DisGeNET - a database of gene-disease associations

Source: CTD_human

Disease: Pseudohypoaldosteronism, Type I ×

Gene: SCNN1A ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	6337
Gene Symbol:	SCNN1A

SCNN1A

CUI:	C0268436
Disease:	Pseudohypoaldosteronism, Type I

Pseudohypoaldosteronism, Type I

0.380

Biomarker

CTD_human

Association of a sodium channel alpha subunit promoter variant with blood pressure.

2002