81247 G6pd gene alys cmn variant
Also known as: G6PD common variant panel, G6PD variant testing
Molecular analysis of the G6PD gene to identify common variants affecting glucose-6-phosphate dehydrogenase enzyme function.
In Plain Language
red blood cell enzyme test; hemolytic anemia genetic screening
Clinical Context
Used to identify G6PD deficiency variants in patients with hemolytic anemia triggered by infections, medications, or fava beans.
RVU Information
CPT 81247 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 81247?
CPT 81247 (G6pd gene alys cmn variant) is a Pathology & Lab code. Molecular analysis of the G6PD gene to identify common variants affecting glucose-6-phosphate dehydrogenase enzyme function.
Who uses CPT code 81247?
CPT 81247 is used by Genetics, Hematology, Pathology. Used to identify G6PD deficiency variants in patients with hemolytic anemia triggered by infections, medications, or fava beans.
When is CPT 81247 used?
Used to identify G6PD deficiency variants in patients with hemolytic anemia triggered by infections, medications, or fava beans.
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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.