rs12269901
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12269901(C;C) |
| Make rs12269901(C;G) |
| Make rs12269901(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 117103213 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12269901 |
| dbSNP (classic) | rs12269901 |
| ClinGen | rs12269901 |
| ebi | rs12269901 |
| HLI | rs12269901 |
| Exac | rs12269901 |
| Gnomad | rs12269901 |
| Varsome | rs12269901 |
| LitVar | rs12269901 |
| Map | rs12269901 |
| PheGenI | rs12269901 |
| Biobank | rs12269901 |
| 1000 genomes | rs12269901 |
| hgdp | rs12269901 |
| ensembl | rs12269901 |
| geneview | rs12269901 |
| scholar | rs12269901 |
| rs12269901 | |
| pharmgkb | rs12269901 |
| gwascentral | rs12269901 |
| openSNP | rs12269901 |
| 23andMe | rs12269901 |
| SNPshot | rs12269901 |
| SNPdbe | rs12269901 |
| MSV3d | rs12269901 |
| GWAS Ctlg | rs12269901 |
| GMAF | 0.3949 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 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 | C |
| P-val | 0.000002 |
| Odds Ratio | 0.0690 [0.04-0.10] SD increase |
