Variant: rs137852709 

    present in Gene: SCNN1B
    present in Chromosome: 16
    Position on Chromosome: 23367879
    Alleles of this Variant: C/T

rs137852709 in SCNN1B gene and BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1 PMID 19017867 2009 Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants.

PMID 18507830 2008 Could a defective epithelial sodium channel lead to bronchiectasis.

PMID 16207733 2005 Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome.