Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B
0.300 GermlineCausalMutation disease ORPHANET Recommendations for the classification of diseases as CFTR-related disorders. 21658649 2011
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B
0.300 GermlineCausalMutation disease ORPHANET Could a defective epithelial sodium channel lead to bronchiectasis. 18507830 2008