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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
ebirs1990622
HLIrs1990622
Exacrs1990622
Varsomers1990622
Maprs1990622
PheGenIrs1990622
hapmaprs1990622
1000 genomesrs1990622
hgdprs1990622
ensemblrs1990622
gopubmedrs1990622
geneviewrs1990622
scholarrs1990622
googlers1990622
pharmgkbrs1990622
gwascentralrs1990622
openSNPrs1990622
23andMers1990622
23andMe allrs1990622
SNP Nexus

SNPshotrs1990622
SNPdbers1990622
MSV3drs1990622
GWAS Ctlgrs1990622
GMAF0.4389
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24385136OA-icon.png] TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

[PMID 24343233] Effect of TMEM106B polymorphism on functional network connectivity in asymptomatic GRN mutation carriers.

[PMID 24166182] TMEM106B and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in Han Chinese

[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

[PMID 21178100OA-icon.png] TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

[PMID 20154673OA-icon.png] Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions


[PMID 24770881OA-icon.png] ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology


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


[PMID 25653292] The TMEM106B locus and TDP-43 pathology in older persons without FTLD


[PMID 25470345] Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology