rs4845552
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4845552(A;A) |
| Make rs4845552(A;G) |
| Make rs4845552(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 153507522 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4845552 |
| dbSNP (classic) | rs4845552 |
| ClinGen | rs4845552 |
| ebi | rs4845552 |
| HLI | rs4845552 |
| Exac | rs4845552 |
| Gnomad | rs4845552 |
| Varsome | rs4845552 |
| LitVar | rs4845552 |
| Map | rs4845552 |
| PheGenI | rs4845552 |
| Biobank | rs4845552 |
| 1000 genomes | rs4845552 |
| hgdp | rs4845552 |
| ensembl | rs4845552 |
| geneview | rs4845552 |
| scholar | rs4845552 |
| rs4845552 | |
| pharmgkb | rs4845552 |
| gwascentral | rs4845552 |
| openSNP | rs4845552 |
| 23andMe | rs4845552 |
| SNPshot | rs4845552 |
| SNPdbe | rs4845552 |
| MSV3d | rs4845552 |
| GWAS Ctlg | rs4845552 |
| GMAF | 0.1272 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19668339 ]
|
| Trait | Hippocampal atrophy |
| Title | Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
