rs6590322
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6590322(C;C) |
| Make rs6590322(C;T) |
| Make rs6590322(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 128336515 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6590322 |
| dbSNP (classic) | rs6590322 |
| ClinGen | rs6590322 |
| ebi | rs6590322 |
| HLI | rs6590322 |
| Exac | rs6590322 |
| Gnomad | rs6590322 |
| Varsome | rs6590322 |
| LitVar | rs6590322 |
| Map | rs6590322 |
| PheGenI | rs6590322 |
| Biobank | rs6590322 |
| 1000 genomes | rs6590322 |
| hgdp | rs6590322 |
| ensembl | rs6590322 |
| geneview | rs6590322 |
| scholar | rs6590322 |
| rs6590322 | |
| pharmgkb | rs6590322 |
| gwascentral | rs6590322 |
| openSNP | rs6590322 |
| 23andMe | rs6590322 |
| SNPshot | rs6590322 |
| SNPdbe | rs6590322 |
| MSV3d | rs6590322 |
| GWAS Ctlg | rs6590322 |
| GMAF | 0.4931 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 0.000009 |
| Odds Ratio | NR NR |
