rs2279420
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0.79x decreased risk for LOAD | |
| (C;T) | 0.79x decreased risk for LOAD | |
| (T;T) | 0 | normal |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 60022189 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2279420 |
| dbSNP (classic) | rs2279420 |
| ClinGen | rs2279420 |
| ebi | rs2279420 |
| HLI | rs2279420 |
| Exac | rs2279420 |
| Gnomad | rs2279420 |
| Varsome | rs2279420 |
| LitVar | rs2279420 |
| Map | rs2279420 |
| PheGenI | rs2279420 |
| Biobank | rs2279420 |
| 1000 genomes | rs2279420 |
| hgdp | rs2279420 |
| ensembl | rs2279420 |
| geneview | rs2279420 |
| scholar | rs2279420 |
| rs2279420 | |
| pharmgkb | rs2279420 |
| gwascentral | rs2279420 |
| openSNP | rs2279420 |
| 23andMe | rs2279420 |
| SNPshot | rs2279420 |
| SNPdbe | rs2279420 |
| MSV3d | rs2279420 |
| GWAS Ctlg | rs2279420 |
| GMAF | 0.07759 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Nominally significant association found for this SNP with late-onset Alzheimer's disease (odds ratio 0.79, p=0.022) in a study of ~1000 Caucasian patients, but it would not have withstood statistical correction for multiple testing. [PMID 18163421]
