DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Hypertensive disease ×

Gene: NR3C1 ×

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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:	2908
Gene Symbol:	NR3C1

NR3C1

CUI:	C0020538
Disease:	Hypertensive disease

Hypertensive disease

0.700

GeneticVariation

LHGDN

A novel point mutation in the amino terminal domain of the human glucocorticoid receptor (hGR) gene enhancing hGR-mediated gene expression.

2008