DisGeNET - a database of gene-disease associations

Source: GWASCAT

Disease: Hyperopia ×

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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:	348
Gene Symbol:	APOE

APOE

CUI:	C0020490
Disease:	Hyperopia

Hyperopia

0.100

GeneticVariation

GWASCAT

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.

30098192

2018

Entrez Id:	2894
Gene Symbol:	GRID1

GRID1

CUI:	C0020490
Disease:	Hyperopia

Hyperopia

0.100

GeneticVariation

GWASCAT

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.

30098192

2018

Entrez Id:	3908
Gene Symbol:	LAMA2

LAMA2

CUI:	C0020490
Disease:	Hyperopia

Hyperopia

0.100

GeneticVariation

GWASCAT

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.

25233373

2014

Entrez Id:	54715
Gene Symbol:	RBFOX1

RBFOX1

CUI:	C0020490
Disease:	Hyperopia

Hyperopia

0.100

GeneticVariation

GWASCAT

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.

25233373

2014