rs4569005
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4569005(C;C) |
| Make rs4569005(C;T) |
| Make rs4569005(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 21037185 |
| Gene | NELL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4569005 |
| dbSNP (classic) | rs4569005 |
| ClinGen | rs4569005 |
| ebi | rs4569005 |
| HLI | rs4569005 |
| Exac | rs4569005 |
| Gnomad | rs4569005 |
| Varsome | rs4569005 |
| LitVar | rs4569005 |
| Map | rs4569005 |
| PheGenI | rs4569005 |
| Biobank | rs4569005 |
| 1000 genomes | rs4569005 |
| hgdp | rs4569005 |
| ensembl | rs4569005 |
| geneview | rs4569005 |
| scholar | rs4569005 |
| rs4569005 | |
| pharmgkb | rs4569005 |
| gwascentral | rs4569005 |
| openSNP | rs4569005 |
| 23andMe | rs4569005 |
| SNPshot | rs4569005 |
| SNPdbe | rs4569005 |
| MSV3d | rs4569005 |
| GWAS Ctlg | rs4569005 |
| GMAF | 0.1552 |
| 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 | 0.000005 |
| Odds Ratio | None None |
