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Test Name

CFvantage® Cystic Fibrosis Expanded Screen

To view specimen requirements and codes please Select a regional laboratory.

Not sure which laboratory serves your office? Call us 866-MYQUEST (866-697-8378)

CPT Code(s)**

81220
**IMPORTANT: CPT Code is informational only; obtain the Test Code for ordering.

Physician Attestation of Informed Consent

This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA.

Clinical Significance

The CFvantage® Cystic Fibrosis Expanded Screen analyzes an expanded number of variants that have been proven to cause Cystic Fibrosis (CF). This panel includes the 23 variants recommended by the American College of Obstetricians and Gynecologists (ACOG) for screening of all women of childbearing age. ACOG also recommends that patients with a personal or family history of CF be offered screening.

Methodology

Multiplex PCR • Next Generation Sequencing

Reference Range(s)

See Laboratory Report

Test FAQ

CFvantage Cystic Fibrosis Expanded Screen

Alternative Name(s)

CF Mutation Screen,CFTR Expanded Mutation Screen,CF155 Mutations,Cystic Fibrosis Mutation Screen,CFTR Screen,CF Carrier Screen,CF Expanded Mutation Carrier Screen,Cystic Fibrosis Expanded Panel,Cystic Fibrosis Carrier Screen

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.

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CFvantage® Cystic Fibrosis Expanded Screen
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