rs72558186
From SNPedia
| Clopidogrel (Plavix®) |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | CYP2C19*7 homozygote | |
| (A;T) | carrier of one CYP2C19*7 allele | |
| (T;T) | 0 | normal |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 94781999 |
| Gene | CYP2C19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72558186 |
| dbSNP (classic) | rs72558186 |
| ClinGen | rs72558186 |
| ebi | rs72558186 |
| HLI | rs72558186 |
| Exac | rs72558186 |
| Gnomad | rs72558186 |
| Varsome | rs72558186 |
| LitVar | rs72558186 |
| Map | rs72558186 |
| PheGenI | rs72558186 |
| Biobank | rs72558186 |
| 1000 genomes | rs72558186 |
| hgdp | rs72558186 |
| ensembl | rs72558186 |
| geneview | rs72558186 |
| scholar | rs72558186 |
| rs72558186 | |
| pharmgkb | rs72558186 |
| gwascentral | rs72558186 |
| openSNP | rs72558186 |
| 23andMe | rs72558186 |
| SNPshot | rs72558186 |
| SNPdbe | rs72558186 |
| MSV3d | rs72558186 |
| GWAS Ctlg | rs72558186 |
| Max Magnitude | 0 |
| This SNP has been recognized by the Coriell Personalized Medicine Collaborative ICOB.
|
The rs72558186(A) SNP represents a CYP2C19 allele known as CYP2C19*7; it reflects a splice donor mutation that leads to a poor metabolizer phenotype.[PMID 10411572]
This SNP is also known as CYP2C19_19294T>A, and in the Affymetrix DMET panel, as DMET3B10072.
Note: absence of allele frequency data leaves this as a possible ambiguous flip.
