DisGeNET - a database of gene-disease associations

Source: BEFREE

Disease: Severe myopia ×

Gene: ZNF469 ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	84627
Gene Symbol:	ZNF469

ZNF469

CUI:	C0271183
Disease:	Severe myopia

Severe myopia

0.110

GeneticVariation

BEFREE

The average number of ZNF469 non-synonymous variants was 16.31 and 16.0 for individuals with KTCN and HM, respectively (p = 0.3724).

2016