{{Rsnum
|rsid=9897526
|Gene=GRN
|Chromosome=17
|position=44349572
|Orientation=plus
|GMAF=0.1864
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GRN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 18.8 | 81.2
| HCB | 0.0 | 17.3 | 82.7
| JPT | 0.0 | 18.9 | 81.1
| YRI | 17.0 | 54.4 | 28.6
| ASW | 8.8 | 54.4 | 36.8
| CHB | 0.0 | 17.3 | 82.7
| CHD | 0.9 | 24.8 | 74.3
| GIH | 7.9 | 58.4 | 33.7
| LWK | 25.7 | 52.3 | 22.0
| MEX | 0.0 | 27.6 | 72.4
| MKK | 14.7 | 51.3 | 34.0
| TSI | 3.9 | 27.5 | 68.6
| HapMapRevision=28
}}

Associated with risk of amyotrophic lateral sclerosis ([[ALS]]) in two European populations {{PMID|18184915}}

{{ neighbor
| rsid = 34424835
| distance = 609
}}

{{omim
|desc=GRANULIN PRECURSOR; GRN
|id=138945
|rsnum=9897526
}}

{{PMID Auto
|PMID=20711061
|Title=Prion Protein Codon 129 Polymorphism Modifies Age at Onset of Frontotemporal Dementia With the C.709-1G&gt;A Progranulin Mutation
|OA=1
}}

{{PMID Auto
|PMID=18192287
|Title=Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.
}}

{{PMID Auto
|PMID=19625741
|Title=Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
|OA=1
}}

{{PMID Auto
|PMID=19640594
|Title=Recent insights into the molecular genetics of dementia.
|OA=1
}}

{{PMID Auto
|PMID=21343707
|Title=MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}