rs13225783
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs13225783(C;T) |
| Make rs13225783(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 27290437 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13225783 |
| dbSNP (classic) | rs13225783 |
| ClinGen | rs13225783 |
| ebi | rs13225783 |
| HLI | rs13225783 |
| Exac | rs13225783 |
| Gnomad | rs13225783 |
| Varsome | rs13225783 |
| LitVar | rs13225783 |
| Map | rs13225783 |
| PheGenI | rs13225783 |
| Biobank | rs13225783 |
| 1000 genomes | rs13225783 |
| hgdp | rs13225783 |
| ensembl | rs13225783 |
| geneview | rs13225783 |
| scholar | rs13225783 |
| rs13225783 | |
| pharmgkb | rs13225783 |
| gwascentral | rs13225783 |
| openSNP | rs13225783 |
| 23andMe | rs13225783 |
| SNPshot | rs13225783 |
| SNPdbe | rs13225783 |
| MSV3d | rs13225783 |
| GWAS Ctlg | rs13225783 |
| GMAF | 0.02112 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | 0.000007 |
| Odds Ratio | 1.38 [0.96-1.99] |
