PROTHROMBIN GENE MUTATION ANALYSIS

  • Test Usage:
    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.
  • Report Availability:
    Sample by Mon / Thu 11 am; Report Wed / Sat
  • Sample Report:
23 Diagnostic Centers found for PROTHROMBIN GENE MUTATION ANALYSIS in Faridabad