DisGeNET - a database of gene-disease associations

NOD2, nucleotide binding oligomerization domain containing 2, 64127

N. diseases: 3; N. variants: 20

Disease: Crohn Disease ×

Variant: rs2066845 ×

Source: GWASDB ×

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:

rs2066845

Entrez Id:	64127
Gene Symbol:	NOD2

NOD2

CUI:	C0010346
Disease:

Crohn Disease

1.000

GeneticVariation

GWASDB

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

18587394

2008

dbSNP:

rs2066845

Entrez Id:	64127
Gene Symbol:	NOD2

NOD2

CUI:	C0010346
Disease:

Crohn Disease

1.000

GeneticVariation

GWASDB

Systematic association mapping identifies NELL1 as a novel IBD disease gene.

17684544

2007

dbSNP:

rs2066845

Entrez Id:	64127
Gene Symbol:	NOD2

NOD2

CUI:	C0010346
Disease:

Crohn Disease

1.000

GeneticVariation

GWASDB

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

17804789

2007