Related Experiment Video
Updated: May 13, 2025

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
Founder Variants in the Mexican Population: A Systematic Review
Sylvia Harari-Arakindji1, Teresa Metta-Harari1, Isabel Espino-Gutiérrez2
1Facultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Mexico City, Mexico.
This study identifies 21 founder variants (FVs) in 19 genes linked to diseases in the Mexican population. Some frequent variants may have European origins, offering insights into genetic history and health.
Area of Science:
- Population Genetics
- Medical Genetics
- Genomic Medicine
Background:
- Founder variants (FVs) are common in homogeneous populations and impact genetic disorder prevalence.
- Comprehensive descriptions of FVs in the Mexican population are lacking.
- Understanding FVs is crucial for characterizing the genetic landscape of specific populations.
Conclusions:
- This review offers a comprehensive overview of FVs in the Mexican population, enhancing understanding of regional genetic architecture.
- The findings provide a framework for exploring links between FVs and clinical, historical, and cultural factors.
- Further research can leverage this data to investigate disease etiology and population history in Mexico.
More Related Videos
11:35Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay EMSA and DNA-affinity Precipitation Assay DAPA
Published on: August 21, 2016
09:34Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Related Concept Videos
Pleiotropy
Incomplete Dominance
Multiple Allele Traits
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Mutation, Gene Flow, and Genetic Drift
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...