With the help of the given pedigree, find out the probability for the birth of a child having no disease and being a carrier (has the disease mutation in one allele of the gene) in F3 generation.
1/8
Zero
1/4
1/2
To determine the probability of a child being a carrier in the F3 generation, we analyze the transmission of a recessive gene (e.g., autosomal recessive or sex-linked recessive like Haemophilia or Colour Blindness ).
Assuming a standard pedigree scenario where a carrier parent in the F1 generation passes the allele to the F2 generation, who then passes it to F3:
Thus, there is a 1/4 chance for the birth of a carrier child in the F3 generation.
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