Rs5787121
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs5787121 |
| hapmap | rs5787121 |
| hgdp | rs5787121 |
| ensembl | rs5787121 |
| gopubmed | rs5787121 |
| scholar | rs5787121 |
| rs5787121 | |
| pharmgkb | rs5787121 |
| hgvbaseg2p | rs5787121 |
| medrefsnp | rs5787121 |
| 23andMe | rs5787121 |
| SNP Nexus |
| Chromosome | 10 |
| Orientation | plus |
| Position | 96602503 |
| Genotype | Effect |
|---|---|
| rs5787121(-;-) | CYP2C19 G439- homozygote |
| rs5787121(-;G) | carrier of one CYP2C19 G439- allele |
| rs5787121(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs5787121(-;-) | CYP2C19 G439- homozygote | |
| Rs5787121(-;G) | carrier of one CYP2C19 G439- allele | |
| Rs5787121(G;G) | 00 | normal |
The rs5787121(-) (i.e. deletion) SNP defines the CYP2C19 allele known as G439- or 90052delG.