Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61749392
rs61749392
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1282971
Disease:
von Willebrand Disease, Type 2B
G 0.700 CausalMutation CLINVAR