DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Vitiligo ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	64094
Gene Symbol:	SMOC2

SMOC2

CUI:	C0042900
Disease:	Vitiligo

Vitiligo

0.120

GeneticVariation

GWASDB

Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.

2010