DisGeNET - a database of gene-disease associations

Source: ALL

Disease: hearing impairment ×

Variant: rs1799883 ×

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:

rs1799883

rs1799883

FABP2

CUI:	C1384666
Disease:	hearing impairment

hearing impairment

0.010

GeneticVariation

BEFREE

This study demonstrated that the Ala54Thr polymorphism of FABP2 was associated with a risk of hearing impairment in middle-aged and elderly people.

2010