DNA testing is a powerful tool that can not only trace relationships like paternity, siblingship, maternity, and grandparent age. Genetic Testing for health is an accurate tool that can be extended to measure your health care by identifying your genetic code and makeup that could potentially impact your health.
DNA genetic testing can help you determine if you have a family history of certain diseases that can be passed on through genes to children. It can tell you if you may be more prone to cancer, diabetes, or heart and other health outcomes. Suppose there are genetic diseases like Tay-Sachs, Sickle cell disease and many others that are genetically prone to be passed on between generations within a family.
Empowering Health Choices with Genetic Data
The definition of genetics is the analysis and study of genes, and the definition of genes is the genomic process of understanding genes. Most human beings have a baseline of genetics that do not vary between human beings. The variant (about 1%) is what makes individuals different. A very small percentage of the genes impact your DNA and health outcomes. It is also important to note that genes are not only passed through ancestry but that environmental factors play a role in influencing your genetic and health outcomes.
The 1% variant is what will assist in the DNA testing for health outcomes. It will help you manage your health proactively with early testing. The importance of focusing on genes that are passed down through a family does not necessarily mean that a person will get a disease their parent had. Still, it indicates that the person has a higher risk of getting the disease than another person who does not have an ancestral heritage of the disease. DNA testing for these health outcomes is very helpful in determining the potential of individuals in the high-risk categories.
Genetic testing for your health can also help if you do not have any insights into your family health history.
What does a DNA Genetic Health Testing provide?
A genetic DNA health test is one of the most critical indicators to provide you with information on your family history. There are over 4 million variants in the human genome. These vary depending on ethnic backgrounds.
Having this information a person can make informed decisions on health conditions that will / can be passed down from parent to child and again from the child to their children etc. This potential health exposure tree can be managed before passing on the disease.
Tay-Sachs is an example of an inherited metabolic genetic disease that cannot be cured but can be managed throughout the life of a person. An estimated 5,000 people in the U.S. have the disease. The specific reason relates to a genetic change that prevents lysosomes from removing the toxins in the human body, impacting the brain and spinal code. If this disease runs through families, it would be beneficial for them to know so they can make decisions in the future.
How Accurate are Home-Based DNA Test Kits?
At-home test kits measure fewer genetic health markers than a lab-based test. The Food and Drug Administration does not regulate them, and the test results can be inconclusive. Getting your DNA health test at a reputable lab is best to get the right results.
Health risks are influenced by other factors apart from just a person’s genetic makeup. Environmental factors, diet, exercise and employment exposure can influence genetic conditions. Other factors include some variation between companies and how they perform genetic testing. It is very important to select a company that is AABB certified to really get the right approach to genetic testing.
SmarTest Labs, an AABB-certified lab, has trained employees who can guide you through the journey of selecting the right test for you with personalized assistance.
Call SmarTest Labs at 301-928-4136 to better understand the relevant test for you.
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