rs137852267, F9

N. diseases: 1
Disease: Hemophilia B ×
Source: UNIPROT ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
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
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
0.800 GeneticVariation UNIPROT Clinical utility gene card for: haemophilia B. 22274582 2012