DisGeNET - a database of gene-disease associations

Vitiligo, C0042900

Variant: rs11964542 ×

Source: ALL

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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:

rs11964542

rs11964542

TRIM31 ; TRIM31-AS1

0.700

GeneticVariation

GWASDB

Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.

2010