Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61749398
rs61749398
VWF
0.710 GeneticVariation BEFREE In contrast, the antibodies failed to detect conformational change in the G1324S mutant (type 2M von Willebrand disease). 16420575

2006
dbSNP: rs61749398
rs61749398
VWF
T 0.710 CausalMutation CLINVAR