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“In the age of individuality and consumer empowerment some people want to take things into their own hands, but that’s not without its risks,” he said. According to an article written by Professor Harvey and Dr Basia Diug from Monash’s Medical Education Research and Quality unit, the tests “usually involve the collection of cellular material from cheek swabs or saliva which is sent to a laboratory that analyses the DNA." These are different to clinical services that are ordered by a GP. Are results from home-tested DNA safe and reliable? You can now spit in a jar, send it off and find out what your chances are of developing genetic diseases or depression or even a drug addiction. Michael Hing asks, “Is it worth it?” President of Syndromes Without A Name (SWAN), Heather Renton, whose daughter was diagnosed with FOXP1 Syndrome after two misdiagnoses, says everyone has a few so-called “dodgy genes." “You might have a gene susceptible to breast cancer the older you get, but as a 20-year-old you have no idea you’ve got that,” she said. After going through two misdiagnoses, she says she understands why some people would use these tests. “People are sometimes so desperate for answers,” she said, but “who’s to know that it’s credible - you might think you’ve got this gene and it might turn out that you don’t.” Regulators are starting to catch up to the technology. A framework introduced in 2010 forced manufacturers to get a conformity assessment certificate from the Therapeutic Goods Administration. As of July 1, local laboratories will have to develop standards for their tests to abide by, which will have to be accredited by independent authorities. That same month also sees the introduction of a new Life Insurance Code of Conduct. But Professor Harvey says overseas providers aren’t subject to the same conditions as local companies, and can get away with more.

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