DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Multiple Sclerosis ×

Gene: HLA-DQA2 ×

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:

rs2227127

HLA-DQA2

CUI:	C0026769
Disease:	Multiple Sclerosis

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9276429

HLA-DQA2

CUI:	C0026769
Disease:	Multiple Sclerosis

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9276431

HLA-DQA2

CUI:	C0026769
Disease:	Multiple Sclerosis

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9276432

HLA-DQA2

CUI:	C0026769
Disease:	Multiple Sclerosis

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007

dbSNP:

rs9276440

HLA-DQA2

CUI:	C0026769
Disease:	Multiple Sclerosis

Multiple Sclerosis

0.700

GeneticVariation

GWASDB

Risk alleles for multiple sclerosis identified by a genomewide study.

17660530

2007