Variant: rs1555198839 

    present in Gene: VWF
    present in Chromosome: 12
    Position on Chromosome: 6062953
    Alleles of this Variant: C/A

rs1555198839 in VWF gene and Multiple congenital anomalies PMID 16634745 2006 A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD).

PMID 26288715 2015 Current controversies in the diagnosis and management of von Willebrand disease.

PMID 16862529 2006 Genetic testing for von Willebrand disease: the Canadian experience.

PMID 3495304 1987 The effect of ABO blood group on the diagnosis of von Willebrand disease.

PMID 2563148 1989 Birth of the D-E-A-D box.

PMID 22197721 2012 VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.

PMID 16985174 2007 Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).

PMID 23401897 1999 Diagnosis and management of von Willebrand disease.

PMID 16889557 2006 Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.

PMID 19372260 2009 A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3.

PMID 24319188 2013 von Willebrand disease: advances in pathogenetic understanding, diagnosis, and therapy.

PMID 11686102 2001 Congenital von Willebrand disease type I: definition, phenotypes, clinical and laboratory assessment.

PMID 17190853 2007 The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study.