Service Description

The Cystic Fibrosis 60 Mutation test screens for 60 common genetic mutations that cause cystic fibrosis (CF), a hereditary disorder affecting the lungs and digestive system. This test helps identify carriers and supports early diagnosis. Why it’s done: To identify carriers of cystic fibrosis mutations To assist in family planning or prenatal screening To support diagnosis in individuals with symptoms of CF To guide genetic counseling and personalized care Specimen Type: Blood draw or cheek swab Turnaround Time: Typically 7–14 business days Collection Available: In-office or mobile collection