DisGeNET - a database of gene-disease associations

RTEL1, regulator of telomere elongation helicase 1, 51750

N. diseases: 321; N. variants: 82

Disease: Crohn Disease ×

The Variant filter does not apply in GDA tabs

Source: ALL

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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.100

GeneticVariation

disease

GWASDB

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

2008