Tay-Sachs disease (TSD) is an inborn error of metabolism that results in death by the age of two. It is caused by a mutation in the HEXA gene located on chromosome 15. You are a genetic counselor and one day you interview a phenotypically normal couple. The husband had a female first cousin on his fathers side, who died from TSD. The wife had a maternal uncle, who died from TSD. There are no other known cases in either of the families and none of the matings were/are between related individuals. Assume that this trait is very rare. [Note: a first cousin is a child of ones parents sibling.]Draw a pedigree of the families of this couple, showing the relevant individuals. You will need the pedigree to answer the following questions.(a) What is the probability that the wife is a carrier for TSD?Group of answer choices1/21/31/41/61/91/125/121/16