Rs11626056
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11626056 |
| PheGenI | rs11626056 |
| nextbio | rs11626056 |
| hapmap | rs11626056 |
| 1000 genomes | rs11626056 |
| hgdp | rs11626056 |
| ensembl | rs11626056 |
| gopubmed | rs11626056 |
| geneview | rs11626056 |
| scholar | rs11626056 |
| rs11626056 | |
| pharmgkb | rs11626056 |
| gwascentral | rs11626056 |
| openSNP | rs11626056 |
| 23andMe | rs11626056 |
| 23andMe all | rs11626056 |
| SNP Nexus | |
| SNPshot | rs11626056 |
| SNPdbe | rs11626056 |
| MSV3d | rs11626056 |
| Chromosome | 14 |
| Orientation | plus |
| GMAF | 0.3292 |
| Position | 52233276 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs11626056(C;C) |
| Make rs11626056(C;T) |
| Make rs11626056(T;T) |
| ? | (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 |
| GET Evidence | |
|---|---|
| rs11626056 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.201923 |
| summary | |
