Method of screening for the presence of the genetic defect associated with deep vein thrombosis

摘要

The present invention relates to a method indicates high risk of deep venous thrombosis, and screening individual genetic markers haplotype 2 of the fibrinogen γ gene shown in Figure 5A is a (FGG-H2) for the presence of the genome. It comprises a mutation of one to four of a set of nucleic acid material encoding the fibrinogen γ, wherein said mutation genetic marker 129A / T (rs2066854), 7874G / A (rs2066861), 9615C / T (rs2066864) and is selected from the group consisting of (rs2066865) 10034C / T.