Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63524161
rs63524161
VWF
0.020 GeneticVariation BEFREE C1272F: a novel type 2A von Willebrand's disease mutation in A1 domain; its clinical significance. 21592258

2012
dbSNP: rs63524161
rs63524161
VWF
0.020 GeneticVariation BEFREE C1272S: a new candidate mutation in type 2A von Willebrand disease that disrupts the disulfide loop responsible for the interaction of VWF with platelet GP Ib-IX. 14755371

2004