rs11626056
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11626056(C;C) |
| Make rs11626056(C;T) |
| Make rs11626056(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 51766558 |
| Gene | LOC101927598 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11626056 |
| dbSNP (classic) | rs11626056 |
| ClinGen | rs11626056 |
| ebi | rs11626056 |
| HLI | rs11626056 |
| Exac | rs11626056 |
| Gnomad | rs11626056 |
| Varsome | rs11626056 |
| LitVar | rs11626056 |
| Map | rs11626056 |
| PheGenI | rs11626056 |
| Biobank | rs11626056 |
| 1000 genomes | rs11626056 |
| hgdp | rs11626056 |
| ensembl | rs11626056 |
| geneview | rs11626056 |
| scholar | rs11626056 |
| rs11626056 | |
| pharmgkb | rs11626056 |
| gwascentral | rs11626056 |
| openSNP | rs11626056 |
| 23andMe | rs11626056 |
| SNPshot | rs11626056 |
| SNPdbe | rs11626056 |
| MSV3d | rs11626056 |
| GWAS Ctlg | rs11626056 |
| GMAF | 0.3292 |
| 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 | 0.000001 |
| Odds Ratio | NR NR |
