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Simplyforensic > Glossary Terms > Single Nucleotide Polymorphisms

Single Nucleotide Polymorphisms

Simplyforensic
Last updated: July 2, 2021 2:18 pm
By Simplyforensic
Published: July 2, 2021
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A single nucleotide polymorphism, or SNP (pronounced “snip”), is a variation at a single position in a DNADNA, or Deoxyribonucleic Acid, is the genetic material found in cells, composed of a double helix structure. It serves as the genetic blueprint for all living organisms. More sequence among individuals. Recall that the DNA sequence is formed from a chain of four nucleotide bases: A, C, G, and T. If more than 1% of a population does not carry the same nucleotide at a specific position in the DNA sequence, then this variation can be classified as a SNP. If a SNP occurs within a gene, then the gene is described as having more than one allele. In these cases, SNPs may lead to variations in the amino acid sequence. SNPs, however, are not just associated with genes; they can also occur in noncoding regions of DNA.

Although a particular SNP may not cause a disorder, some SNPs are associated with certain diseases. These associations allow scientists to look for SNPs in order to evaluate an individual’s genetic predisposition to develop a disease. In addition, if certain SNPs are known to be associated with a trait, then scientists may examine stretches of DNA near these SNPs in an attempt to identify the gene or genes responsible for the trait.

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Forensic Analyst by Profession. With Simplyforensic.com striving to provide a one-stop-all-in-one platform with accessible, reliable, and media-rich content related to forensic science. Education background in B.Sc.Biotechnology and Master of Science in forensic science.
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