Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61751286
rs61751286
VWF
A 0.700 CausalMutation CLINVAR Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study. 19566550

2009
dbSNP: rs61751286
rs61751286
VWF
A 0.700 CausalMutation CLINVAR 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). 16985174

2007
dbSNP: rs61751286
rs61751286
VWF
A 0.700 CausalMutation CLINVAR The mutational spectrum of type 1 von Willebrand disease: Results from a Canadian cohort study. 17190853

2007