https://en.wikipedia.org/wiki/Chin
This is an inherited trait in humans, where the dominant gene causes the cleft chin, while the recessive genotype presents without a cleft. However, it is also a classic example for variable penetrance[15] with environmental factors or a modifier gene possibly affecting the phenotypical expression of the actual genotype. Cleft chins are common among people originating from Europe and the Middle East.[16]
http://www.thebrightesthub.com/what-causes-cleft-chin/
Overview of Cleft Chin Genetics
Cleft chin is a facial characteristic that looks like a dimple or an indentation to a persons chin. It is caused by the failure of the lower half of the jaw to fuse together during fetal development. It is an inherited physical trait which is observed more prominently in men than in women. In the general population, the number of people with cleft chins is lower than those with the normal chin (it doesnt mean that people with cleft chins are abnormal, they are in fact attractive). Like any of our facial characteristics (dimples, broad forehead, hook nose, etc.), genetics is what causes cleft chin.
Cleft chin is a dominant trait; it masks the expression of the gene for the normal chin. The masked gene is said to be the recessive gene and normal chin is the dominant trait. In genetics, a dominant trait is symbolized by a capital letter (C for cleft chin) while the recessive gene is symbolized by a lower case letter (c for normal chin).
In order for a child to have a cleft chin, he should at least inherit the gene for cleft chin from his parents. If the child inherits two cleft chin genes from his parents, he would develop cleft chin by being homozygous to the trait (CC). If he inherits only one cleft gene from his parents, he would still develop cleft chin by being heterozygous to the trait (Cc). If no cleft gene is inherited from the parents, the child will develop the normal chin.
If both parents are homozygous to cleft chin (CC x CC), there is a 100% chance that all their children would have cleft chins. If they are both heterozygous to the trait (Cc x Cc), their children have 75% chance of developing cleft chins. If one of the parent is homozygous to the trait (CC) and the other parent is recessive (cc), the childrens chance of developing cleft chins is 100 %. If one of the parent is heterozygous to the trait (Cc) while the other parent is recessive (cc), there is 50% chance (Cc x cc) that each of their children will develop cleft chins.
Take note that the percentages above were computed using the Punnet square. Learn more about Punnet square here.
[ad#co-1]
Genetic Factors that can Affect the Expression of Cleft Chin Trait
In theory, parents with cleft chins would have children with cleft chins since the trait is dominant. On the other hand, parents that do not have the cleft chins could not have children with the trait since they do not carry the genes for cleft chin. However, these instances are not always observed. It can happen that parents with cleft chins couldnt produce children with the trait and parents with no cleft chins could produce children with the trait. These phenomena are due to variable penetrance or the presence of modifier genes.
Thank you for clarifying!