VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1063857
rs1063857
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE We confirmed the association between rs1063857 and CVD risk. 20940418 2011