rs1426063
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1426063(C;C) |
| Make rs1426063(C;T) |
| Make rs1426063(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 4 |
| Position | 75105711 |
| Gene | LOC105377283 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1426063 |
| dbSNP (classic) | rs1426063 |
| ClinGen | rs1426063 |
| ebi | rs1426063 |
| HLI | rs1426063 |
| Exac | rs1426063 |
| Gnomad | rs1426063 |
| Varsome | rs1426063 |
| LitVar | rs1426063 |
| Map | rs1426063 |
| PheGenI | rs1426063 |
| Biobank | rs1426063 |
| 1000 genomes | rs1426063 |
| hgdp | rs1426063 |
| ensembl | rs1426063 |
| geneview | rs1426063 |
| scholar | rs1426063 |
| rs1426063 | |
| pharmgkb | rs1426063 |
| gwascentral | rs1426063 |
| openSNP | rs1426063 |
| 23andMe | rs1426063 |
| SNPshot | rs1426063 |
| SNPdbe | rs1426063 |
| MSV3d | rs1426063 |
| GWAS Ctlg | rs1426063 |
| GMAF | 0.1786 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23166209 ]
|
| Trait | QT interval |
| Title | Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans. |
| Risk Allele | A |
| P-val | 8E-6 |
| Odds Ratio | 1.18 [0.67-1.69] unit decrease |
