{{Rsnum
|rsid=63751294
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GRN
|position=44352404
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GRN
}}{{omim
|id=138945
|rsnum=63751294
|variant=0009
}}

{{ClinVar
|rsid=63751294
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=42429772
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=GRN:2896
|GENE_NAME=GRN
|GENE_ID=2896
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.42429772C>T
|CLNSRC=GeneReviews; Neurodegenerative Brain Diseases Group; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1371; ADM_297; 138945.0009
|CLNSIG=5
|CLNCUI=C1843792; C1843792
|CLNDBN=Frontotemporal dementia, ubiquitin-positive; not provided
|Disease=Frontotemporal dementia; not provided
|CLNACC=RCV000017387.26; RCV000084491.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1371:C1843792:607485:100070:282
}}

{{PMID|16983677|OA=1
}} Characteristics of frontotemporal dementia patients with a Progranulin mutation.

{{PMID|17210807}} Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

{{PMID|17522386|OA=1
}} Clinicopathologic correlation in PGRN mutations.

{{PMID|17826340}} Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

{{PMID|18703462}} Distinct genetic forms of frontotemporal dementia.

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