81215 Brca1 gene known famil vrnt
Also known as: BRCA1 familial variant testing, BRCA1 targeted analysis
Targeted mutation analysis of the BRCA1 gene to identify known familial variants associated with hereditary breast and ovarian cancer.
In Plain Language
breast cancer gene test; family mutation detection
Clinical Context
Used to identify known BRCA1 pathogenic variants in family members of affected individuals for genetic counseling and cancer surveillance planning.
RVU Information
CPT 81215 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 81215?
CPT 81215 (Brca1 gene known famil vrnt) is a Pathology & Lab code. Targeted mutation analysis of the BRCA1 gene to identify known familial variants associated with hereditary breast and ovarian cancer.
Who uses CPT code 81215?
CPT 81215 is used by Oncology, Genetics, Pathology. Used to identify known BRCA1 pathogenic variants in family members of affected individuals for genetic counseling and cancer surveillance planning.
When is CPT 81215 used?
Used to identify known BRCA1 pathogenic variants in family members of affected individuals for genetic counseling and cancer surveillance planning.
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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.