rs1990622
Orientation | minus |
Stabilized | minus |
Make rs1990622(C;C) |
Make rs1990622(C;T) |
Make rs1990622(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 12244161 |
is a | snp |
is | mentioned by |
dbSNP | rs1990622 |
dbSNP (classic) | rs1990622 |
ClinGen | rs1990622 |
ebi | rs1990622 |
HLI | rs1990622 |
Exac | rs1990622 |
Gnomad | rs1990622 |
Varsome | rs1990622 |
LitVar | rs1990622 |
Map | rs1990622 |
PheGenI | rs1990622 |
Biobank | rs1990622 |
1000 genomes | rs1990622 |
hgdp | rs1990622 |
ensembl | rs1990622 |
geneview | rs1990622 |
scholar | rs1990622 |
rs1990622 | |
pharmgkb | rs1990622 |
gwascentral | rs1990622 |
openSNP | rs1990622 |
23andMe | rs1990622 |
SNPshot | rs1990622 |
SNPdbe | rs1990622 |
MSV3d | rs1990622 |
GWAS Ctlg | rs1990622 |
GMAF | 0.4389 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24385136] 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 23742080] TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia
[PMID 21354975] TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.
[PMID 21220649] Association of TMEM106B Gene Polymorphism With Age at Onset in Granulin Mutation Carriers and Plasma Granulin Protein Levels
[PMID 21178100] TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
[PMID 20154673] Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
[PMID 24770881] 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
[PMID 28189700] CSF protein changes associated with hippocampal sclerosis risk gene variants highlight impact of GRN/PGRN.
[PMID 28441426] Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data.
[PMID 30973966] TMEM106B Effect on Cognition in Parkinson's Disease and Frontotemporal Dementia.