DisGeNET - a database of gene-disease associations

HCG22, HLA complex group 22 (gene/pseudogene), 285834

N. diseases: 20; N. variants: 12

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:

rs9262615

Entrez Id:	285834
Gene Symbol:	HCG22

HCG22

CUI:	C0026769
Disease:

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9262635

Entrez Id:	285834
Gene Symbol:	HCG22

HCG22

CUI:	C0026769
Disease:

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9262636

Entrez Id:	285834
Gene Symbol:	HCG22

HCG22

CUI:	C0026769
Disease:

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007