Gene: SCNN1B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.410 Biomarker disease GENOMICS_ENGLAND Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis-like phenotypes. 23837941 2014
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.410 GeneticVariation disease LHGDN Could a defective epithelial sodium channel lead to bronchiectasis. 18507830 2008
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.410 Biomarker disease HPO