rs10906189
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10906189(A;A) |
| Make rs10906189(A;G) |
| Make rs10906189(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 12633062 |
| Gene | CAMK1D |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10906189 |
| dbSNP (classic) | rs10906189 |
| ClinGen | rs10906189 |
| ebi | rs10906189 |
| HLI | rs10906189 |
| Exac | rs10906189 |
| Gnomad | rs10906189 |
| Varsome | rs10906189 |
| LitVar | rs10906189 |
| Map | rs10906189 |
| PheGenI | rs10906189 |
| Biobank | rs10906189 |
| 1000 genomes | rs10906189 |
| hgdp | rs10906189 |
| ensembl | rs10906189 |
| geneview | rs10906189 |
| scholar | rs10906189 |
| rs10906189 | |
| pharmgkb | rs10906189 |
| gwascentral | rs10906189 |
| openSNP | rs10906189 |
| 23andMe | rs10906189 |
| SNPshot | rs10906189 |
| SNPdbe | rs10906189 |
| MSV3d | rs10906189 |
| GWAS Ctlg | rs10906189 |
| GMAF | 0.4959 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 6E-6 |
| Odds Ratio | NR NR |
