PROTHROMBIN GENE MUTATION ANALYSIS

The prothrombin G20210A mutation is the second most common inherited predisposition to hypercoagulability. Heterozygous prothrombin G20210A mutation is associated with a 2 to 6 fold increased lifetime relative risk of VTE. This risk is further increased in combination with pregnancy and OCP use.

  • Test Type:
  • Pre-test Information:
    No special preparation required
  • Report Delivery:
    Sample by Mon / Thu 11 am; Report Wed / Sat
  • Components:
    0

Sample Report

prothrombin gene mutation analysis in other Cities