Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553263218
rs1553263218
CRB1
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		TG 0.700 CausalMutation CLINVAR An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy. 18055820

2007