81269 Hba1/hba2 gene dup/del vrnts
Also known as: Alpha globin copy number analysis, HBA duplication deletion
Hemoglobin Alpha 1 and Alpha 2 genes duplication and deletion variant analysis to identify gene copy number variations associated with alpha thalassemia.
In Plain Language
Alpha thalassemia trait testing; Red blood cell gene deletion test
Clinical Context
Detects common deletions and duplications causing alpha thalassemia trait and disease. Critical for carrier screening and determination of disease severity.
RVU Information
CPT 81269 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 81269?
CPT 81269 (Hba1/hba2 gene dup/del vrnts) is a Pathology & Lab code. Hemoglobin Alpha 1 and Alpha 2 genes duplication and deletion variant analysis to identify gene copy number variations associated with alpha thalassemia.
Who uses CPT code 81269?
CPT 81269 is used by Pathology, Hematology, Genetics. Detects common deletions and duplications causing alpha thalassemia trait and disease. Critical for carrier screening and determination of disease severity.
When is CPT 81269 used?
Detects common deletions and duplications causing alpha thalassemia trait and disease. Critical for carrier screening and determination of disease severity.
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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.