rs563519
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs563519(C;C) |
| Make rs563519(C;T) |
| Make rs563519(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 126158822 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs563519 |
| dbSNP (classic) | rs563519 |
| ClinGen | rs563519 |
| ebi | rs563519 |
| HLI | rs563519 |
| Exac | rs563519 |
| Gnomad | rs563519 |
| Varsome | rs563519 |
| LitVar | rs563519 |
| Map | rs563519 |
| PheGenI | rs563519 |
| Biobank | rs563519 |
| 1000 genomes | rs563519 |
| hgdp | rs563519 |
| ensembl | rs563519 |
| geneview | rs563519 |
| scholar | rs563519 |
| rs563519 | |
| pharmgkb | rs563519 |
| gwascentral | rs563519 |
| openSNP | rs563519 |
| 23andMe | rs563519 |
| SNPshot | rs563519 |
| SNPdbe | rs563519 |
| MSV3d | rs563519 |
| GWAS Ctlg | rs563519 |
| GMAF | 0.4486 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 0.000003 |
| Odds Ratio | 1.45 [0.97-2.17] |
