Our test studied 5 single nucleotide polymorphisms (SNP) with the highest individual odds ratio for venous thrombosis (25) (Factor V Leiden, PT G20210A, A1 blood group, 1 SNP in the Fibrinogen -gene, 1 in the Factor XI gene) as well as some rare genetic variants linked to the thrombosis risk, with stronger effects in the carriers, such as the SERPIN C1 gene (26), the R67X in SERPIN A10 gene (27), or Ser219Gly in the PROCR gene (28). The gene discussed is PROCR; the disease is deep vein thrombosis.