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Genetic Variants associated with Severity of Coronary Artery Disease and Use Thereof

机译:与冠状动脉疾病严重程度有关的遗传变异及其用途

摘要

The present invention relates to a method for providing single nucleotide polymorphism information associated with the severity of coronary artery disease. More specifically, TRPS1 single nucleotide polymorphism rs231150 and CPNE4 gene single nucleotide polymorphisms associated with pathologic features or severity of coronary artery disease (GWAS) to a kit comprising a single nucleotide polymorphic site associated with the severity of coronary artery disease in a population consisting of rs125006. The kits comprising a single nucleotide polymorphic site associated with the severity of coronary artery disease according to the present invention can be used to diagnose or predict the severity of coronary artery disease and provide genetic information related to coronary artery disease , Predictive medicine can be realized.
机译:本发明涉及提供与冠状动脉疾病的严重程度有关的单核苷酸多态性信息的方法。更具体地说,将 TRPS1 单核苷酸多态性rs231150和 CPNE4 基因单核苷酸多态性与冠状动脉疾病(GWAS)的病理特征或严重程度相关联,以试剂盒的形式包含单核苷酸多态性位点与rs125006组成的人群中冠状动脉疾病的严重程度相关。根据本发明的包含与冠状动脉疾病的严重程度相关的单核苷酸多态性位点的试剂盒可用于诊断或预测冠状动脉疾病的严重程度并提供与冠状动脉疾病有关的遗传信息。可以实现预测医学。

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