DisGeNET - a database of gene-disease associations

MOBP, myelin associated oligodendrocyte basic protein, 4336

N. diseases: 20; N. variants: 7

Disease: Alzheimer's Disease ×

Variant: rs538867 ×

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:

rs538867

Entrez Id:	4336
Gene Symbol:	MOBP

MOBP

CUI:	C0002395
Disease:

Alzheimer's Disease

0.800

GeneticVariation

GWASDB

Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.

23535033

2014