{{Rsnum
|rsid = 28940313
|Gene = RDH12
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=A
|MissenseAllele=G
|Chromosome=14
|position=67729209
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RDH12,ZFYVE26
}}{{omim
|desc=LEBER CONGENITAL AMAUROSIS, TYPE III
|id=608830
|rsnum=28940313
|variant=0001
}}{{ClinVar
|rsid=28940313
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=68195926
|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
|CLNHGVS=NC_000014.8:g.68195926A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608830.0001
|CLNSIG=5
|CLNCUI=C2675186
|CLNDBN=Leber congenital amaurosis 13
|Disease=Leber congenital amaurosis 13
|CLNACC=RCV000002127.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1298:NBK1417:C2675186:612712
}}

{{on chip | 23andMe v4}}