rs12721629
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal |
| (C;T) | carrier of one CYP3A4*12 allele | |
| (T;T) | 2.5 | CYP3A4*12 homozygote |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 99762177 |
| Gene | CYP3A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12721629 |
| dbSNP (classic) | rs12721629 |
| ClinGen | rs12721629 |
| ebi | rs12721629 |
| HLI | rs12721629 |
| Exac | rs12721629 |
| Gnomad | rs12721629 |
| Varsome | rs12721629 |
| LitVar | rs12721629 |
| Map | rs12721629 |
| PheGenI | rs12721629 |
| Biobank | rs12721629 |
| 1000 genomes | rs12721629 |
| hgdp | rs12721629 |
| ensembl | rs12721629 |
| geneview | rs12721629 |
| scholar | rs12721629 |
| rs12721629 | |
| pharmgkb | rs12721629 |
| gwascentral | rs12721629 |
| openSNP | rs12721629 |
| 23andMe | rs12721629 |
| SNPshot | rs12721629 |
| SNPdbe | rs12721629 |
| MSV3d | rs12721629 |
| GWAS Ctlg | rs12721629 |
| Merged from | Rs45614732 |
| GMAF | 0.002755 |
| Max Magnitude | 2.5 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs12721629, also known as 1117C>T, 21896C>T or L373F, is a SNP in the CYP3A4 gene.
The rs12721629(T) allele defines the CYP3A4*12 variant.
This SNP includes a SNP formerly known as rs45614732 that has now been merged into it.
