rs4528684
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs4528684(C;T) |
| Make rs4528684(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 14240762 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4528684 |
| dbSNP (classic) | rs4528684 |
| ClinGen | rs4528684 |
| ebi | rs4528684 |
| HLI | rs4528684 |
| Exac | rs4528684 |
| Gnomad | rs4528684 |
| Varsome | rs4528684 |
| LitVar | rs4528684 |
| Map | rs4528684 |
| PheGenI | rs4528684 |
| Biobank | rs4528684 |
| 1000 genomes | rs4528684 |
| hgdp | rs4528684 |
| ensembl | rs4528684 |
| geneview | rs4528684 |
| scholar | rs4528684 |
| rs4528684 | |
| pharmgkb | rs4528684 |
| gwascentral | rs4528684 |
| openSNP | rs4528684 |
| 23andMe | rs4528684 |
| SNPshot | rs4528684 |
| SNPdbe | rs4528684 |
| MSV3d | rs4528684 |
| GWAS Ctlg | rs4528684 |
| GMAF | 0.101 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20400778 ]
|
| Trait | Mortality among heart failure patients |
| Title | Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium |
| Risk Allele | T |
| P-val | 0.000001 |
| Odds Ratio | 1.42 [0.99-2.03] |
