Cystic Fibrosis Rare Variant Analysis, One Exon

Use

Cystic fibrosis (CF) is the most common recessive lethal genetic disorder, particularly affecting Caucasians of Northern European descent, with an incidence of approximately 1 in 3,300 births and a carrier rate of 1 in 29. Detection of a variant in one exon is useful in patients with a known familial variant that is not included in the general cystic fibrosis mutation panel. ([jdos.nicholsinstitute.com](https://jdos.nicholsinstitute.com/dos/questdemo/test/872397?utm_source=openai))