{{Rsnum
|rsid=104894064
|Chromosome=8
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CLN8
|position=1771124
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLN8
}}{{omim
|id=607837
|rsnum=104894064
|variant=0001
}}{{ClinVar
|rsid=104894064
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=1719290
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CLN8:2055
|GENE_NAME=CLN8
|GENE_ID=2055
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.1719290C>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1428; 607837.0001
|CLNSIG=5
|CLNCUI=C1864923
|CLNDBN=Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant
|Disease=Ceroid lipofuscinosis
|CLNACC=RCV000002936.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1428:C1864923:610003:1947
}}