{{Rsnum
|rsid=63749877
|Chromosome=17
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CACT)
|geno3=(CACT;CACT)
|Gene=GRN
|position=44351141
|Gene_s=GRN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=17
|CLNACC=RCV000017393.23; RCV000017394.26; RCV000029169.26; RCV000084585.1
|CLNALLE=1
|CLNDBN=Frontotemporal dementia, ubiquitin-positive; Primary progressive aphasia; Ceroid lipofuscinosis, neuronal, 11; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1371:C1843792:607485:100070:282; CN130362:614706:314629:79262
|CLNHGVS=NC_000017.10:g.42428509_42428512delCACT
|CLNSIG=5
|CLNSRC=Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNSRCID=ADM_318; 138945.0015
|Disease=Frontotemporal dementia; Primary progressive aphasia; Ceroid lipofuscinosis; not provided
|FwdREF=CACT
|GENEINFO=GRN:2896
|GENE_ID=2896
|GENE_NAME=GRN
|REF=TCACT
|RSPOS=42428508
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050160000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=63749877
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}