首页> 外国专利> Method for diagnosing premature ovarian failure comprising genotype analysis or haplotype analysis of 2 single nucleotide polymorphisms

Method for diagnosing premature ovarian failure comprising genotype analysis or haplotype analysis of 2 single nucleotide polymorphisms

机译:诊断卵巢早衰的方法,包括2个单核苷酸多态性的基因型分析或单倍型分析

摘要

PURPOSE: A method for diagnosing premature menopause is provided to obtain information for diagnosis. CONSTITUTION: A method for analyzing SNPs in a test sample comprises: a step of preparing nucleic acid from the sample; and a step of analyzing genotype of two kinds of SNPs selected from polynucleotides having DNA sequences of sequence numbers 1-5. The SNPs include 301th base in a DNA sequence of sequence number 1, 565th base in a DNA sequence of sequence number 2, 301th base in a DNA sequence of sequence number 3, 301th base in a DNA sequence of sequence number 4, and 301th base in a DNA sequence of sequence number 5.
机译:目的:提供了一种诊断更年期更早的方法,以获取诊断信息。构成:一种分析测试样品中单核苷酸多态性的方法,包括:从样品中制备核酸的步骤;分析选自具有序列号1-5的DNA序列的多核苷酸的两种SNP的基因型的步骤。 SNP在序列号1的DNA序列中包含第301个碱基,在序列号2的DNA序列中包含第565个碱基,在序列号3的DNA序列中包含第301个碱基,在序列号4的DNA序列中包含第301个碱基,在序列号5的DNA序列中。

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