Rs9332239

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is asnp
is mentioned by
dbSNPrs9332239
hapmaprs9332239
hgdprs9332239
ensemblrs9332239
gopubmedrs9332239
scholarrs9332239
googlers9332239
pharmgkbrs9332239
hgvbaseg2prs9332239
medrefsnprs9332239
23andMers9332239
SNP Nexus

Chromosome10
Orientationplus
Position96738766
GenotypeEffect
rs9332239(C;C)CYP2C9*12 homozygote
rs9332239(C;T)carrier of one CYP2C9*12 allele
rs9332239(T;T)normal


Genotypes Magnitude Summary
Rs9332239(C;C) 00 CYP2C9*12 homozygote
Rs9332239(C;T) carrier of one CYP2C9*12 allele
Rs9332239(T;T) normal
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.

? (C;C)