rs4987161
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | CYP3A4*17 homozygote | |
(C;T) | carrier of one CYP3A4*17 allele | |
(T;T) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 99768458 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs4987161 |
dbSNP (classic) | rs4987161 |
ClinGen | rs4987161 |
ebi | rs4987161 |
HLI | rs4987161 |
Exac | rs4987161 |
Gnomad | rs4987161 |
Varsome | rs4987161 |
LitVar | rs4987161 |
Map | rs4987161 |
PheGenI | rs4987161 |
Biobank | rs4987161 |
1000 genomes | rs4987161 |
hgdp | rs4987161 |
ensembl | rs4987161 |
geneview | rs4987161 |
scholar | rs4987161 |
rs4987161 | |
pharmgkb | rs4987161 |
gwascentral | rs4987161 |
openSNP | rs4987161 |
23andMe | rs4987161 |
SNPshot | rs4987161 |
SNPdbe | rs4987161 |
MSV3d | rs4987161 |
GWAS Ctlg | rs4987161 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs4987161, also known as 566T>C, 15615T>C or F189S, is a SNP in the CYP3A4 gene.
The rs4987161(C) allele defines the CYP3A4*17 variant.
[PMID 23130019] Frequencies of 23 functionally significant variant alleles related with metabolism of antineoplastic drugs in the chilean population: comparison with caucasian and asian populations.