rs11889338
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs11889338(A;A) |
| Make rs11889338(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 17246318 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11889338 |
| dbSNP (classic) | rs11889338 |
| ClinGen | rs11889338 |
| ebi | rs11889338 |
| HLI | rs11889338 |
| Exac | rs11889338 |
| Gnomad | rs11889338 |
| Varsome | rs11889338 |
| LitVar | rs11889338 |
| Map | rs11889338 |
| PheGenI | rs11889338 |
| Biobank | rs11889338 |
| 1000 genomes | rs11889338 |
| hgdp | rs11889338 |
| ensembl | rs11889338 |
| geneview | rs11889338 |
| scholar | rs11889338 |
| rs11889338 | |
| pharmgkb | rs11889338 |
| gwascentral | rs11889338 |
| openSNP | rs11889338 |
| 23andMe | rs11889338 |
| SNPshot | rs11889338 |
| SNPdbe | rs11889338 |
| MSV3d | rs11889338 |
| GWAS Ctlg | rs11889338 |
| GMAF | 0.1152 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22159054 ]
|
| Trait | |
| Title | A comprehensive genetic association study of Alzheimer disease in African Americans. |
| Risk Allele | A |
| P-val | 0.000009 |
| Odds Ratio | 1.5500 None |
