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:
2 Diagnostic Centers found for PROTHROMBIN GENE MUTATION ANALYSIS in Rajkot
  • B/4,Pushkandham,University Road,Rajkot, Guajrat-360005


    9409018786

    Collection Center
  • Matrukrupa 1, Shakti Colony, Behind A.G. Office, Kishan Para Chowk, Rajkot, Gujarat-360001


    7878408665

    latiadiagnostics@gtmail.comq

    Collection Center