rs1569476
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1569476(A;A) |
| Make rs1569476(A;G) |
| Make rs1569476(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169639679 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1569476 |
| dbSNP (classic) | rs1569476 |
| ClinGen | rs1569476 |
| ebi | rs1569476 |
| HLI | rs1569476 |
| Exac | rs1569476 |
| Gnomad | rs1569476 |
| Varsome | rs1569476 |
| LitVar | rs1569476 |
| Map | rs1569476 |
| PheGenI | rs1569476 |
| Biobank | rs1569476 |
| 1000 genomes | rs1569476 |
| hgdp | rs1569476 |
| ensembl | rs1569476 |
| geneview | rs1569476 |
| scholar | rs1569476 |
| rs1569476 | |
| pharmgkb | rs1569476 |
| gwascentral | rs1569476 |
| openSNP | rs1569476 |
| 23andMe | rs1569476 |
| SNPshot | rs1569476 |
| SNPdbe | rs1569476 |
| MSV3d | rs1569476 |
| GWAS Ctlg | rs1569476 |
| GMAF | 0.2888 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21116278 ]
|
| Trait | |
| Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
| Risk Allele | |
| P-val | 3E-7 |
| Odds Ratio | 0.0032 [NR] unit increase (main effect) |
