rs17884712
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | CYP2C19*9 homozygote | |
| (A;G) | carrier of one CYP2C19*9 allele | |
| (G;G) | 0 | normal |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94775489 |
| Gene | CYP2C19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17884712 |
| dbSNP (classic) | rs17884712 |
| ClinGen | rs17884712 |
| ebi | rs17884712 |
| HLI | rs17884712 |
| Exac | rs17884712 |
| Gnomad | rs17884712 |
| Varsome | rs17884712 |
| LitVar | rs17884712 |
| Map | rs17884712 |
| PheGenI | rs17884712 |
| Biobank | rs17884712 |
| 1000 genomes | rs17884712 |
| hgdp | rs17884712 |
| ensembl | rs17884712 |
| geneview | rs17884712 |
| scholar | rs17884712 |
| rs17884712 | |
| pharmgkb | rs17884712 |
| gwascentral | rs17884712 |
| openSNP | rs17884712 |
| 23andMe | rs17884712 |
| SNPshot | rs17884712 |
| SNPdbe | rs17884712 |
| MSV3d | rs17884712 |
| GWAS Ctlg | rs17884712 |
| GMAF | 0.003214 |
| Max Magnitude | 0 |
The rs17884712(A) allele defines the CYP2C19 variant known as CYP2C19*9, which is associated with a slight decrease in the metabolism of S-mephenytoin (at least in vitro).[PMID 12464799]
