rs7009219
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7009219(C;C) |
| Make rs7009219(C;T) |
| Make rs7009219(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 52301705 |
| Gene | ST18 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7009219 |
| dbSNP (classic) | rs7009219 |
| ClinGen | rs7009219 |
| ebi | rs7009219 |
| HLI | rs7009219 |
| Exac | rs7009219 |
| Gnomad | rs7009219 |
| Varsome | rs7009219 |
| LitVar | rs7009219 |
| Map | rs7009219 |
| PheGenI | rs7009219 |
| Biobank | rs7009219 |
| 1000 genomes | rs7009219 |
| hgdp | rs7009219 |
| ensembl | rs7009219 |
| geneview | rs7009219 |
| scholar | rs7009219 |
| rs7009219 | |
| pharmgkb | rs7009219 |
| gwascentral | rs7009219 |
| openSNP | rs7009219 |
| 23andMe | rs7009219 |
| SNPshot | rs7009219 |
| SNPdbe | rs7009219 |
| MSV3d | rs7009219 |
| GWAS Ctlg | rs7009219 |
| GMAF | 0.1754 |
| 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 | 5E-7 |
| Odds Ratio | .16 unit decrease |
