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rs9897526

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9897526(A;A)
Make rs9897526(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position44349572
GeneGRN
is asnp
is mentioned by
dbSNPrs9897526
ebirs9897526
HLIrs9897526
Exacrs9897526
Varsomers9897526
Maprs9897526
PheGenIrs9897526
hapmaprs9897526
1000 genomesrs9897526
hgdprs9897526
ensemblrs9897526
gopubmedrs9897526
geneviewrs9897526
scholarrs9897526
googlers9897526
pharmgkbrs9897526
gwascentralrs9897526
openSNPrs9897526
23andMers9897526
23andMe allrs9897526
SNP Nexus

SNPshotrs9897526
SNPdbers9897526
MSV3drs9897526
GWAS Ctlgrs9897526
GMAF0.1864
Max Magnitude0
? (A;A) (A;G) (G;G) 28

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

Neighborrs34424835
Distance609
OMIM138945
DescGRANULIN PRECURSOR; GRN
Variant
Relatedalso
[PMID 20711061OA-icon.png] Prion Protein Codon 129 Polymorphism Modifies Age at Onset of Frontotemporal Dementia With the C.709-1G>A Progranulin Mutation


[PMID 18192287] 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 19625741OA-icon.png] Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.


[PMID 19640594OA-icon.png] Recent insights into the molecular genetics of dementia.


[PMID 21343707] MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?