Disease: Retinal Dystrophies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768660614
rs768660614
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease:
Retinal Dystrophies 		GT 0.700 GeneticVariation CLINVAR