Cystic Fibrosis (CFTR) Panel
The CFTR gene and its best-known variants, including F508del, the most common cystic-fibrosis-causing variant.
1 gene · 3 variants
CF transmembrane conductance regulator
CFTR is a human protein-coding gene.
CFTR · p.Phe508del
rs113993960 is a genetic variant located in the CFTR gene.
CFTR · p.Ser549Asn
rs121908755 is a genetic variant located in the CFTR gene.
CFTR · p.Gly551Asp
rs75527207 is a genetic variant located in the CFTR gene.
Educational information only — not medical advice, a diagnosis, or a clinical recommendation. This panel is a curated grouping of public-record gene and variant pages for reference; it does not reflect your own genome or personal risk. Consult a qualified genetics professional or genetic counselor for interpretation relevant to you.