DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Crohn Disease ×

Gene: MIR3936HG ×

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:	553103
Gene Symbol:	MIR3936HG

MIR3936HG

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.100

GeneticVariation

GWASDB

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.

2007