To provide a method for identifying an individual having an altered risk for developing an acute coronary event or a method for evaluating an individual's likelihood of responding to statin treatment.
The method for identifying an individual having an altered risk of developing an acute coronary event or a method for evaluating an individual's likelihood of responding to statin treatment, comprises a step of detecting the presence or absence of one or more alleles of an SNP in the individual's nucleic acids, wherein the SNP is selected from any one of three specific nucleotide sequences, and the presence or absence of the alleles are correlated with an individual's risk of developing the acute coronary event or likelihood of responding to statin treatment.
DEVLIN JAMES J
WO2005056837A2 | 2005-06-23 |
JPN6012006261; 'Submitted SNP(ss) Details: ss23899966, Aug 20 2004 submitted' Database NCBl dbSNP Short Genetic Variations[online], Accessin No.ss23899966 , 20120201
Natsuki Morishita
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