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Rs7900194

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Orientationplus
is asnp
is mentioned by
dbSNPrs7900194
PheGenIrs7900194
hapmaprs7900194
1000 genomesrs7900194
hgdprs7900194
ensemblrs7900194
gopubmedrs7900194
geneviewrs7900194
scholarrs7900194
googlers7900194
pharmgkbrs7900194
gwascentralrs7900194
openSNPrs7900194
23andMers7900194
23andMe allrs7900194
SNP Nexus

SNPshotrs7900194
SNPdbers7900194
MSV3drs7900194
GeneCYP2C9
Chromosome10
Orientationplus
GMAF0.0124
Position96702066
ReferenceGRCh37 37.1/131
Max Magnitude0
Geno Mag Summary
(A;A) CYP2C9*8 homozygote
(A;G) carrier of one CYP2C9*8 allele
(G;G) 0 normal

rs7900194, also known as 449G>A, 3627G>A or R150H, is a SNP in the CYP2C9 gene.

The rs7900194(A) allele defines the CYP2C9*8 variant, which has decreased activity.

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 19663669OA-icon.png] CYP2C9*8 is prevalent among African-Americans: implications for pharmacogenetic dosing.


GET Evidence
CYP2C9-R150H
aa_change Arg150His
aa_change_short R150H
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0202715
summary