Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863223342
rs863223342
CRB1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		CT 0.700 CausalMutation CLINVAR Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 26497376

2015