rs12769205
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12769205(A;A) |
| Make rs12769205(A;G) |
| Make rs12769205(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94775367 |
| Gene | CYP2C19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12769205 |
| dbSNP (classic) | rs12769205 |
| ClinGen | rs12769205 |
| ebi | rs12769205 |
| HLI | rs12769205 |
| Exac | rs12769205 |
| Gnomad | rs12769205 |
| Varsome | rs12769205 |
| LitVar | rs12769205 |
| Map | rs12769205 |
| PheGenI | rs12769205 |
| Biobank | rs12769205 |
| 1000 genomes | rs12769205 |
| hgdp | rs12769205 |
| ensembl | rs12769205 |
| geneview | rs12769205 |
| scholar | rs12769205 |
| rs12769205 | |
| pharmgkb | rs12769205 |
| gwascentral | rs12769205 |
| openSNP | rs12769205 |
| 23andMe | rs12769205 |
| SNPshot | rs12769205 |
| SNPdbe | rs12769205 |
| MSV3d | rs12769205 |
| GWAS Ctlg | rs12769205 |
| Max Magnitude | 0 |
[PMID 26021325
] The CYP2C19 Intron 2 Branch Point SNP is the Ancestral Polymorphism Contributing to the Poor Metabolizer Phenotype in Livers with CYP2C19*35 and CYP2C19*2 Alleles
