DisGeNET - a database of gene-disease associations

SLC22A23, solute carrier family 22 member 23, 63027

N. diseases: 18; N. variants: 14

Disease: Crohn Disease ×

Variant: rs17309827 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs17309827

Entrez Id:	63027
Gene Symbol:	SLC22A23

SLC22A23

CUI:	C0010346
Disease:

Crohn Disease

0.800

GeneticVariation

GWASDB

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.

21102463

2010

dbSNP:

rs17309827

Entrez Id:	63027
Gene Symbol:	SLC22A23

SLC22A23

CUI:	C0010346
Disease:

Crohn Disease

0.800

GeneticVariation

GWASCAT

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.

21102463

2010

dbSNP:

rs17309827

Entrez Id:	63027
Gene Symbol:	SLC22A23

SLC22A23

CUI:	C0010346
Disease:

Crohn Disease

0.800

GeneticVariation

GWASDB

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

18587394

2008