{{Rsnum
|rsid=121918165
|Chromosome=6
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LCA5
|position=79493636
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LCA5
}}{{omim
|id=611408
|rsnum=121918165
|variant=0003
}}{{ClinVar
|rsid=121918165
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=80203353
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000040002110100
|GENEINFO=LCA5:167691
|GENE_NAME=LCA5
|GENE_ID=167691
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.80203353G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1298; 611408.0003
|CLNSIG=5
|CLNCUI=C1858301
|CLNDBN=Leber congenital amaurosis 5
|Disease=Leber congenital amaurosis 5
|CLNACC=RCV000001019.2
|Tags=RV;PM;PMC;S3D;SLO;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1298:C1858301:604537:65
}}{{PMID Auto
|PMID=17546029
|Title=Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
}}