rs12733856
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12733856(A;A) |
| Make rs12733856(A;C) |
| Make rs12733856(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 221378197 |
| Gene | LOC105372932 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12733856 |
| dbSNP (classic) | rs12733856 |
| ClinGen | rs12733856 |
| ebi | rs12733856 |
| HLI | rs12733856 |
| Exac | rs12733856 |
| Gnomad | rs12733856 |
| Varsome | rs12733856 |
| LitVar | rs12733856 |
| Map | rs12733856 |
| PheGenI | rs12733856 |
| Biobank | rs12733856 |
| 1000 genomes | rs12733856 |
| hgdp | rs12733856 |
| ensembl | rs12733856 |
| geneview | rs12733856 |
| scholar | rs12733856 |
| rs12733856 | |
| pharmgkb | rs12733856 |
| gwascentral | rs12733856 |
| openSNP | rs12733856 |
| 23andMe | rs12733856 |
| SNPshot | rs12733856 |
| SNPdbe | rs12733856 |
| MSV3d | rs12733856 |
| GWAS Ctlg | rs12733856 |
| GMAF | 0.3903 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | A |
| P-val | 0.000003 |
| Odds Ratio | 1.56 [0.97-2.51] |
