DisGeNET - a database of gene-disease associations

Impaired cognition, C0338656

Variant: rs6439886 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs6439886

rs6439886

CLSTN2

0.010

GeneticVariation

BEFREE

No increased risk of any type of late development, and cognitive impairment was associated with rs6439886 or rs17070145.

2012