rs11880198
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11880198(A;A) |
| Make rs11880198(A;G) |
| Make rs11880198(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 3159771 |
| Gene | GNA15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11880198 |
| dbSNP (classic) | rs11880198 |
| ClinGen | rs11880198 |
| ebi | rs11880198 |
| HLI | rs11880198 |
| Exac | rs11880198 |
| Gnomad | rs11880198 |
| Varsome | rs11880198 |
| LitVar | rs11880198 |
| Map | rs11880198 |
| PheGenI | rs11880198 |
| Biobank | rs11880198 |
| 1000 genomes | rs11880198 |
| hgdp | rs11880198 |
| ensembl | rs11880198 |
| geneview | rs11880198 |
| scholar | rs11880198 |
| rs11880198 | |
| pharmgkb | rs11880198 |
| gwascentral | rs11880198 |
| openSNP | rs11880198 |
| 23andMe | rs11880198 |
| SNPshot | rs11880198 |
| SNPdbe | rs11880198 |
| MSV3d | rs11880198 |
| GWAS Ctlg | rs11880198 |
| GMAF | 0.1433 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20445134 ]
|
| Trait | Heart failure |
| Title | The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | 1.23 [0.98-1.54] |
