Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61749370
rs61749370
VWF
A 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs61749370
rs61749370
VWF
A 0.700 GeneticVariation CLINVAR Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients. 24675615

2014
dbSNP: rs61749370
rs61749370
VWF
A 0.700 GeneticVariation CLINVAR The genetic basis of von Willebrand disease. 20409624

2010
dbSNP: rs61749370
rs61749370
VWF
A 0.700 GeneticVariation CLINVAR Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients. 18805962

2009
dbSNP: rs61749370
rs61749370
VWF
A 0.700 GeneticVariation CLINVAR Genetic defects in von Willebrand disease type 3 in Indian and Greek patients. 18485763

2008
dbSNP: rs61749370
rs61749370
VWF
A 0.700 GeneticVariation CLINVAR von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure. 8486782

1993
dbSNP: rs61749370
rs61749370
VWF
T 0.700 CausalMutation CLINVAR