2157
Gene Symbol: F8
F8
CUI: C0019069
Disease:
Hemophilia A 		0.800 GeneticVariation UNIPROT Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition). UK Haemophilia Centre Doctors Organization. 23157203 2013
dbSNP: rs137852373
rs137852373
Entrez Id: 2157
Gene Symbol: F8
F8
CUI: C0019069
Disease:
Hemophilia A 		0.800 GeneticVariation UNIPROT Clinical utility gene card for: haemophilia A. 21654722 2011
dbSNP: rs137852373
rs137852373
Entrez Id: 2157
Gene Symbol: F8
F8
CUI: C0019069
Disease:
Hemophilia A 		T 0.800 CausalMutation CLINVAR