rs2046383
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2046383(G;G) |
| Make rs2046383(G;T) |
| Make rs2046383(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 29951209 |
| Gene | LOC105369715 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2046383 |
| dbSNP (classic) | rs2046383 |
| ClinGen | rs2046383 |
| ebi | rs2046383 |
| HLI | rs2046383 |
| Exac | rs2046383 |
| Gnomad | rs2046383 |
| Varsome | rs2046383 |
| LitVar | rs2046383 |
| Map | rs2046383 |
| PheGenI | rs2046383 |
| Biobank | rs2046383 |
| 1000 genomes | rs2046383 |
| hgdp | rs2046383 |
| ensembl | rs2046383 |
| geneview | rs2046383 |
| scholar | rs2046383 |
| rs2046383 | |
| pharmgkb | rs2046383 |
| gwascentral | rs2046383 |
| openSNP | rs2046383 |
| 23andMe | rs2046383 |
| SNPshot | rs2046383 |
| SNPdbe | rs2046383 |
| MSV3d | rs2046383 |
| GWAS Ctlg | rs2046383 |
| GMAF | 0.2948 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | 0.000003 |
| Odds Ratio | 1.39 [0.97-1.97] |
