Have questions? Visit https://www.reddit.com/r/SNPedia

rs4987161

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) CYP3A4*17 homozygote
(C;T) carrier of one CYP3A4*17 allele
(T;T) 0 normal
ReferenceGRCh38 38.1/141
Chromosome7
Position99768458
GeneCYP3A4
is asnp
is mentioned by
dbSNPrs4987161
ebirs4987161
HLIrs4987161
Exacrs4987161
Varsomers4987161
Maprs4987161
PheGenIrs4987161
hapmaprs4987161
1000 genomesrs4987161
hgdprs4987161
ensemblrs4987161
gopubmedrs4987161
geneviewrs4987161
scholarrs4987161
googlers4987161
pharmgkbrs4987161
gwascentralrs4987161
openSNPrs4987161
23andMers4987161
23andMe allrs4987161
SNP Nexus

SNPshotrs4987161
SNPdbers4987161
MSV3drs4987161
GWAS Ctlgrs4987161
Max Magnitude0
? (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 23130019OA-icon.png] Frequencies of 23 functionally significant variant alleles related with metabolism of antineoplastic drugs in the chilean population: comparison with caucasian and asian populations.