Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757740068
rs757740068
CRB1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		T 0.700 CausalMutation CLINVAR Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis. 21602930

2011