81249 G6pd full gene sequence
Also known as: G6PD sequencing, G6PD full analysis
Complete sequence analysis of the G6PD gene to identify all point mutations and small indels causing G6PD deficiency.
In Plain Language
red blood cell enzyme test; comprehensive genetic testing
Clinical Context
Used for comprehensive G6PD screening in patients with hemolytic anemia to identify rare variants causing deficiency.
RVU Information
CPT 81249 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 81249?
CPT 81249 (G6pd full gene sequence) is a Pathology & Lab code. Complete sequence analysis of the G6PD gene to identify all point mutations and small indels causing G6PD deficiency.
Who uses CPT code 81249?
CPT 81249 is used by Genetics, Hematology, Pathology. Used for comprehensive G6PD screening in patients with hemolytic anemia to identify rare variants causing deficiency.
When is CPT 81249 used?
Used for comprehensive G6PD screening in patients with hemolytic anemia to identify rare variants causing deficiency.
Track This Code in RVU Edge
Log procedures, calculate wRVUs, and benchmark against national data — all in one app.
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.