Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1246069621
rs1246069621
VWF
0.010 GeneticVariation BEFREE In conclusion, a haplotype containing the <i>STXBP5</i> Asn436Ser (rs1039084) mutation is associated with type 1 VWD and no rare <i>STXBP5</i> mutations contribute to type 1 VWD in the Swedish population. 29972863

2018