Influence of common and rare genetic variation on warfarin dose among African–Americans and European–Americans using the exome array
Author(s) -
Nianjun Liu,
Marguerite R. Irvin,
Degui Zhi,
Amit Patki,
T. Mark Beasley,
Deborah A. Nickerson,
Charles E. Hill,
Jinbo Chen,
Stephen E. Kimmel,
Nita A. Limdi
Publication year - 2017
Publication title -
pharmacogenomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.541
H-Index - 91
eISSN - 1744-8042
pISSN - 1462-2416
DOI - 10.2217/pgs-2017-0046
Subject(s) - warfarin , single nucleotide polymorphism , vkorc1 , exome , exome sequencing , genome wide association study , genetic variation , biology , genetic association , genetics , medicine , gene , pharmacogenetics , mutation , genotype , atrial fibrillation
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 warfarin dose response. Further replication is needed to confirm our findings.
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