Cystic Fibrosis
Clinical genetic testing for cystic fibrosis looks for mutations in the gene causing the disease. This condition is most common in people of Caucasian and Ashkenazi (eastern and central European) Jewish ancestry, but can also occur in other ethnic groups.
This testing is for medical, clinical purposes.
This testing is available online at the Direct-to-Consumer Genetic Testing providers listed below.
Some providers also offer this testing as part of two larger panels: Ashkenazi Jewish Panel and Male Infertility Panel.
This testing is also available through many offline genetic testing providers if indicated by further evaluation and consultation with a trained genetic professional. Use the zip code search box to find a trained genetic professional in your area.
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Cystic Fibrosis - Selected Mutations (as part of Whole Genome Scan)
Cystic fibrosis testing by whole genome scanning looks for selected
mutations in the gene causing the disorder. Of note, this testing does not detect all known disease-causing mutations. Depending on the
methodology used, whole genome scanning is typically not as accurate
as conventional molecular genetic testing methods.
As such, individuals who are pregnant, have a personal or family history of the
disorder, or have a spouse who is a known carrier, may be better
candidates for conventional molecular testing methods. Test results
should be discussed with a genetic professional.
This testing is available online through the Direct-to-Consumer Genetic Testing providers listed below. A consultation with a trained genetic professional may be useful.
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