rs4986909
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | normal |
| (C;T) | carrier of one CYP3A4*13 allele | |
| (T;T) | CYP3A4*13 homozygote |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 99762047 |
| Gene | CYP3A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4986909 |
| dbSNP (classic) | rs4986909 |
| ClinGen | rs4986909 |
| ebi | rs4986909 |
| HLI | rs4986909 |
| Exac | rs4986909 |
| Gnomad | rs4986909 |
| Varsome | rs4986909 |
| LitVar | rs4986909 |
| Map | rs4986909 |
| PheGenI | rs4986909 |
| Biobank | rs4986909 |
| 1000 genomes | rs4986909 |
| hgdp | rs4986909 |
| ensembl | rs4986909 |
| geneview | rs4986909 |
| scholar | rs4986909 |
| rs4986909 | |
| pharmgkb | rs4986909 |
| gwascentral | rs4986909 |
| openSNP | rs4986909 |
| 23andMe | rs4986909 |
| SNPshot | rs4986909 |
| SNPdbe | rs4986909 |
| MSV3d | rs4986909 |
| GWAS Ctlg | rs4986909 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
rs4986909, also known as 1247C>T, 22026C>T or P416L, is a SNP in the CYP3A4 gene.
The rs4986909(T) allele defines the CYP3A4*13 variant.
