OUTSOURCE
Prothrombin Gene mutation ananlysis (N048)
Also Known As:
PT Gene Mutation
Factor II by PCR
Factor 2 Mutation (G20210A) by PCR
Prothrombin Mutation G20210A by PCR
About This Test
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.
Test Parameters (1)
- Prothrombin Gene mutation ananlysis
Home Collection
✓ Available
Reports Available In
3 Days
Frequently Asked Questions
Outsourced test are being done from Dr. Lal Path Lab. Charges and reporting time is same as of Dr. Lal Path Labs.
Physician prescription is mandatory.
The PT Gene Mutation Test (Prothrombin Gene Mutation – G20210A) is important because it helps identify an inherited risk of abnormal blood clot formation, allowing early prevention and targeted management of thrombotic complications.
TAT Policy
The Turnaround Time (TAT) depends on the following factors:
- Registration date and time
- Type of scan or test
- Scan time or sample collection time
In uncommon circumstances, TAT may be delayed due to test complexity or reasons beyond our control. You will be informed of the estimated TAT at the time of registration.
