rs4979906
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4979906(A;A) |
| Make rs4979906(A;G) |
| Make rs4979906(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 77684995 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4979906 |
| dbSNP (classic) | rs4979906 |
| ClinGen | rs4979906 |
| ebi | rs4979906 |
| HLI | rs4979906 |
| Exac | rs4979906 |
| Gnomad | rs4979906 |
| Varsome | rs4979906 |
| LitVar | rs4979906 |
| Map | rs4979906 |
| PheGenI | rs4979906 |
| Biobank | rs4979906 |
| 1000 genomes | rs4979906 |
| hgdp | rs4979906 |
| ensembl | rs4979906 |
| geneview | rs4979906 |
| scholar | rs4979906 |
| rs4979906 | |
| pharmgkb | rs4979906 |
| gwascentral | rs4979906 |
| openSNP | rs4979906 |
| 23andMe | rs4979906 |
| SNPshot | rs4979906 |
| SNPdbe | rs4979906 |
| MSV3d | rs4979906 |
| GWAS Ctlg | rs4979906 |
| GMAF | 0.3494 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20400778 ]
|
| Trait | Mortality among heart failure patients |
| Title | Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium |
| Risk Allele | G |
| P-val | 0.000007 |
| Odds Ratio | 1.23 [0.98-1.55] |
