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发明公开
CN101768630A 人肾素结合蛋白基因的SNP位点及其检测方法和诊断用途 无效 - 撤回

人肾素结合蛋白基因的SNP位点及其检测方法和诊断用途
摘要：
本发明公开了人肾素结合蛋白基因启动子区存在的一个SNP位点，是人肾素结合蛋白基因启动子区-1590位的A/G多态，具有SEQ？ID？NO.1所示的核苷酸序列。此外，本发明还公开了检测人肾素结合蛋白基因SNP位点的方法及其检测引物。另外，本发明还公开了人肾素结合蛋白基因的SNP位点在诊断冠心病中的用途。
摘要（英）：

The invention discloses an SNP locus in a human rennin binding protein gene promoter region, which is A/G polymorphism of a human rennin binding protein gene promoter region-1,590 locus and has a nucleotide sequence expressed as SEQ ID No.1. Moreover, the invention also discloses a method for detecting the SNP locus of the human rennin binding protein gene and a detection primer. In addition, the invention also discloses application of the SNP locus of the human rennin binding protein gene in diagnosing coronary disease.

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