rs5904726
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5904726(A;A) |
| Make rs5904726(A;G) |
| Make rs5904726(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 147241105 |
| Gene | LOC105373347 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5904726 |
| dbSNP (classic) | rs5904726 |
| ClinGen | rs5904726 |
| ebi | rs5904726 |
| HLI | rs5904726 |
| Exac | rs5904726 |
| Gnomad | rs5904726 |
| Varsome | rs5904726 |
| LitVar | rs5904726 |
| Map | rs5904726 |
| PheGenI | rs5904726 |
| Biobank | rs5904726 |
| 1000 genomes | rs5904726 |
| hgdp | rs5904726 |
| ensembl | rs5904726 |
| geneview | rs5904726 |
| scholar | rs5904726 |
| rs5904726 | |
| pharmgkb | rs5904726 |
| gwascentral | rs5904726 |
| openSNP | rs5904726 |
| 23andMe | rs5904726 |
| SNPshot | rs5904726 |
| SNPdbe | rs5904726 |
| MSV3d | rs5904726 |
| GWAS Ctlg | rs5904726 |
| GMAF | 0.3646 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | A |
| P-val | 0.000009 |
| Odds Ratio | 0.0639 [0.03-0.09] SD increase |
