rs17779747
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17779747(G;G) |
| Make rs17779747(G;T) |
| Make rs17779747(T;T) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 17 |
| Position | 70498851 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17779747 |
| dbSNP (classic) | rs17779747 |
| ClinGen | rs17779747 |
| ebi | rs17779747 |
| HLI | rs17779747 |
| Exac | rs17779747 |
| Gnomad | rs17779747 |
| Varsome | rs17779747 |
| LitVar | rs17779747 |
| Map | rs17779747 |
| PheGenI | rs17779747 |
| Biobank | rs17779747 |
| 1000 genomes | rs17779747 |
| hgdp | rs17779747 |
| ensembl | rs17779747 |
| geneview | rs17779747 |
| scholar | rs17779747 |
| rs17779747 | |
| pharmgkb | rs17779747 |
| gwascentral | rs17779747 |
| openSNP | rs17779747 |
| 23andMe | rs17779747 |
| SNPshot | rs17779747 |
| SNPdbe | rs17779747 |
| MSV3d | rs17779747 |
| GWAS Ctlg | rs17779747 |
| GMAF | 0.1974 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19305409 ]
|
| Trait | QT interval |
| Title | Common variants at ten loci modulate the QT interval duration in the QTSCD Study |
| Risk Allele | T |
| P-val | 6E-12 |
| Odds Ratio | 1.02 [0.53-1.51] ms decrease |
[PMID 19305408] Common variants at ten loci influence QT interval duration in the QTGEN Study.
[PMID 25819866] Genetic markers of repolarization and arrhythmic events after acute coronary syndromes
