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

rs17884712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) CYP2C19*9 homozygote
(A;G) carrier of one CYP2C19*9 allele
(G;G) 0 normal
ReferenceGRCh38 38.1/142
Chromosome10
Position94775489
GeneCYP2C19
is asnp
is mentioned by
dbSNPrs17884712
ebirs17884712
HLIrs17884712
Exacrs17884712
Varsomers17884712
Maprs17884712
PheGenIrs17884712
hapmaprs17884712
1000 genomesrs17884712
hgdprs17884712
ensemblrs17884712
gopubmedrs17884712
geneviewrs17884712
scholarrs17884712
googlers17884712
pharmgkbrs17884712
gwascentralrs17884712
openSNPrs17884712
23andMers17884712
23andMe allrs17884712
SNP Nexus

SNPshotrs17884712
SNPdbers17884712
MSV3drs17884712
GWAS Ctlgrs17884712
GMAF0.003214
Max Magnitude0
The rs17884712(A) allele defines the CYP2C19 variant known as CYP2C19*9, which is associated with a slight decrease in the metabolism of S-mephenytoin (at least in vitro).[PMID 12464799]