Rs28371685
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs28371685 |
| hapmap | rs28371685 |
| hgdp | rs28371685 |
| ensembl | rs28371685 |
| gopubmed | rs28371685 |
| scholar | rs28371685 |
| rs28371685 | |
| pharmgkb | rs28371685 |
| hgvbaseg2p | rs28371685 |
| medrefsnp | rs28371685 |
| 23andMe | rs28371685 |
| SNP Nexus |
| Chromosome | 10 |
| Orientation | plus |
| Position | 96730970 |
| Genotype | Effect |
|---|---|
| rs28371685(C;C) | CYP2C9*11 homozygote |
| rs28371685(C;T) | carrier of one CYP2C9*11 allele |
| rs28371685(T;T) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs28371685(C;C) | 00 | CYP2C9*11 homozygote |
| Rs28371685(C;T) | carrier of one CYP2C9*11 allele | |
| Rs28371685(T;T) | normal |
The rs28371685(T) allele defines the CYP2C9*11 variant, which has decreased activity.
According to a 23andMe discussion This is one of the SNPs which were re-analyzed April 2009. Customers with older data may wish to redownload. SNPs effected rs4420638, rs34276300, rs3091244, rs34601266, rs2033003, rs7900194, rs9332239, rs28371685, rs1229984, and rs28399504.
