Single-nucleotide polymorphism: Difference between revisions
CSV import |
CSV import |
||
| Line 45: | Line 45: | ||
{{Genetics-stub}} | {{Genetics-stub}} | ||
<gallery> | |||
File:dna-SNP.svg|Single-nucleotide polymorphism | |||
File:Types_of_SNP_new1.png|Types of SNP | |||
File:Associations_between_SNPs,_methylation_patterns_and_gene_expression.png|Associations between SNPs, methylation patterns, and gene expression | |||
</gallery> | |||
Latest revision as of 04:08, 18 February 2025
Single-nucleotide polymorphism (SNP; pronounced "snip") is a variation in a single nucleotide that occurs at a specific position in the genome. SNPs are the most common type of genetic variation among people. Each SNP represents a difference in a single DNA building block, called a nucleotide. For example, a SNP may replace the nucleotide cytosine (C) with the nucleotide thymine (T) in a certain stretch of DNA. SNPs can occur within coding regions of genes, non-coding regions of genes, or in the intergenic regions between genes. Depending on where they occur, SNPs can have a wide range of effects on gene function and health.
Types of SNPs[edit]
There are several types of SNPs, including:
- Synonymous SNPs: These do not change the protein sequence that the gene produces.
- Non-synonymous SNPs: These change the amino acid sequence of a protein and can affect the protein's function.
- Insertion/deletion SNPs: These involve the insertion or deletion of nucleotides in the genome.
- Regulatory SNPs: These occur in gene regulatory regions and can affect gene expression.
Importance of SNPs[edit]
SNPs are important for several reasons:
- Genetic Diversity: They contribute to the genetic diversity among individuals, which can influence a wide range of physical traits and susceptibility to diseases.
- Disease Research: SNPs are used in genetic association studies to identify genes that may contribute to common diseases.
- Pharmacogenomics: SNPs can influence how individuals respond to drugs, which is the basis of pharmacogenomics.
- Forensic Science: SNPs can be used in forensic testing to help identify individuals.
Detecting SNPs[edit]
SNPs can be detected using various molecular biology techniques, including:
Applications of SNP Information[edit]
The information gained from studying SNPs has a wide range of applications, including:
- Understanding the genetic basis of diseases
- Developing new drugs and treatments
- Personalized medicine, where treatments are tailored to an individual's genetic makeup
- Improving crop varieties in agriculture
Challenges and Considerations[edit]
While SNPs offer great potential for advancing medical and biological research, there are challenges and considerations, including:
- The need for large-scale studies to accurately identify SNP-disease associations
- Ethical considerations in genetic testing and privacy
- The potential for genetic discrimination based on SNP information
See Also[edit]
-
Single-nucleotide polymorphism
-
Types of SNP
-
Associations between SNPs, methylation patterns, and gene expression
