VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
Disease: Endothelial dysfunction ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1395198370
rs1395198370
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C0856169
Disease:
Endothelial dysfunction 		0.010 GeneticVariation BEFREE The aim of this study was to search for an association between V249I and T280M polymorphisms of CX3CR1, preeclampsia and endothelial dysfunction. 19587779 2009