rs9919839
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9919839(C;C) |
| Make rs9919839(C;T) |
| Make rs9919839(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 71600221 |
| Gene | DACH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9919839 |
| dbSNP (classic) | rs9919839 |
| ClinGen | rs9919839 |
| ebi | rs9919839 |
| HLI | rs9919839 |
| Exac | rs9919839 |
| Gnomad | rs9919839 |
| Varsome | rs9919839 |
| LitVar | rs9919839 |
| Map | rs9919839 |
| PheGenI | rs9919839 |
| Biobank | rs9919839 |
| 1000 genomes | rs9919839 |
| hgdp | rs9919839 |
| ensembl | rs9919839 |
| geneview | rs9919839 |
| scholar | rs9919839 |
| rs9919839 | |
| pharmgkb | rs9919839 |
| gwascentral | rs9919839 |
| openSNP | rs9919839 |
| 23andMe | rs9919839 |
| SNPshot | rs9919839 |
| SNPdbe | rs9919839 |
| MSV3d | rs9919839 |
| GWAS Ctlg | rs9919839 |
| GMAF | 0.1685 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22379998 ]
|
| Trait | |
| Title | Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | None None |
