81240 F2 gene
Also known as: F2 gene testing, Prothrombin G20210A testing
Molecular analysis of the F2 gene to identify mutations associated with Prothrombin (Factor II) deficiency and thrombophilia.
In Plain Language
blood clotting gene test; thrombophilia genetic screening
Clinical Context
Used to detect Factor II G20210A variant associated with increased thrombosis risk for thrombophilia screening in patients with venous thromboembolism.
RVU Information
CPT 81240 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81240?
CPT 81240 (F2 gene) is a Pathology & Lab code. Molecular analysis of the F2 gene to identify mutations associated with Prothrombin (Factor II) deficiency and thrombophilia.
Who uses CPT code 81240?
CPT 81240 is used by Genetics, Hematology, Pathology. Used to detect Factor II G20210A variant associated with increased thrombosis risk for thrombophilia screening in patients with venous thromboembolism.
When is CPT 81240 used?
Used to detect Factor II G20210A variant associated with increased thrombosis risk for thrombophilia screening in patients with venous thromboembolism.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.