rs11154851
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs11154851(C;T) |
| Make rs11154851(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 136046867 |
| Gene | LOC644135, PDE7B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11154851 |
| dbSNP (classic) | rs11154851 |
| ClinGen | rs11154851 |
| ebi | rs11154851 |
| HLI | rs11154851 |
| Exac | rs11154851 |
| Gnomad | rs11154851 |
| Varsome | rs11154851 |
| LitVar | rs11154851 |
| Map | rs11154851 |
| PheGenI | rs11154851 |
| Biobank | rs11154851 |
| 1000 genomes | rs11154851 |
| hgdp | rs11154851 |
| ensembl | rs11154851 |
| geneview | rs11154851 |
| scholar | rs11154851 |
| rs11154851 | |
| pharmgkb | rs11154851 |
| gwascentral | rs11154851 |
| openSNP | rs11154851 |
| 23andMe | rs11154851 |
| SNPshot | rs11154851 |
| SNPdbe | rs11154851 |
| MSV3d | rs11154851 |
| GWAS Ctlg | rs11154851 |
| GMAF | 0.07851 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23535033 ]
|
| Trait | Alzheimer's disease (cognitive decline) |
| Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
| Risk Allele | |
| P-val | 1E-8 |
| Odds Ratio | .25 unit decrease |
