rs11166827
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11166827(C;C) |
| Make rs11166827(C;T) |
| Make rs11166827(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 138492027 |
| Gene | FAM135B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11166827 |
| dbSNP (classic) | rs11166827 |
| ClinGen | rs11166827 |
| ebi | rs11166827 |
| HLI | rs11166827 |
| Exac | rs11166827 |
| Gnomad | rs11166827 |
| Varsome | rs11166827 |
| LitVar | rs11166827 |
| Map | rs11166827 |
| PheGenI | rs11166827 |
| Biobank | rs11166827 |
| 1000 genomes | rs11166827 |
| hgdp | rs11166827 |
| ensembl | rs11166827 |
| geneview | rs11166827 |
| scholar | rs11166827 |
| rs11166827 | |
| pharmgkb | rs11166827 |
| gwascentral | rs11166827 |
| openSNP | rs11166827 |
| 23andMe | rs11166827 |
| SNPshot | rs11166827 |
| SNPdbe | rs11166827 |
| MSV3d | rs11166827 |
| GWAS Ctlg | rs11166827 |
| GMAF | 0.4073 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20125193 ]
|
| Trait | Cognitive performance |
| Title | Common genetic variation and performance on standardized cognitive tests. |
| Risk Allele | |
| P-val | 5E-6 |
| Odds Ratio | NR NR |
