{{Rsnum
|rsid=104894672
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CRX
|position=47836263
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CRX
}}{{omim
|id=602225
|rsnum=104894672
|variant=0005
}}{{ClinVar
|rsid=104894672
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=48339520
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=CRX:1406
|GENE_NAME=CRX
|GENE_ID=1406
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.48339520C>T
|CLNSRC=OMIM Allelic Variant; Retina International
|CLNORIGIN=1
|CLNSRCID=602225.0005; RISN-CRX:c.121C>T
|CLNSIG=5
|CLNCUI=CN074280
|CLNDBN=Cone-rod dystrophy 2; not provided
|Disease=Cone-rod dystrophy 2; not provided
|CLNACC=RCV000007843.1; RCV000085989.1
|Tags=PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074280:120970:1872
}}