{{Rsnum
|rsid=104894463
|Chromosome=14
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NRL
|position=24081471
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NRL
}}{{omim
|id=162080
|rsnum=104894463
|variant=0003
}}{{ClinVar
|rsid=104894463
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=24550680
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NRL:4901
|GENE_NAME=NRL
|GENE_ID=4901
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.24550680A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015088.24
|CLNDBN=Retinal degeneration, autosomal recessive, clumped pigment type
|CLNDSDB=MedGen
|CLNDSDBID=C1834330
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=162080.0003
|Disease=Retinal degeneration
}}