DisGeNET - a database of gene-disease associations

Crohn Disease, C0010346

Source: ALL

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs104895467

NOD2

0.720

GeneticVariation

UNIPROT

dbSNP:

rs104895483

NOD2

0.710

GeneticVariation

UNIPROT

dbSNP:

rs3813758

NOD2

0.710

GeneticVariation

UNIPROT

dbSNP:

rs62029861

NOD2

0.710

GeneticVariation

UNIPROT

dbSNP:

rs104895428

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895429

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895431

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895432

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895438

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895439

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895440

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895442

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895443

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895444

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895445

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895446

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895447

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895453

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895468

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895469

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895470

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs104895471

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs34684955

NOD2

0.700

GeneticVariation

UNIPROT

dbSNP:

rs1217691063

MTHFR

0.040

GeneticVariation

BEFREE

A total of 17.5% of ulcerative colitis and 16.8% of Crohn's disease patients were homozygous for the C677T variant compared with 7.3% of controls.

10446107

1999

dbSNP:

rs145922845

IL10 ; IL19

0.030

GeneticVariation

BEFREE

Screening of the coding region of the IL-10 gene by polymerase chain reaction--single strand conformation polymorphism (PCR-SSCP) analysis revealed a rare sequence variation in exon 1 leading to an amino acid exchange (G-->A; G15R) in two patients with CD and five healthy controls.

11271474

2000