According to genetics how is it possible for one family to have different blood groups types? ​

Explanation:

The Human Genetics Tutorial with problem solving exercises concerning the inheritance of the ABO blood group alleles has resulted in a steady stream on inquiries to the Biology Project from mothers, grandmothers, and children inquiring about the possible blood type of the father of a given child.

Human blood type is determined by co-dominant alleles. An allele is one of several different forms of genetic information that is present in our DNA at a specific location on a specific chromosome. There are three different alleles for human blood type, known as IA, IB, and i. For simplicity, we can call these alleles A (for IA), B (for IB), and O (for i).

Each of us has two ABO blood type alleles, because we each inherit one blood type allele from our biological mother and one from our biological father. A description of the pair of alleles in our DNA is called the genotype. Since there are three different alleles, there are a total of six different genotypes at the human ABO genetic locus. The different possible genotypes are AA, AO, BB, BO, AB, and OO.

A blood test is used to determine whether the A and/or B characteristics are present in a blood sample. It is not possible to determine the exact genotype from a blood test result of either type A or type B. If someone has blood type A, they must have at least one copy of the A allele, but they could have two copies. Their genotype is either AA or AO. Similarly, someone who is blood type B could have a genotype of either BB or BO.

A blood test of either type AB or type O is more informative. Someone with blood type AB must have both the A and B alleles. The genotype must be AB. Someone with blood type O has neither the A nor the B allele. The genotype must be OO.

Each biological parent donates one of their two ABO alleles to their child. A mother who is blood type O can only pass an O allele to her son or daughter. A father who is blood type AB could pass either an A or a B allele to his son or daughter. This couple could have children of either blood type A (O from mother and A from father) or blood type B (O from mother and B from father).

Since there are 4 different maternal blood types and 4 different paternal blood types possible, there are 16 differnt combinations to consider when predicting the blood type of children. If you know the blood type of the mother and father, the possible blood types for their children can be found.

The Rh factor genetic information is also inherited from our parents, but it is inherited independently of the ABO blood type alleles. There are 2 different alleles for the Rh factor known as Rh+ and Rh-. Someone who is "Rh positive" or "Rh+" has at least one Rh+ allele, but could have two. Their genotype could be either Rh+/Rh+ or Rh+/Rh-. Someone who Rh- has a genotype of Rh-/Rh-.

Just like the ABO alleles, each biological parent donates one of their two Rh alleles to their child. A mother who is Rh- can only pass an Rh- allele to her son or daughter. A father who is Rh+ could pass either an Rh+ or Rh- allele to his son or daughter. This couple could have Rh+ children (Rh- from mother and Rh+ from father) or Rh- children (Rh- from mother and Rh- from father).

gold i'm pretty sure i might be wrong

you didn't give any options but heres what i can tell you: an inference is likely to change based on additional observations. the latter is something that you have seen or sensed using your sensory organs while the former is like a conclusion out from what you have observed.