Source: CTD_human

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6337
Gene Symbol: SCNN1A
SCNN1A
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Dominant 		0.300 Biomarker CTD_human Association of a sodium channel alpha subunit promoter variant with blood pressure. 11752024

2002