rs6473383
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6473383(A;A) |
| Make rs6473383(A;G) |
| Make rs6473383(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 82756885 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6473383 |
| dbSNP (classic) | rs6473383 |
| ClinGen | rs6473383 |
| ebi | rs6473383 |
| HLI | rs6473383 |
| Exac | rs6473383 |
| Gnomad | rs6473383 |
| Varsome | rs6473383 |
| LitVar | rs6473383 |
| Map | rs6473383 |
| PheGenI | rs6473383 |
| Biobank | rs6473383 |
| 1000 genomes | rs6473383 |
| hgdp | rs6473383 |
| ensembl | rs6473383 |
| geneview | rs6473383 |
| scholar | rs6473383 |
| rs6473383 | |
| pharmgkb | rs6473383 |
| gwascentral | rs6473383 |
| openSNP | rs6473383 |
| 23andMe | rs6473383 |
| SNPshot | rs6473383 |
| SNPdbe | rs6473383 |
| MSV3d | rs6473383 |
| GWAS Ctlg | rs6473383 |
| GMAF | 0.1501 |
| 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 | 0.000003 |
| Odds Ratio | 1.19 [0.99-1.44] |
