rs12449964
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12449964(C;C) |
| Make rs12449964(C;T) |
| Make rs12449964(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 17641390 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12449964 |
| dbSNP (classic) | rs12449964 |
| ClinGen | rs12449964 |
| ebi | rs12449964 |
| HLI | rs12449964 |
| Exac | rs12449964 |
| Gnomad | rs12449964 |
| Varsome | rs12449964 |
| LitVar | rs12449964 |
| Map | rs12449964 |
| PheGenI | rs12449964 |
| Biobank | rs12449964 |
| 1000 genomes | rs12449964 |
| hgdp | rs12449964 |
| ensembl | rs12449964 |
| geneview | rs12449964 |
| scholar | rs12449964 |
| rs12449964 | |
| pharmgkb | rs12449964 |
| gwascentral | rs12449964 |
| openSNP | rs12449964 |
| 23andMe | rs12449964 |
| SNPshot | rs12449964 |
| SNPdbe | rs12449964 |
| MSV3d | rs12449964 |
| GWAS Ctlg | rs12449964 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24262325 ]
|
| Trait | Coronary artery disease or ischemic stroke |
| Title | Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. |
| Risk Allele | |
| P-val | 2E-8 |
| Odds Ratio | NR NR |
