rs17019682
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs17019682(A;T) |
| Make rs17019682(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 91911494 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17019682 |
| dbSNP (classic) | rs17019682 |
| ClinGen | rs17019682 |
| ebi | rs17019682 |
| HLI | rs17019682 |
| Exac | rs17019682 |
| Gnomad | rs17019682 |
| Varsome | rs17019682 |
| LitVar | rs17019682 |
| Map | rs17019682 |
| PheGenI | rs17019682 |
| Biobank | rs17019682 |
| 1000 genomes | rs17019682 |
| hgdp | rs17019682 |
| ensembl | rs17019682 |
| geneview | rs17019682 |
| scholar | rs17019682 |
| rs17019682 | |
| pharmgkb | rs17019682 |
| gwascentral | rs17019682 |
| openSNP | rs17019682 |
| 23andMe | rs17019682 |
| SNPshot | rs17019682 |
| SNPdbe | rs17019682 |
| MSV3d | rs17019682 |
| GWAS Ctlg | rs17019682 |
| GMAF | 0.06566 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | 0.000002 |
| Odds Ratio | 1.47 [0.98-2.22] |
