Table of contents

1. Introduction to Genetics51m
2. Mendel's Laws of Inheritance3h 37m
3. Extensions to Mendelian Inheritance2h 41m
4. Genetic Mapping and Linkage2h 28m
5. Genetics of Bacteria and Viruses1h 21m
6. Chromosomal Variation1h 48m
7. DNA and Chromosome Structure56m
8. DNA Replication1h 10m
9. Mitosis and Meiosis1h 34m
10. Transcription1h 0m
11. Translation58m
12. Gene Regulation in Prokaryotes1h 19m
13. Gene Regulation in Eukaryotes44m
14. Genetic Control of Development44m
15. Genomes and Genomics1h 50m
16. Transposable Elements47m
17. Mutation, Repair, and Recombination1h 6m
18. Molecular Genetic Tools19m
- Genetic Cloning
  9m
- Methods for Analyzing DNA
  9m
19. Cancer Genetics29m
- Overview of Cancer
  21m
- Cancer Mutations
  7m
20. Quantitative Genetics1h 26m
21. Population Genetics50m
- Hardy Weinberg
  19m
- Allelic Frequency Changes
  31m
22. Evolutionary Genetics29m

1. Introduction to Genetics

Modern Genetics

Genetics

1. Introduction to Genetics

Modern Genetics

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Multiple Choice

True or False:
Single nucleotide polymorphisms are common in the human population.

True

False

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Verified step by step guidance

Understand the term 'Single Nucleotide Polymorphisms (SNPs)': SNPs are variations at a single position in a DNA sequence among individuals.

Recognize the prevalence of SNPs: SNPs are the most common type of genetic variation among people.

Consider the frequency of SNPs: In the human genome, SNPs occur approximately once in every 300 nucleotides, which means there are roughly 10 million SNPs in the human genome.

Evaluate the impact of SNPs: While many SNPs have no effect on health or development, some can influence how humans develop diseases and respond to pathogens, chemicals, drugs, vaccines, and other agents.

Conclude based on the information: Given their common occurrence and significant presence in the human genome, the statement that SNPs are common in the human population is true.