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rs4986907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) CYP3A4*15A homozygote
(A;G) carrier of one CYP3A4*15A allele
(G;G) 0 normal
ReferenceGRCh38 38.1/142
Chromosome7
Position99769804
GeneCYP3A4
is asnp
is mentioned by
dbSNPrs4986907
ebirs4986907
HLIrs4986907
Exacrs4986907
Varsomers4986907
Maprs4986907
PheGenIrs4986907
hapmaprs4986907
1000 genomesrs4986907
hgdprs4986907
ensemblrs4986907
gopubmedrs4986907
geneviewrs4986907
scholarrs4986907
googlers4986907
pharmgkbrs4986907
gwascentralrs4986907
openSNPrs4986907
23andMers4986907
23andMe allrs4986907
SNP Nexus

SNPshotrs4986907
SNPdbers4986907
MSV3drs4986907
GWAS Ctlgrs4986907
GMAF0.004132
Max Magnitude0
? (A;A) (A;G) (G;G) 28
rs4986907, also known as 485G>A, 14269G>A or R162Q, is a SNP in the CYP3A4 gene.

The rs4986907(A) allele defines the CYP3A4*15A variant.



[PMID 17615053OA-icon.png] Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.