rs10510829
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10510829(A;A) |
| Make rs10510829(A;G) |
| Make rs10510829(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 60137795 |
| Gene | FHIT |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10510829 |
| dbSNP (classic) | rs10510829 |
| ClinGen | rs10510829 |
| ebi | rs10510829 |
| HLI | rs10510829 |
| Exac | rs10510829 |
| Gnomad | rs10510829 |
| Varsome | rs10510829 |
| LitVar | rs10510829 |
| Map | rs10510829 |
| PheGenI | rs10510829 |
| Biobank | rs10510829 |
| 1000 genomes | rs10510829 |
| hgdp | rs10510829 |
| ensembl | rs10510829 |
| geneview | rs10510829 |
| scholar | rs10510829 |
| rs10510829 | |
| pharmgkb | rs10510829 |
| gwascentral | rs10510829 |
| openSNP | rs10510829 |
| 23andMe | rs10510829 |
| SNPshot | rs10510829 |
| SNPdbe | rs10510829 |
| MSV3d | rs10510829 |
| GWAS Ctlg | rs10510829 |
| GMAF | 0.1437 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | 7E-7 |
| Odds Ratio | None None |
