105 additional genetic markers that cause CF pinpointed



This web site, a product of The Cystic Fibrosis Foundation, Johns Hophins Medicine, and Sequenom contains a wealth of information that should provide
answers to your questions.


As it states:

Welcome to the Clinical and Functional Translation of CFTR (CFTR2) website
CFTR2 is a website designed to provide information about specific cystic fibrosis (CF) mutations to patients, researchers, and the general public. For each mutation included in the database, the website will provide information about:

  • Whether the mutation causes cystic fibrosis when combined with another CF-causing mutation, and
  • Information about the sweat chloride, lung function, pancreatic status, and pseudomonas infection rates in patients in the CFTR2 database with this mutation