My Recent Searches
- No Recent Search.
My Tests Viewed
- No Test Viewed.
Cystic Fibrosis Rare Mutation Analysis, Two Exon
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)
**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.
This test is offered to individuals to: 1) detect a known familial CF mutation which is not examined in population-based CF carrier screening assay in at-risk individuals; 2) provide prenatal detection of a known familial CF mutation which is not examined in the general CF screening assay.
Dye-Terminator Sequencing Reaction • Polymerase Chain Reaction (PCR)
See Laboratory Report
Cystic Fibrosis Analysis,CF, Two Exon
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.