Learning Objectives
- Master the Hardy-Weinberg equations for allele and genotype frequencies.
- Identify the five essential assumptions for equilibrium.
- Calculate carrier frequency (2pq) given disease prevalence (
).
- Distinguish between autosomal and X-linked frequency calculations.
1. The Fundamental Equations
In a stable population with random mating, allele frequencies remain constant. We use two primary equations:
- Allele Frequency:
= frequency of dominant allele (A)
= frequency of recessive allele (a)
- Genotype Frequency:
= frequency of homozygous dominant (AA)
= frequency of homozygous recessive (aa/disease prevalence)
- $Latex2pq$ = frequency of heterozygotes (carrier frequency)
Activity
2. Hardy-Weinberg Assumptions
For a population to stay in equilibrium (where $p$ and $q$ do not change), five “No” rules must apply:
| Requirement | Meaning |
|---|---|
| No Mutation | The alleles themselves do not change. |
| No Selection | Natural selection does not favor one genotype over another. |
| Random Mating | No consanguinity or mate choice based on the trait. |
| No Migration | No gene flow in or out of the population. |
| Large Population | Prevents genetic drift from altering frequencies. |
Activity
3. Clinical Calculations (High-Yield)
Autosomal Recessive (e.g., Cystic Fibrosis)
For rare diseases, we assume $p \approx 1$. Therefore, the carrier frequency $2pq \approx 2q$.
- If prevalence (
) = 1/3200
- Then
(1.7%)
- Carrier frequency (
)
(3.4%)
X-Linked Recessive
The frequency in males equals (because they only have one X chromosome). The frequency in females equals
.
Activity
