DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Retinal Vein Occlusion ×

Variant: rs662 ×

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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:

rs662

PON1

CUI:	C0035328
Disease:	Retinal Vein Occlusion

Retinal Vein Occlusion

0.010

GeneticVariation

BEFREE

To determine if the paraoxonase 1 L55M and paraoxonase 1 Q192R gene polymorphisms have an effect on the risk of having a retinal vein occlusion (RVO).

23441121

2013