QA1.791: Familial cancer syndrome with pathogenic BRCA2 mutation
Familial cancer syndrome with pathogenic BRCA2 mutation
Quick Clinical & Billing Summary
What is ICD-10-CM code QA1.791? QA1.791 represents Familial cancer syndrome with pathogenic BRCA2 mutation. Under official CDC guidelines, this code is billable and specific for claim submission.
Code Hierarchy & Classification
Clinical Guidance & Documentation Standards
Associated Procedures & Medicare RVU Reimbursement
Open RVU Calculator →Typical outpatient and office evaluation procedures frequently billed alongside diagnosis QA1.791:
| CPT/HCPCS | Description | Work RVU | Non-Facility Fee | Facility Fee |
|---|---|---|---|---|
| 99213 | Office/outpatient visit, established patient, 20-29 minutes (Low MDM) | 1.30 | $91.69 | $66.79 |
| 99214 | Office/outpatient visit, established patient, 30-39 minutes (Moderate MDM) | 1.92 | $133.61 | $100.21 |
| 96372 | Therapeutic, prophylactic, or diagnostic injection (subcutaneous/intramuscular) | 0.17 | $18.34 | $12.44 |
CPT Modifier & Billing Rules
Append when a significant, separately identifiable evaluation and management service is provided on the same calendar day as a minor surgical procedure or injection.
Identifies procedures or services not normally reported together but distinct under the clinical circumstances. Use CMS X-modifiers (XE, XS, XP, XU) where required by Medicare.
Frequently Asked Questions about QA1.791
Is QA1.791 a billable ICD-10 code?
Yes, QA1.791 is a valid, billable and specific ICD-10-CM code. It can be reported as a primary or secondary diagnosis on medical claims.
What is the ICD-10 code for Familial cancer syndrome with pathogenic BRCA2 mutation?
The primary ICD-10-CM code for Familial cancer syndrome with pathogenic BRCA2 mutation is QA1.791.
What is the effective date of the current QA1.791 code?
The code is active for fiscal year FY2027, effective starting 2026-10-01.
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