rs548097
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs548097(A;C) |
| Make rs548097(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 75202132 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs548097 |
| dbSNP (classic) | rs548097 |
| ClinGen | rs548097 |
| ebi | rs548097 |
| HLI | rs548097 |
| Exac | rs548097 |
| Gnomad | rs548097 |
| Varsome | rs548097 |
| LitVar | rs548097 |
| Map | rs548097 |
| PheGenI | rs548097 |
| Biobank | rs548097 |
| 1000 genomes | rs548097 |
| hgdp | rs548097 |
| ensembl | rs548097 |
| geneview | rs548097 |
| scholar | rs548097 |
| rs548097 | |
| pharmgkb | rs548097 |
| gwascentral | rs548097 |
| openSNP | rs548097 |
| 23andMe | rs548097 |
| SNPshot | rs548097 |
| SNPdbe | rs548097 |
| MSV3d | rs548097 |
| GWAS Ctlg | rs548097 |
| GMAF | 0.06198 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 6E-7 |
| Odds Ratio | 1.62 [1.00-2.63] |
