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rs12721627

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 normal
(C;G) carrier of one CYP3A4*16 allele
(G;G) CYP3A4*16 homozygote
ReferenceGRCh38 38.1/141
Chromosome7
Position99768470
GeneCYP3A4
is asnp
is mentioned by
dbSNPrs12721627
ebirs12721627
HLIrs12721627
Exacrs12721627
Varsomers12721627
Maprs12721627
PheGenIrs12721627
hapmaprs12721627
1000 genomesrs12721627
hgdprs12721627
ensemblrs12721627
gopubmedrs12721627
geneviewrs12721627
scholarrs12721627
googlers12721627
pharmgkbrs12721627
gwascentralrs12721627
openSNPrs12721627
23andMers12721627
23andMe allrs12721627
SNP Nexus

SNPshotrs12721627
SNPdbers12721627
MSV3drs12721627
GWAS Ctlgrs12721627
GMAF0.001377
Max Magnitude0
rs12721627, also known as 554C>G, 15603C>G or T185S, is a SNP in the CYP3A4 gene.

The rs12721627(G) allele defines the CYP3A4*16 variant.





[PMID 20082485OA-icon.png] Genetic variants involved in gallstone formation and capsaicin metabolism, and the risk of gallbladder cancer in Chilean women.