Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800386
rs1800386
VWF
0.710 GeneticVariation BEFREE We found the 4751A>G (Tyr1584Cys) sequence variation in exon 28, which is a common mutation in the Canadian VWD population (14.3%), in only one of the 31 families (3.2%). 16359504

2005
dbSNP: rs1800386
rs1800386
VWF
C 0.710 CausalMutation CLINVAR