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:

rs76418789

IL23R ; C1orf141

0.850

GeneticVariation

BEFREE

<b>Results:</b> Two <i>IL23R</i> SNPs, rs76418789 (G149R), and rs1495965, were associated with CD in Korean pediatric patients as defense and risk loci, respectively.

31799225

2019

dbSNP:

rs2066844

NOD2

1.000

GeneticVariation

BEFREE

507 unrelated CD patients were genotyped for the three major CD-associated variants (Arg702Trp, Gly908Arg, and Leu1007fsinsC) and for thirteen HLA-DRB1 alleles.

15046222

2004