However, an allele's frequency within a population can vary greatly. For instance, Caucasians have an allele frequency of 0.025 for the mutant cystic fibrosis allele and 0.975 for the normal allele. This has an impact on how alleles are distributed across a population as a whole.
A fatal hereditary condition that harms the lungs and digestive system.
The cells that make mucus, perspiration, and digestive fluids are impacted by cystic fibrosis. These fluids start to thicken and cling together as a result. They then block off the passages, ducts, and tubes.
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