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rs4986913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP3A4*19 allele
(T;T) CYP3A4*19 homozygote
ReferenceGRCh38 38.1/142
Chromosome7
Position99760836
GeneCYP3A4
is asnp
is mentioned by
dbSNPrs4986913
ebirs4986913
HLIrs4986913
Exacrs4986913
Varsomers4986913
Maprs4986913
PheGenIrs4986913
hapmaprs4986913
1000 genomesrs4986913
hgdprs4986913
ensemblrs4986913
gopubmedrs4986913
geneviewrs4986913
scholarrs4986913
googlers4986913
pharmgkbrs4986913
gwascentralrs4986913
openSNPrs4986913
23andMers4986913
23andMe allrs4986913
SNP Nexus

SNPshotrs4986913
SNPdbers4986913
MSV3drs4986913
GWAS Ctlgrs4986913
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs4986913, also known as 1399C>T, 23237C>T or P467S, is a SNP in the CYP3A4 gene.

The rs4986913(T) allele defines the CYP3A4*19 variant.