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What will a DNA test show you?



DNA testing is a great way to know about the health secrets of your body. The DNA test labs will analyze your DNA samples and will identify different changes that might be associated with some genetic conditions. Additionally, sometimes these DNA evaluations help doctors to identify some risks that might be associated with a disease. Other DNA tests might show if people are safe from some conditions. Similarly, DNA paternity testing determines or rules out if the alleged father is the biological father.

Have a deeper understanding of your health:

These days there are multiple DNA testing methods that are available at the clinical or consumer level. Most of the time, a mouth swab, blood test, or hair sample facilitates doctors and scientists to evaluate a person’s DNA for a mutation that might be linked with certain conditions or diseases.

In addition, you should also know that the consumer and clinical DNA testing methods are not created with equal credibility. Similarly, home DNA tests are not very standardized as medical DNA tests are. However, they are evaluated in the same DNA testing labs. Moreover, no matter what your requirements are regarding a DNA test, you should always talk to a physician about explaining the test results.

DNA testing confirming conditions:

In most cases, DNA testing methods are great for confirming or ruling out if there is a possibility of a certain genetic condition if they have specific symptoms. In the midst of a DNA test, an expert like a doctor or nurse will collect samples such as blood, saliva, skin, or hair from the patient. Similarly, pregnant women may also give a sample of amniotic fluid.

The NIH states that clinically available genetic methods can identify 2,000 diseases that are transferred from one generation to another. Some of the most common diseases that these genetic tests can find are muscular dystrophy, familial hyperlipidemia, and cystic fibrosis.

Additionally, the diagnostic DNA evaluation looks for some selected changes in the DNA, as these changes affect the functionality of that gene, and as a result, the person might develop a disease. These DNA testing lab results are highly accurate and reliable. Moreover, one of the best benefits of these DNA methods is that they help the doctor to identify health risks at the early stages of their development. As a result, when the condition is identified in the early phase doctor can help the patient in managing the disease. Similarly, it is very helpful in certain conditions like familial hyperlipidemia that can result in a premature heart attack and stroke. Catching these diseases in the early stages means the patient will have more capabilities to treat the disease. These tests are performed in a health care setting.

Presymptomatic DNA tests:

When a healthy person has a documented family history of a condition like diabetes, these DNA tests evaluate certain markers in the genes that are linked to that condition. This data will inform the doctor whether that person is at risk of developing the condition. One simple example is Huntington’s disease. It is a single-gene disorder that is responsible for dementia. Most of the time, this condition happens when someone is in their 50s or 60s. As a result, if you have a mutation linked with that disease, there is a 100% probability that you are going to get it. On the other hand, when a disease involves having multiple mutations happening in one or some genes confirming whether a person is at risk of developing a condition becomes quite complicated. Additionally, some conditions do not happen due to changes in a single gene; meanwhile, multiple mutations might be happening in multiple genes. as a result, DNA testing methods will be useful for doctors to evaluate whether someone will have the disease, how worse is it going to be and might even get some insights on the possible treatments.

Carrier Test specification:

Sometimes people who are perfectly healthy might have mutations in their DNA that might be linked with different genetic disorders. This condition is called being a carrier. In simple words, your gene carries a single copy of the gene mutation for the condition that has been transferred in your family from generations. In general cases, the conditions do not affect the person or their health as their DNA still has an additional copy of that same gene that does not have the mutation.

For the most authentic condition confirmation through DNA testing, you can visit Choice DNA. We have some of the latest technology along with a highly professional staff. Our paternity testing methods are very known and even court admissible.