Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.600 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 		0.600 GeneticVariation disease UNIPROT Genetic analysis of Rwandan patients with cystic fibrosis-like symptoms: identification of novel cystic fibrosis transmembrane conductance regulator and epithelial sodium channel gene variants. 19017867 2009
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.600 GeneticVariation disease UNIPROT Could a defective epithelial sodium channel lead to bronchiectasis. 18507830 2008
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.600 GeneticVariation disease UNIPROT Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. 16207733 2005
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.600 Biomarker disease GENOMICS_ENGLAND Liddle's syndrome caused by a novel mutation in the proline-rich PY motif of the epithelial sodium channel beta-subunit. 15483078 2005
Entrez Id: 6338
Gene Symbol: SCNN1B
SCNN1B 		0.600 Biomarker disease CTD_human
Entrez Id: 1080
Gene Symbol: CFTR
CFTR 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 1080
Gene Symbol: CFTR
CFTR 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 1080
Gene Symbol: CFTR
CFTR 		0.600 CausalMutation disease CLINVAR
Entrez Id: 1080
Gene Symbol: CFTR
CFTR 		0.600 Biomarker disease CTD_human
Entrez Id: 771
Gene Symbol: CA12
CA12 		0.010 GeneticVariation disease BEFREE Mutation in the CAXII gene causes cystic fibrosis-like syndrome and salt wasting disease. 28433659 2017