Conclusions:（1） CYP1A1 Msp1 single nucleotide polymorphisms possibly was a genetic risk factor in the incidence of COPD.
结论1、CYP1A1 Msp1基因多态性可能是COPD发病的危险因素。
参考来源 - CYP1A1及ILMoreover, Many pathogenic and genetic diseases are associated with changes in the sequence of particular genes. Among these changes, the point mutation, i. e. single nucleotide polymorphisms (SNPs), are the most abundant form of genetic variation.
此外,人类的许多遗传性疾病都是由于基因的变异引起的,其中尤以单碱基的突变,即单碱基多态性最为普遍。
参考来源 - 基于纳米粒子、酶的信号放大生物分析方法研究·2,447,543篇论文数据，部分数据来源于NoteExpress
Scientists later refined the map by looking for single variations called SNPs or single nucleotide polymorphisms.
科学家们稍后通过利用称为SNP的单核苷酸多态性使遗传图谱更加精细。
Current genetic tests analyze about 600,000 SNPs (single nucleotide polymorphisms) or 0.1 percent of the entire genome.
当前的基因检测分析了大约600,000个SNP(单核苷酸多态性)，只是整个基因组的千分之一。
Each person's collection of these changes (called "single nucleotide polymorphisms, or SNPs) contributes to his or her individuality.
每个人带有的这些差异的集合（称作单核苷酸多态性，简称SNPs）造成了他/她的独特性。
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