rs137852228, F9

N. diseases: 2
Source: ALL
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
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
0.800 CausalMutation CLINVAR
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019