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rs1990622

From SNPedia

Orientationminus
Stabilizedminus
Make rs1990622(C;C)
Make rs1990622(C;T)
Make rs1990622(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position12244161
is asnp
is mentioned by
dbSNPrs1990622
dbSNP (classic)rs1990622
ClinGenrs1990622
ebirs1990622
HLIrs1990622
Exacrs1990622
Gnomadrs1990622
Varsomers1990622
LitVarrs1990622
Maprs1990622
PheGenIrs1990622
Biobankrs1990622
1000 genomesrs1990622
hgdprs1990622
ensemblrs1990622
geneviewrs1990622
scholarrs1990622
googlers1990622
pharmgkbrs1990622
gwascentralrs1990622
openSNPrs1990622
23andMers1990622
SNPshotrs1990622
SNPdbers1990622
MSV3drs1990622
GWAS Ctlgrs1990622
GMAF0.4389
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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[PMID 23742080OA-icon.png] TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

[PMID 21354975OA-icon.png] TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.

[PMID 21220649OA-icon.png] Association of TMEM106B Gene Polymorphism With Age at Onset in Granulin Mutation Carriers and Plasma Granulin Protein Levels

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[PMID 25096617] Association of TMEM106B rs1990622 Marker and Frontotemporal Dementia: Evidence for a Recessive Effect and Meta-Analysis


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[PMID 30973966OA-icon.png] TMEM106B Effect on Cognition in Parkinson's Disease and Frontotemporal Dementia.