rs5030882
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 1 | |
(C;T) | ||
(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 68692714 |
Gene | TET1 |
is a | snp |
is | mentioned by |
dbSNP | rs5030882 |
dbSNP (classic) | rs5030882 |
ClinGen | rs5030882 |
ebi | rs5030882 |
HLI | rs5030882 |
Exac | rs5030882 |
Gnomad | rs5030882 |
Varsome | rs5030882 |
LitVar | rs5030882 |
Map | rs5030882 |
PheGenI | rs5030882 |
Biobank | rs5030882 |
1000 genomes | rs5030882 |
hgdp | rs5030882 |
ensembl | rs5030882 |
geneview | rs5030882 |
scholar | rs5030882 |
rs5030882 | |
pharmgkb | rs5030882 |
gwascentral | rs5030882 |
openSNP | rs5030882 |
23andMe | rs5030882 |
SNPshot | rs5030882 |
SNPdbe | rs5030882 |
MSV3d | rs5030882 |
GWAS Ctlg | rs5030882 |
GMAF | 0.1001 |
Max Magnitude | 1 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio 1.29, p=0.046) in a study of ~1000 Caucasian patients, but it would not have withstood statistical correction for multiple testing. [PMID 18163421]