rs1612141
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1612141(C;C) |
| Make rs1612141(C;T) |
| Make rs1612141(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 41233395 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1612141 |
| dbSNP (classic) | rs1612141 |
| ClinGen | rs1612141 |
| ebi | rs1612141 |
| HLI | rs1612141 |
| Exac | rs1612141 |
| Gnomad | rs1612141 |
| Varsome | rs1612141 |
| LitVar | rs1612141 |
| Map | rs1612141 |
| PheGenI | rs1612141 |
| Biobank | rs1612141 |
| 1000 genomes | rs1612141 |
| hgdp | rs1612141 |
| ensembl | rs1612141 |
| geneview | rs1612141 |
| scholar | rs1612141 |
| rs1612141 | |
| pharmgkb | rs1612141 |
| gwascentral | rs1612141 |
| openSNP | rs1612141 |
| 23andMe | rs1612141 |
| SNPshot | rs1612141 |
| SNPdbe | rs1612141 |
| MSV3d | rs1612141 |
| GWAS Ctlg | rs1612141 |
| GMAF | 0.2259 |
| 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 | A |
| P-val | 5E-6 |
| Odds Ratio | NR NR |
