![]() The sample is sent to a laboratory that will sequence your DNA and provide the autosomal DNA results from the genetic test. You do this with a spit, cheek swab, or blood. The first step to an autosomal DNA test is to provide a DNA sample through DNA kits. ![]() Through an analysis, an autosomal DNA test can determine who are your close relatives and even go several generations back and also determine your most common ancestry.Īutosomal DNA testing can be used to determine predispositions and find relatives. You manifest the trait or condition.Īutosomal DNA testing will look into these 22 pairs of autosomes. You inherit an affected gene from both parents.You do not inherit any affected genes from any of your parents.You do not have the condition, but you are a carrier. You inherit an affected gene from one parent but not the other.There are three ways in which an autosomal recessive trait or condition can happen: If you have children, you can pass on this affected gene to them. If one of your parents passes on to you an affected gene but the other passes on an unaffected one, you still carry this gene, of course, but you do not manifest it. This means that you need both of your parents to pass it on to you to have the condition. A very common autosomal recessive disease is cystic fibrosis. Autosomal recessiveĪn autosomal recessive trait or condition will only manifest if you inherit it from both of your parents. Some common autosomal dominant disorders include Marfan syndrome and Huntington’s disease. You can still get an autosomal dominant disease even if none of your parents has it when a mutation occurs. You do not have the condition or trait if both of your parents pass on an unaffected gene.įor an autosomal dominant condition to manifest, you only need to inherit it from one of your parents.You have the trait or condition if you inherit the gene from one of your parents only.If a given condition (a trait or a disease) is dominant, the offspring only needs one gene from one parent to have the trait or condition. These are autosomal dominant and autosomal recessive. Within the 22 autosomes, there are two categories of genes or conditions that are passed onto the offspring by their parents. Let’s quickly break down the types of autosomes to understand better how the tests work. Autosomal dominant vs autosomal recessive It is the small variations that determine your traits and genetic makeup, including the ones you inherit. Interestingly, 99.9% of this information is identical in every human being. This is the portion that autosomal DNA tests decode and analyze. Sex chromosomes are composed of the X and Y chromosomes, and humans typically either have two X chromosomes or an X and a Y chromosome.Īutosomal chromosomes make up the other 22 pairs and contain about 20,000 genes. Autosomal DNA tests analyze the autosomes.
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