Annexin A2 SNP and von Willebrand Disease.

摘要

The present disclosure relates to an in vitro method for determining Von Willebrand Disease or an increased risk of developing Von Willebrand Disease. The method involves determining whether a point mutation at a defined position is present or absent in the ANXA2 gene sequence. Also disclosed is a kit for determining Von Willebrand Disease or an increased risk of developing Von Willebrand Disease comprising means for determining the point mutation.