Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6337
Gene Symbol: SCNN1A
SCNN1A 		0.600 GeneticVariation disease UNIPROT Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease. 19462466 2009
Entrez Id: 6337
Gene Symbol: SCNN1A
SCNN1A 		0.600 Biomarker disease GENOMICS_ENGLAND Lung symptoms in pseudohypoaldosteronism type 1 are associated with deficiency of the alpha-subunit of the epithelial sodium channel. 10586178 1999
Entrez Id: 6337
Gene Symbol: SCNN1A
SCNN1A 		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