Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800385
rs1800385
VWF
0.010 GeneticVariation BEFREE ADAMTS13 haplotype had an independent protective effect on CAD and genetic variation of vWF V1565L polymorphism modulates ADAMTS13 activity. 27536857

2017

dbSNP: rs216311
rs216311
VWF
0.010 GeneticVariation BEFREE In summary, vWF gene polymorphisms at site A1381T were not associated with coronary heart disease, but plasma vWF levels were influenced by vWF gene polymorphisms at site A1381T, blood type and coronary heart disease. 22923007

2012

dbSNP: rs1063856
rs1063856
VWF
0.010 GeneticVariation BEFREE Impact of the Thr789Ala variant of the von Willebrand factor levels, on ristocetin co-factor and collagen binding capacity and its association with coronary heart disease in patients with diabetes mellitus type 2. 16320153

2005