{{Rsnum
|rsid=104894464
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=OTX2
|position=56802340
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTX2
}}{{omim
|id=600037
|rsnum=104894464
|variant=0002
}}{{ClinVar
|rsid=104894464
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=57269058
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=OTX2:5015
|GENE_NAME=OTX2
|GENE_ID=5015
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.57269058G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600037.0002
|CLNSIG=5
|CLNCUI=C1864690
|CLNDBN=Microphthalmia syndromic 5
|Disease=Microphthalmia syndromic 5
|CLNACC=RCV000010124.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864690:610125:178364
}}