Rs2017319
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2017319 |
| PheGenI | rs2017319 |
| nextbio | rs2017319 |
| hapmap | rs2017319 |
| 1000 genomes | rs2017319 |
| hgdp | rs2017319 |
| ensembl | rs2017319 |
| gopubmed | rs2017319 |
| geneview | rs2017319 |
| scholar | rs2017319 |
| rs2017319 | |
| pharmgkb | rs2017319 |
| gwascentral | rs2017319 |
| openSNP | rs2017319 |
| 23andMe | rs2017319 |
| 23andMe all | rs2017319 |
| SNP Nexus | |
| SNPshot | rs2017319 |
| SNPdbe | rs2017319 |
| MSV3d | rs2017319 |
| Gene | CYP2C9 |
| Chromosome | 10 |
| Orientation | plus |
| GMAF | 0.0252 |
| Position | 96748635 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal |
| (C;T) | carrier of one CYP2C9_50196C>T allele | |
| (T;T) | CYP2C9_50196C>T homozygote |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
The rs2017319(T) allele defines the CYP2C9_50196C>T variant, about which little is known.
[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.
