VWF, von Willebrand factor, 7450

N. diseases: 498; N. variants: 158
Disease: von Willebrand Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61750071
rs61750071
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C0042974
Disease:
von Willebrand Disease 		A 0.710 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749 2019
dbSNP: rs61750071
rs61750071
Entrez Id: 7450
Gene Symbol: VWF
VWF
CUI: C0042974
Disease:
von Willebrand Disease 		0.710 GeneticVariation BEFREE von Willebrand disease R1374C: type 2A or 2M? A challenge to the revised classification. High frequency in the northwest of Spain (Galicia). 16247740 2005