Cystic Fibrosis Screen

The Cystic Fibrosis Screen test contains 1 test with 7 biomarkers.

This test will identify approximately 90% of Cystic Fibrosis (CF) mutations in the Caucasian population, and 97% in the Ashkenazi Jewish population. For prenatal specimens, use test code 10226.

The following is a list of what is included in the item above. Click the test(s) below to view what biomarkers are measured along with an explanation of what the biomarker is measuring.

Also known as: CF Carrier Screen, CF Mutation Screen, CF Screen, CFTR Screen, Cystic Fibrosis Mutation Screen

CF RESULT

ETHNICITY:

INTERPRETATION

METHOD

MUTATIONS/POLYMORPHISMS

REPORTED ETHNICITY

REVIEWER

*Important Information on Lab Test Processing Times: Ulta Lab Tests is committed to informing you about the processing times for your lab tests processed through Quest Diagnostics. Please note that the estimated processing time for each test, indicated in business days, is based on data from the past 30 days across the 13 Quest Diagnostics laboratories for each test. These estimates are intended to serve as a guide and are not guarantees. Factors such as laboratory workload, weather conditions, holidays, and the need for additional testing or maintenance can influence actual processing times. We aim to offer estimates to help you plan accordingly. Please understand that these times may vary, and processing times are not guaranteed. Thank you for choosing Ulta Lab Tests for your laboratory needs.

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