Rs5030862
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5030862 |
| PheGenI | rs5030862 |
| nextbio | rs5030862 |
| hapmap | rs5030862 |
| 1000 genomes | rs5030862 |
| hgdp | rs5030862 |
| ensembl | rs5030862 |
| gopubmed | rs5030862 |
| geneview | rs5030862 |
| scholar | rs5030862 |
| rs5030862 | |
| pharmgkb | rs5030862 |
| gwascentral | rs5030862 |
| openSNP | rs5030862 |
| 23andMe | rs5030862 |
| 23andMe all | rs5030862 |
| SNP Nexus | |
| SNPshot | rs5030862 |
| SNPdbe | rs5030862 |
| MSV3d | rs5030862 |
| Gene | CYP2D6 |
| Chromosome | 22 |
| Orientation | minus |
| Position | 42526670 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | CYP2D6*12 homozygote | |
| (A;G) | carrier of one CYP2D6*12 allele | |
| (G;G) | 0 | normal |
The rs5030862(A) allele defines the CYP2D6*12 variant, which is inactive.