Hardy-Weinberg Calculations

20 questions β€’ 1 test β€’ tap a section to begin

Welcome! 6.2 Hardy-Weinberg Calculations β€” Test 1 — 20 questions, CSIR-NET style.

What this test covers

  • Allele & genotype frequency calculations
  • Carrier frequency in recessive disorders
  • X-linked allele frequencies
  • Counting alleles from genotype data

How to use

  • Tap the test below — it opens on its own full screen. Use ← All tests at the top to come back.
  • Each question has a 40-second timer. Answer, then Submit to see your score.
  • Tap πŸ“‹ View Solution under any question for a full explanation.

Open Review at the bottom for a quick revision list of every question with its correct answer.

Quiz
Question Palette
Quiz
Question Palette
Quiz
Explanation:

Quick revision: every question with its correct answer. For the full explanation, open the test and tap View Solution.

6.2 Hardy-Weinberg Calculations β€” Test 1
Q1. In a population at HWE, the dominant-allele frequency is 0.6. The frequency of heterozygous individuals is:βœ“ 0.48
Q2. In a random sample of 400 individuals at HWE, 36 are homozygous recessive (aa). How many are expected to carry at least one dominant allele A?βœ“ 364
Q3. A large random-mating population has 4% recessive (affected) individuals. The expected carrier frequency is:βœ“ 32%
Q4. In a population of 500 diploid individuals, 400 T alleles are counted at a locus. The number of t alleles present is:βœ“ 600
Q5. A population of 2000 plants has 100 rr (white), 800 Rr (pink) and 1100 RR (red). The frequency of the r allele is:βœ“ 0.25
Q6. In a sample of 110 individuals (65 BB, 30 Bb, 15 bb), the frequency of the b allele is:βœ“ 0.27
Q7. In a population of 1000 individuals (600 MM, 300 MN, 100 NN), the frequencies of M and N are:βœ“ M 0.75, N 0.25
Q8. In a population of 1000 dogs (360 BB, 480 Bb, 160 bb), the frequency of the b allele is:βœ“ 0.4
Q9. MN blood-type counts are 1787 M, 3039 MN and 1303 N (total 6129). The frequency of the L^N allele is approximately:βœ“ 0.4605
Q10. At HWE, the genotype frequencies are f(A1A1) = 0.59, f(A1A2) = 0.16, f(A2A2) = 0.25. The allele frequencies are:βœ“ A1 = 0.67, A2 = 0.33
Q11. At HWE, the frequency of one homozygous genotype is 0.64. The heterozygote frequency is:βœ“ 0.32
Q12. At HWE, the total frequency of homozygotes is 0.68. The two allele frequencies are:βœ“ 0.2 and 0.8
Q13. At HWE, a two-allele locus has a heterozygote frequency of 0.32. The frequency of the rarer allele is:βœ“ 0.2
Q14. In a random-mating population, allele Y has frequency 0.70. The frequency of Y/y heterozygotes is:βœ“ 0.42
Q15. An autosomal recessive disorder at HWE has an incidence of 1 in 6400. The approximate carrier frequency is:βœ“ 1 in 40
Q16. An autosomal recessive condition affects 1 in 10,000 newborns. The expected carrier frequency is approximately:βœ“ 1 in 50
Q17. In a population where 1 in 400 people has a recessive disorder, the expected proportion of carriers is:βœ“ 38/400
Q18. An X-linked recessive disease has a frequency of 0.16 among females. Its frequency among males is:βœ“ 0.4
Q19. The frequency of males affected by an X-linked recessive disorder is 0.1. The frequency of affected females is:βœ“ 0.01
Q20. Match each scenario with its computed value and select the correct option.βœ“ A-iii, B-i, C-iv, D-ii