DisGeNET - a database of gene-disease associations

IMPG2, interphotoreceptor matrix proteoglycan 2, 50939

N. diseases: 57; N. variants: 20

Disease: Retinal Dystrophies ×

Variant: rs878853358 ×

Source: ALL

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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:

rs878853358

rs878853358

Entrez Id:	50939
Gene Symbol:	IMPG2

IMPG2

CUI:	C0854723
Disease:

Retinal Dystrophies

G

0.700

GeneticVariation

CLINVAR