• 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:
2 Diagnostic Centers found for PROTHROMBIN GENE MUTATION ANALYSIS in Surat
  • Shraddha Clinical Lab, 1/3821, First Floor, Desai Pole, Soni Faliya, Gopipura, Surat, Gujarat-395003

    0261 2599945, 0261 2599946, 9825052183

    Collection Center
  • Shop No.-U17, Ground Floor, Abhinandan Royale Complex, Opposite Rajhans Olympia, Bhatar Road, Surat, Gujarat-359001


    Collection Center