rs1881747
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 1.24x increased risk for LOAD | |
| (C;T) | 1.24x increased risk for LOAD | |
| (T;T) | normal |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 52573815 |
| Gene | LOC105378305 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1881747 |
| dbSNP (classic) | rs1881747 |
| ClinGen | rs1881747 |
| ebi | rs1881747 |
| HLI | rs1881747 |
| Exac | rs1881747 |
| Gnomad | rs1881747 |
| Varsome | rs1881747 |
| LitVar | rs1881747 |
| Map | rs1881747 |
| PheGenI | rs1881747 |
| Biobank | rs1881747 |
| 1000 genomes | rs1881747 |
| hgdp | rs1881747 |
| ensembl | rs1881747 |
| geneview | rs1881747 |
| scholar | rs1881747 |
| rs1881747 | |
| pharmgkb | rs1881747 |
| gwascentral | rs1881747 |
| openSNP | rs1881747 |
| 23andMe | rs1881747 |
| SNPshot | rs1881747 |
| SNPdbe | rs1881747 |
| MSV3d | rs1881747 |
| GWAS Ctlg | rs1881747 |
| GMAF | 0.4757 |
| 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 1.24, p=0.011) in a study of ~1000 Caucasian patients, but it would not have withstood statistical correction for multiple testing. [PMID 18163421]
[PMID 21281506
] A unified framework for multi-locus association analysis of both common and rare variants.
