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Genetic testing is now an extremely controversial issue among both the general population and the scientific community. It is a procedure which exposes a person's entire genome sequence, allowing it to be read and assessed to determine possible risks for hereditary diseases or ailments that may be passed onto offspring (Holt Productions, 2012). With tens of thousands of genetic tests currently being used, and more being established, it appears logical to place this growing technology to utilize. Some agree that it's a person's right to know and understand his or her genetic makeup. However, others argue that, regardless of the benefits of genetic testing, caution ought to be used to carefully inspect the risks associated with this new technology. Relatively simple tests can be used to run genetic testing on adults and kids; even fetuses can experience testing, but at higher risk for complications. Currently, genetic testing has to be ordered by a medical professional such as a physician, nurse practitioner, or medical geneticist. Once ordered, a DNA sample is delivered to a lab for further testing. In adults, sampling methods typically involve taking DNA through blood draws, hair pulls, skin samples, or samples of other tissues. In fetuses, however, there are two techniques which may be utilized to acquire genetic information: amniocentesis and chorionic villus sampling. During amniocentesis, amniotic fluid is removed in the placental sac and analyzed right. The other procedure is chorionic villus sampling, where a tissue sample is analyzed after being taken straight from the embryo (National Library of Medicine, 2014). Genetic testing has become a routine procedure to test teens for various genetic diseases. 1 such genetic disease that's routinely display...