{{Rsnum
|rsid=61752895
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RPE65
|position=68439586
|Gene_s=RPE65
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61752895
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=68439586
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000605000002110100
|GENEINFO=RPE65:6121
|GENE_NAME=RPE65
|GENE_ID=6121
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.68439586G>A
|CLNSRC=ClinVar; OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=NM_000329.2:c.700C>T; 180069.0002; RISN-RPE65:c.700C>T
|CLNSIG=5
|CLNCUI=C1859844
|CLNDBN=Leber congenital amaurosis 2; not provided
|Disease=Leber congenital amaurosis 2; not provided
|CLNACC=RCV000013993.16; RCV000085219.1
|Tags=RV;PM;S3D;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1298:C1859844:204100:ORPHA65
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}