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Cystic Fibrosis Complete Rare Variant Analysis, Entire Gene Sequence
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.
Cystic fibrosis (CF) is the most common recessive lethal genetic disorder affecting primarily Caucasians of Northern European descent, with an incidence of approximately 1 in 3300 births and a carrier rate of 1 in 29. This test analyzes approximately 1000 variants that account for reater than 98% of disease causing variants. This test is only appropriate when there is a strong likelihood of cystic fibrosis and the variant is not detected in the general cystic fibrosis variant panel and familial variants are unknown.
Next Generation Sequencing
See Laboratory Report
CF Complete™,CF Rare Mutation Analysis,CF Sequencing,CFTR Gene Sequencing,Cystic Fibrosis Entire Gene Sequencing,Cystic Fibrosis Rare Mutation Analysis,Cystic Fibrosis Sequencing,CF Entire Gene Sequencing
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.