{{Rsnum
|rsid=62635659
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CRB1
|position=197435162
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CRB1
}}{{omim
|id=604210
|rsnum=62635659
|variant=0006
}}{{ClinVar
|rsid=62635659
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=197435162
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360080a05000002110100
|GENEINFO=CRB1:23418
|GENE_NAME=CRB1
|GENE_ID=23418
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.197435162T>C; NC_000001.11:g.197435162T>G
|CLNSRC=ClinVar; Retina International; OMIM Allelic Variant
|CLNORIGIN=0; 1
|CLNSRCID=NM_001257966.1:c.2129-438T>C; NM_201253.2:c.3299T>C; NR_047563.1:n.3300T>C; RISN-CRB1:c.3299T>C; NM_001257966.1:c.2129-438T>G; NM_201253.2:c.3299T>G; NR_047563.1:n.3300T>G; 604210.0006; RISN-CRB1:c.3299T>G
|CLNSIG=5
|CLNCUI=C3151202
|CLNDBN=not provided; Leber congenital amaurosis 8
|Disease=not provided; Leber congenital amaurosis 8
|CLNACC=RCV000086339.1; RCV000006088.1; RCV000086340.1
|Tags=PM;S3D;SLO;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1298:C3151202:613835:ORPHA65
}}