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Updated: Jul 20, 2025

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
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A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene

Published on: April 1, 2019

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单核酸多态性 rs2383206对沙特人口冠状动脉疾病风险的影响:一个病例控制研究

N M Bogari1, R M Allam, A Dannoun

  • 1Department of Medical Genetics, Faculty of Medicine, Umm Al-Qura University, Makkah, Saudi Arabia. dr_samar11@yahoo.com.

European review for medical and pharmacological sciences
|July 31, 2023
PubMed
概括

染色体9p21.3上的rs2383206基因变异与患冠状动脉疾病 (CAD) 的风险增加有关. 这一遗传因素,特别是GG基因型,增加了沙特人口的易感性.

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Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Genome-wide Association Studies-GWAS01:11

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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