Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a genetic condition and whether it can be passed on. I believe the benefits of genetic testing outweigh the cons. The physical risks of genetic testing are very small. A positive genetic test result can help a person maintain prevention and treatment options. Some test results can also help people make decisions about having children. Newborn genetic screenings can help identify genetic disorders early in life so that treatment can be started as early as possible so that the unwanted gene is not passed on. Most of the opinions in the seminar on genetic testing were positive, choosing that it should be used more often. Generic tests can help better prepare people for what they may pass on if they choose to have children. For example, if someone has a high risk of diabetes in the family, they are very likely to pass it on to their children and even contract it themselves. I think most people want to know what their genes carry, because it can have a huge impact on their life. Technological advances in genetic testing offer parents new information about their children's risk factors for developing diseases later in life. The issue has been the subject of heated debate as parents grapple with the pros and cons of testing themselves and their children. Genetic testing can help people determine why they get cancer or other diseases. Genetic testing is recommended for people who have a family history of a genetic disorder, have children born with genetic defects, and have suffered more than one miscarriage in the past. Although these… half of the document… an idea to take part in. Genetic testing can lead to comprehensive preparation for parents to care for their children. Genetic test results can determine a lot about children and what they may be passing on, whether it be diabetes, cancer, or any other illness or disease. For example, if someone is of Jewish descent they have a higher prevalence of BRCA1 and harmful BRCA1. BRCA2 mutations compared to people in the general population. Other ethnic and geographic populations around the world, such as the Norwegian, Dutch, and Icelandic peoples, also have higher prevalences of specific harmful BRCA1 and BRCA2 mutations. Additionally, limited data indicate that the prevalence of specific harmful BRCA1 and BRCA2 mutations may vary among individual racial and ethnic groups in the United States, including African Americans, Hispanics, Asian Americans, and non-Hispanic Whites..