{{Rsnum
|rsid=104894492
|Chromosome=15
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NR2E3
|position=71811590
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NR2E3
}}{{omim
|id=604485
|rsnum=104894492
|variant=0002
}}{{ClinVar
|rsid=104894492
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=72103930
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NR2E3:10002
|GENE_NAME=NR2E3
|GENE_ID=10002
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.72103930C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604485.0002
|CLNSIG=5
|CLNCUI=C1849394
|CLNDBN=Enhanced s-cone syndrome
|Disease=Enhanced s-cone syndrome
|CLNACC=RCV000005866.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849394:268100:53540
}}