rs41276738, VWF

N. diseases: 7
Disease: von Willebrand Disease, Type 2 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
von Willebrand Disease, Type 2
CUI: C1264040
Disease: von Willebrand Disease, Type 2
0.810 GeneticVariation BEFREE The cause of this was subsequently shown to be the Normandy variant of type-2 von Willebrand's disease due to a homozygous Arg854Gln mutation in the von Willebrand factor gene. 15113383 2004
von Willebrand Disease, Type 2
CUI: C1264040
Disease: von Willebrand Disease, Type 2
0.810 CausalMutation CLINVAR
von Willebrand Disease, Type 2
CUI: C1264040
Disease: von Willebrand Disease, Type 2
0.810 GeneticVariation UNIPROT