81222 Cftr gene dup/delet variants
Also known as: CFTR dup/del testing, CFTR structural variant analysis
Duplication and deletion analysis of the CFTR gene to identify structural variants associated with Cystic Fibrosis.
In Plain Language
cystic fibrosis gene test; CFTR deletion detection
Clinical Context
Used to identify CFTR deletions and duplications in Cystic Fibrosis families for comprehensive genetic assessment.
RVU Information
CPT 81222 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 81222?
CPT 81222 (Cftr gene dup/delet variants) is a Pathology & Lab code. Duplication and deletion analysis of the CFTR gene to identify structural variants associated with Cystic Fibrosis.
Who uses CPT code 81222?
CPT 81222 is used by Genetics, Pulmonology, Pathology. Used to identify CFTR deletions and duplications in Cystic Fibrosis families for comprehensive genetic assessment.
When is CPT 81222 used?
Used to identify CFTR deletions and duplications in Cystic Fibrosis families for comprehensive genetic assessment.
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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.