81220 Cftr gene com variants
Also known as: CFTR common variant panel, Cystic Fibrosis common mutation testing
Molecular analysis of the CFTR gene to identify common pathogenic variants associated with Cystic Fibrosis.
In Plain Language
cystic fibrosis gene test; lung disease genetic screening
Clinical Context
Used as a screening test for Cystic Fibrosis in newborns and carrier screening in at-risk populations.
RVU Information
CPT 81220 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 81220?
CPT 81220 (Cftr gene com variants) is a Pathology & Lab code. Molecular analysis of the CFTR gene to identify common pathogenic variants associated with Cystic Fibrosis.
Who uses CPT code 81220?
CPT 81220 is used by Genetics, Pulmonology, Pathology. Used as a screening test for Cystic Fibrosis in newborns and carrier screening in at-risk populations.
When is CPT 81220 used?
Used as a screening test for Cystic Fibrosis in newborns and carrier screening in at-risk populations.
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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.