DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Crohn Disease ×

Gene: IL23R ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1004819

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.860

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs2201841

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.850

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs10889677

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.850

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs1343151

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs11465804

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs10489629

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.700

GeneticVariation

GWASDB

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.

17068223

2006

dbSNP:

rs11209026

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.900

GeneticVariation

GWASDB

A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.

22936669

2013

dbSNP:

rs11209026

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.900

GeneticVariation

GWASDB

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.

22412388

2012

dbSNP:

rs11465804

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.

20570966

2010

dbSNP:

rs11209026

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.900

GeneticVariation

GWASDB

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

18587394

2008

dbSNP:

rs11805303

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.810

GeneticVariation

GWASDB

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

18587394

2008

dbSNP:

rs11465804

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

18587394

2008

dbSNP:

rs11209026

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.900

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs2201841

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.850

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs10889677

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.850

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs9988642

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs2902440

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs2064689

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs1343151

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs11465802

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs10889676

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.800

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs7539625

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.700

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs7518660

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.700

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs11804284

IL23R

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.700

GeneticVariation

GWASDB

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

17804789

2007

dbSNP:

rs11209008

IL23R ; C1orf141

CUI:	C0010346
Disease:	Crohn Disease

Crohn Disease

0.700

GeneticVariation

GWASDB

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

17804789

2007