{{Rsnum
|rsid=137852833
|Chromosome=12
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CEP290
|position=88111320
|Gene_s=CEP290
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=610142
|variant=0006
|rsnum=137852833
}}{{ClinVar
|rsid=137852833
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=88505097
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CEP290:80184
|GENE_NAME=CEP290
|GENE_ID=80184
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.88505097A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610142.0006
|CLNSIG=5
|CLNCUI=C1857821
|CLNDBN=Leber congenital amaurosis 10
|Disease=Leber congenital amaurosis 10
|CLNACC=RCV000001401.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1298:NBK1325:C1857821:611755:65
}}