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Test
test details

PROTHROMBIN (FACTOR II) MUTATION

MRP: ₹5200

Recommended For

maleMalefemaleFemale
  • Age Group
    Age Group0-99 Years
  • Report Generation Time
    Report Generation Time23-04-2024 08:22:44
  • Sample Type
    blood sampleEDTA Blood
  • Collection At
    home visitHomelab flaskLab
Description

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.

Pre-Information

Duly filled Genomics Clinical Information Requisition Form is mandatory.

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