Rs7900194

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is asnp
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dbSNPrs7900194
hapmaprs7900194
hgdprs7900194
ensemblrs7900194
gopubmedrs7900194
scholarrs7900194
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pharmgkbrs7900194
hgvbaseg2prs7900194
medrefsnprs7900194
23andMers7900194
SNP Nexus

Chromosome10
Orientationplus
Position96692055
GenotypeEffect
rs7900194(A;A)CYP2C9*8 homozygote
rs7900194(A;G)carrier of one CYP2C9*8 allele
rs7900194(G;G)normal


Genotypes Magnitude Summary
Rs7900194(A;A) CYP2C9*8 homozygote
Rs7900194(A;G) carrier of one CYP2C9*8 allele
Rs7900194(G;G) 00 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.