VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
Disease: Cardiovascular Diseases ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs216293
rs216293
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.010 GeneticVariation BEFREE For ht-SNP rs4764478 (intron 45), the increase in VWF:Ag levels and VWF:CB activity per minor allele was 0.082 (± 0.026) IU/mL (P = .001) and 0.096 (± 0.030) IU/mL (P = .002), respectively. ht-SNP rs216293 (intron 17) was associated with CVD risk (odds ratio, 1.44; 95% confidence interval [CI], 1.12-1.86 per minor allele). 20940418 2011