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.
Parameter(s) covered : 1
Report Frequency: Sample Mon through Sat by 10 am; Report Next day
Special Instruction: Physician prescription is mandatory.
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Parameters
- Prothrombin gene Mutation