{{Rsnum
|rsid=104894475
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=RDH12
|position=67726983
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=LOC102723898,RDH12
}}{{omim
|id=608830
|rsnum=104894475
|variant=0007
}}
{{omim
|id=608830
|rsnum=104894475
|variant=0009
}}{{ClinVar
|rsid=104894475
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=68193700
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RDH12:145226
|GENE_NAME=RDH12
|GENE_ID=145226
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000014.8:g.68193700C>A; NC_000014.8:g.68193700C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608830.0007; 608830.0009
|CLNSIG=5
|CLNCUI=C2675186
|CLNDBN=Leber congenital amaurosis 13
|Disease=Leber congenital amaurosis 13
|CLNACC=RCV000002133.1; RCV000002135.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1298:NBK1417:C2675186:612712
}}