Rs1058164
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1058164 |
| PheGenI | rs1058164 |
| nextbio | rs1058164 |
| hapmap | rs1058164 |
| 1000 genomes | rs1058164 |
| hgdp | rs1058164 |
| ensembl | rs1058164 |
| gopubmed | rs1058164 |
| geneview | rs1058164 |
| scholar | rs1058164 |
| rs1058164 | |
| pharmgkb | rs1058164 |
| gwascentral | rs1058164 |
| openSNP | rs1058164 |
| 23andMe | rs1058164 |
| 23andMe all | rs1058164 |
| SNP Nexus | |
| SNPshot | rs1058164 |
| SNPdbe | rs1058164 |
| MSV3d | rs1058164 |
| Gene | CYP2D6 |
| Chromosome | 22 |
| Orientation | minus |
| GMAF | 0.3906 |
| Position | 42525132 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs1058164(C;C) |
| Make rs1058164(C;G) |
| Make rs1058164(G;G) |
The 1661G>C variation in CYP2D6. Involved in a number of decreased and non-functioning CYP2D6 variants. This SNP does not yet appear to be common in consumer tests.
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
