Disease: Retinal Dystrophies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs758291149
rs758291149
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease:
Retinal Dystrophies 		T 0.700 CausalMutation CLINVAR Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. 20673862 2010
dbSNP: rs768660614
rs768660614
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease:
Retinal Dystrophies 		GT 0.700 GeneticVariation CLINVAR
dbSNP: rs878853357
rs878853357
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease:
Retinal Dystrophies 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs878853358
rs878853358
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease:
Retinal Dystrophies 		G 0.700 GeneticVariation CLINVAR