Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800383
rs1800383
VWF
0.020 GeneticVariation BEFREE Of these 23 patients, 6 with borderline low VWF:RCo were given provisional diagnosis of VWD type 1 by treating physicians, which could be alternatively explained as due to the effect of p.D1472H. 24581275

2014

dbSNP: rs1800383
rs1800383
VWF
0.020 GeneticVariation BEFREE These results suggest that the presence of the D1472H sequence variation is not associated with a significant increase in bleeding symptoms, even in type 1 VWD subjects. 23520336

2013