Rs9332131

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Warfarin (Coumadin®)
Orientationplus
Geno Mag Summary
(-;-) 2.5 CYP2C9*6 homozygote
(-;A) carrier of one CYP2C9*6 allele
(A;A) 0 normal
ReferenceGRCh37 37.1/131
Chromosome10
Position96709039
GeneCYP2C9
is asnp
is mentioned by
dbSNPrs9332131
Exacrs9332131
PheGenIrs9332131
nextbiors9332131
hapmaprs9332131
1000 genomesrs9332131
hgdprs9332131
ensemblrs9332131
gopubmedrs9332131
geneviewrs9332131
scholarrs9332131
googlers9332131
pharmgkbrs9332131
gwascentralrs9332131
openSNPrs9332131
23andMers9332131
23andMe allrs9332131
SNP Nexus

SNPshotrs9332131
SNPdbers9332131
MSV3drs9332131
Max Magnitude2.5
CPMC Logo.png

This SNP has been recognized by the Coriell Personalized Medicine Collaborative ICOB.
Additional information is available here

rs9332131, also known as 818delA, 10601delA or 273Frame shift, is a SNP in the CYP2C9 gene.

The rs9332131(-) allele defines the CYP2C9*6 variant, which is inactive.


[PMID 20214591] Pharmacogenomics in aspirin intolerance



[PMID 18466099OA-icon.png] Influence of CYP2C9 and VKORC1 on warfarin dose, anticoagulation attainment and maintenance among European-Americans and African-Americans.


[PMID 18752379OA-icon.png] Warfarin pharmacogenetics.


[PMID 19955245OA-icon.png] Warfarin sensitivity genotyping: a review of the literature and summary of patient experience.