Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607326
rs267607326
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C1264040
Disease:
von Willebrand Disease, Type 2
C 0.700 CausalMutation CLINVAR