Variant: rs137852228

present in Gene: F9 present in Chromosome: X Position on Chromosome: 139537145 Alleles of this Variant: G/A

rs137852228 in F9 gene and Hemophilia A PMID 31064749 2019 Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.

rs137852228 in F9 gene and Hemophilia B PMID 23157203 2013 Diagnosis and treatment of factor VIII and IX inhibitors in congenital haemophilia: (4th edition). UK Haemophilia Centre Doctors Organization.

PMID 22274582 2012 Clinical utility gene card for: haemophilia B.