Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs751205634
rs751205634
PRH1 ; PRH2 ; PRR4 ; PRH1-PRR4
0.010 GeneticVariation BEFREE The common von Willebrand disease type 2N mutation (R91Q) was excluded as a modifying factor in these groups of patients. 8695835

1996