Rs2069526
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2069526 |
| PheGenI | rs2069526 |
| nextbio | rs2069526 |
| hapmap | rs2069526 |
| 1000 genomes | rs2069526 |
| hgdp | rs2069526 |
| ensembl | rs2069526 |
| gopubmed | rs2069526 |
| geneview | rs2069526 |
| scholar | rs2069526 |
| rs2069526 | |
| pharmgkb | rs2069526 |
| gwascentral | rs2069526 |
| openSNP | rs2069526 |
| 23andMe | rs2069526 |
| 23andMe all | rs2069526 |
| SNP Nexus | |
| SNPshot | rs2069526 |
| SNPdbe | rs2069526 |
| MSV3d | rs2069526 |
| Gene | CYP1A2 |
| Chromosome | 15 |
| Orientation | plus |
| GMAF | 0.0636 |
| Position | 75041341 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | CYP1A2*1K_-739T>G homozygote | |
| (G;T) | carrier of one CYP1A2*1K_-739T>G allele | |
| (T;T) | 0 | normal |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
The rs2069526(T) allele defines the CYP1A2*1K_-739T>G variant.
| GET Evidence | |
|---|---|
| rs2069526 | |
| aa_change | |
| aa_change_short | |
| impact | pharmacogenetic |
| qualified_impact | Insufficiently evaluated pharmacogenetic |
| overall_frequency | 0.0625 |
| summary | |
