{{Rsnum
|rsid=104894386
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLN5
|position=76995077
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLN5
}}{{omim
|id=608102
|rsnum=104894386
|variant=0004
}}{{ClinVar
|rsid=104894386
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=77569212
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CLN5:1203
|GENE_NAME=CLN5
|GENE_ID=1203
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000013.10:g.77569212G>A; NC_000013.10:g.77569212G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608102.0004
|CLNSIG=5
|CLNCUI=C1850442
|CLNDBN=Ceroid lipofuscinosis neuronal 5
|Disease=Ceroid lipofuscinosis neuronal 5
|CLNACC=RCV000002676.1; RCV000049946.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1850442:256731:168491:228360
}}{{PMID Auto
|PMID=21990111
|Title=Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.
}}