rs17767225
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17767225(C;C) |
| Make rs17767225(C;T) |
| Make rs17767225(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 71199580 |
| Gene | LOC105370706 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17767225 |
| dbSNP (classic) | rs17767225 |
| ClinGen | rs17767225 |
| ebi | rs17767225 |
| HLI | rs17767225 |
| Exac | rs17767225 |
| Gnomad | rs17767225 |
| Varsome | rs17767225 |
| LitVar | rs17767225 |
| Map | rs17767225 |
| PheGenI | rs17767225 |
| Biobank | rs17767225 |
| 1000 genomes | rs17767225 |
| hgdp | rs17767225 |
| ensembl | rs17767225 |
| geneview | rs17767225 |
| scholar | rs17767225 |
| rs17767225 | |
| pharmgkb | rs17767225 |
| gwascentral | rs17767225 |
| openSNP | rs17767225 |
| 23andMe | rs17767225 |
| SNPshot | rs17767225 |
| SNPdbe | rs17767225 |
| MSV3d | rs17767225 |
| GWAS Ctlg | rs17767225 |
| GMAF | 0.07943 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22881374 ]
|
| Trait | Alzheimer's disease (late onset) |
| Title | Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. |
| Risk Allele | T |
| P-val | 8E-6 |
| Odds Ratio | NR NR |
