Rs9332239

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Orientationplus
Geno Mag Summary
(C;C) 0 normal
(C;T) carrier of one CYP2C9*12 allele
(T;T) CYP2C9*12 homozygote
ReferenceGRCh37 37.1/131
Chromosome10
Position96748777
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs9332239
Exacrs9332239
PheGenIrs9332239
nextbiors9332239
hapmaprs9332239
1000 genomesrs9332239
hgdprs9332239
ensemblrs9332239
gopubmedrs9332239
geneviewrs9332239
scholarrs9332239
googlers9332239
pharmgkbrs9332239
gwascentralrs9332239
openSNPrs9332239
23andMers9332239
23andMe allrs9332239
SNP Nexus

SNPshotrs9332239
SNPdbers9332239
MSV3drs9332239
GMAF0.001837
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs9332239, also known as 1465C>T, 50338C>T or P489S, is a SNP in the CYP2C9 gene.

The rs9332239(T) allele defines the CYP2C9*12 variant.

According to a 23andMe discussion This is one of the SNPs which were re-analyzed April 2009. Customers with older data may wish to redownload. SNPs effected rs4420638, rs34276300, rs3091244, rs34601266, rs2033003, rs7900194, rs9332239, rs28371685, rs1229984, and rs28399504.


[PMID 23688605] First report of warfarin dose requirements in patients possessing the CYP2C9*12 allele.