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

rs4986909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP3A4*13 allele
(T;T) CYP3A4*13 homozygote
ReferenceGRCh38 38.1/142
Chromosome7
Position99762047
GeneCYP3A4
is asnp
is mentioned by
dbSNPrs4986909
ebirs4986909
HLIrs4986909
Exacrs4986909
Varsomers4986909
Maprs4986909
PheGenIrs4986909
hapmaprs4986909
1000 genomesrs4986909
hgdprs4986909
ensemblrs4986909
gopubmedrs4986909
geneviewrs4986909
scholarrs4986909
googlers4986909
pharmgkbrs4986909
gwascentralrs4986909
openSNPrs4986909
23andMers4986909
23andMe allrs4986909
SNP Nexus

SNPshotrs4986909
SNPdbers4986909
MSV3drs4986909
GWAS Ctlgrs4986909
Max Magnitude0
? (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.