rs17301739
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17301739(C;C) |
| Make rs17301739(C;G) |
| Make rs17301739(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 58438440 |
| Gene | LIPC, LIPC-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17301739 |
| dbSNP (classic) | rs17301739 |
| ClinGen | rs17301739 |
| ebi | rs17301739 |
| HLI | rs17301739 |
| Exac | rs17301739 |
| Gnomad | rs17301739 |
| Varsome | rs17301739 |
| LitVar | rs17301739 |
| Map | rs17301739 |
| PheGenI | rs17301739 |
| Biobank | rs17301739 |
| 1000 genomes | rs17301739 |
| hgdp | rs17301739 |
| ensembl | rs17301739 |
| geneview | rs17301739 |
| scholar | rs17301739 |
| rs17301739 | |
| pharmgkb | rs17301739 |
| gwascentral | rs17301739 |
| openSNP | rs17301739 |
| 23andMe | rs17301739 |
| SNPshot | rs17301739 |
| SNPdbe | rs17301739 |
| MSV3d | rs17301739 |
| GWAS Ctlg | rs17301739 |
| GMAF | 0.07117 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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 | 2E-6 |
| Odds Ratio | .28 unit decrease |
