rs9326246
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9326246(C;C) |
| Make rs9326246(C;G) |
| Make rs9326246(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 116741017 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9326246 |
| dbSNP (classic) | rs9326246 |
| ClinGen | rs9326246 |
| ebi | rs9326246 |
| HLI | rs9326246 |
| Exac | rs9326246 |
| Gnomad | rs9326246 |
| Varsome | rs9326246 |
| LitVar | rs9326246 |
| Map | rs9326246 |
| PheGenI | rs9326246 |
| Biobank | rs9326246 |
| 1000 genomes | rs9326246 |
| hgdp | rs9326246 |
| ensembl | rs9326246 |
| geneview | rs9326246 |
| scholar | rs9326246 |
| rs9326246 | |
| pharmgkb | rs9326246 |
| gwascentral | rs9326246 |
| openSNP | rs9326246 |
| 23andMe | rs9326246 |
| SNPshot | rs9326246 |
| SNPdbe | rs9326246 |
| MSV3d | rs9326246 |
| GWAS Ctlg | rs9326246 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23202125
] Large-scale association analysis identifies new risk loci for coronary artery disease.
| GWAS snp | |
|---|---|
| PMID | [PMID 24262325]
|
| Trait | Coronary artery disease |
| Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
| Risk Allele | C |
| P-val | 3E-7 |
| Odds Ratio | 1.15 [1.09-1.21] |
[PMID 28106113] Genetic risk variants for metabolic traits in Arab populations.
