rs744487
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs744487(G;G) |
| Make rs744487(G;T) |
| Make rs744487(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 234590266 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs744487 |
| dbSNP (classic) | rs744487 |
| ClinGen | rs744487 |
| ebi | rs744487 |
| HLI | rs744487 |
| Exac | rs744487 |
| Gnomad | rs744487 |
| Varsome | rs744487 |
| LitVar | rs744487 |
| Map | rs744487 |
| PheGenI | rs744487 |
| Biobank | rs744487 |
| 1000 genomes | rs744487 |
| hgdp | rs744487 |
| ensembl | rs744487 |
| geneview | rs744487 |
| scholar | rs744487 |
| rs744487 | |
| pharmgkb | rs744487 |
| gwascentral | rs744487 |
| openSNP | rs744487 |
| 23andMe | rs744487 |
| SNPshot | rs744487 |
| SNPdbe | rs744487 |
| MSV3d | rs744487 |
| GWAS Ctlg | rs744487 |
| GMAF | 0.2746 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21347282 ]
|
| Trait | |
| Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
| Risk Allele | A |
| P-val | 0.000005 |
| Odds Ratio | 0.0690 [0.04-0.10] SD decrease |
