{{Rsnum
|rsid=104894493
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NR2E3
|position=71811591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NR2E3
}}{{omim
|id=604485
|rsnum=104894493
|variant=0003
}}{{ClinVar
|rsid=104894493
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=72103931
|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.72103931G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604485.0003
|CLNSIG=5
|CLNCUI=C1849394
|CLNDBN=Enhanced s-cone syndrome
|Disease=Enhanced s-cone syndrome
|CLNACC=RCV000005867.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849394:268100:53540
}}