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
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
21. Population Genetics
Hardy Weinberg
5:38 minutes
Problem 13
Textbook Question
Textbook QuestionAssume that a recessive autosomal disorder occurs in 1 of 10,000 individuals (0.0001) in the general population and that in this population about 2 percent (0.02) of the individuals are carriers for the disorder. Estimate the probability of this disorder occurring in the offspring of a marriage between first cousins. Compare this probability to the population at large.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Autosomal Recessive Inheritance
Autosomal recessive inheritance refers to a pattern where two copies of a mutated gene (one from each parent) are necessary for an individual to express a recessive disorder. Carriers, who possess one normal and one mutated gene, do not show symptoms but can pass the mutated gene to their offspring. This concept is crucial for understanding how the disorder can manifest in children of parents who are both carriers.
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Autosomal Pedigrees
Carrier Frequency
Carrier frequency is the proportion of individuals in a population who carry one copy of a recessive allele for a genetic disorder. In this case, with a carrier frequency of 2 percent, it indicates that 2 out of every 100 individuals are carriers. This statistic is essential for estimating the likelihood of two carriers mating and having an affected child, especially in consanguineous relationships like first cousins.
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New Alleles and Migration
Inbreeding and Genetic Risk
Inbreeding, or mating between closely related individuals, increases the probability that both parents carry the same recessive allele, thereby raising the risk of offspring inheriting the disorder. In the case of first cousins, the genetic relatedness is higher than that of unrelated individuals, which can significantly elevate the risk of recessive disorders manifesting in their children compared to the general population.
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Descriptive Genetics
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