81248 G6pd known familial variant
Also known as: G6PD familial variant testing, G6PD targeted analysis
Targeted mutation analysis of the G6PD gene to identify known familial variants causing G6PD deficiency.
In Plain Language
red blood cell enzyme test; family mutation detection
Clinical Context
Used to identify known G6PD mutations in family members of affected individuals for carrier status determination and genetic counseling.
RVU Information
CPT 81248 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 81248?
CPT 81248 (G6pd known familial variant) is a Pathology & Lab code. Targeted mutation analysis of the G6PD gene to identify known familial variants causing G6PD deficiency.
Who uses CPT code 81248?
CPT 81248 is used by Genetics, Hematology, Pathology. Used to identify known G6PD mutations in family members of affected individuals for carrier status determination and genetic counseling.
When is CPT 81248 used?
Used to identify known G6PD mutations in family members of affected individuals for carrier status determination and genetic counseling.
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.