Ontology highlight
ABSTRACT: Aim
We conducted a genome-wide association study using the Illumina Exome Array to identify coding SNPs that may explain additional warfarin dose variability.Patients & methods
Analysis was performed after adjustment for clinical variables and genetic factors known to influence warfarin dose among 1680 warfarin users (838 European-Americans and 842 African-Americans). Replication was performed in an independent sample.Results
We confirmed the influence of known genetic variants on warfarin dose variability. Our study is the first to show the association between rs12772169 and warfarin dose in African-Americans. In addition, genes COX15 and FGF5 showed significant association in European-Americans.Conclusion
We identified some novel genes/SNPs that underpin w
SUBMITTER: Liu N
PROVIDER: S-EPMC5619051 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature