rs7006687
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7006687(C;C) |
| Make rs7006687(C;T) |
| Make rs7006687(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 18376073 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7006687 |
| dbSNP (classic) | rs7006687 |
| ClinGen | rs7006687 |
| ebi | rs7006687 |
| HLI | rs7006687 |
| Exac | rs7006687 |
| Gnomad | rs7006687 |
| Varsome | rs7006687 |
| LitVar | rs7006687 |
| Map | rs7006687 |
| PheGenI | rs7006687 |
| Biobank | rs7006687 |
| 1000 genomes | rs7006687 |
| hgdp | rs7006687 |
| ensembl | rs7006687 |
| geneview | rs7006687 |
| scholar | rs7006687 |
| rs7006687 | |
| pharmgkb | rs7006687 |
| gwascentral | rs7006687 |
| openSNP | rs7006687 |
| 23andMe | rs7006687 |
| SNPshot | rs7006687 |
| SNPdbe | rs7006687 |
| MSV3d | rs7006687 |
| GWAS Ctlg | rs7006687 |
| GMAF | 0.4256 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23459443 ]
|
| Trait | QT interval (interaction) |
| Title | Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. |
| Risk Allele | T |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
