{{Rsnum
|rsid=119455955
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TPP1
|position=6617040
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPP1
}}{{omim
|id=607998
|rsnum=119455955
|variant=0003
}}{{ClinVar
|rsid=119455955
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=6638271
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040002110100
|GENEINFO=TPP1:1200
|GENE_NAME=TPP1
|GENE_ID=1200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.6638271G>A
|CLNSRC=GTR; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000330881; NBK1428; 607998.0003
|CLNSIG=5
|CLNCUI=C1876161
|CLNDBN=Ceroid lipofuscinosis, neuronal, 2
|Disease=Ceroid lipofuscinosis
|CLNACC=RCV000002762.2
|Tags=RV;PM;S3D;VLD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1876161:204500:168491:228349:79264
}}