Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61750070
rs61750070
VWF
C 0.710 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs61750070
rs61750070
VWF
0.710 GeneticVariation BEFREE A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis. 18064311

2007
dbSNP: rs61750070
rs61750070
VWF
C 0.710 CausalMutation CLINVAR