The first ethical implication has to do with who owns and controls the genetic information. In most cases, the relevant specialists are the custodians of the information but the issue here is when the genetic information becomes part of the individualâ€™s medical record he or she is likely to be denied insurance coverage, employment and any other beneficial opportunity available. Second issue is the way disclosure of the genetic information affects the family.
The issue here is on the likely effect the information will have on the victim and how the larger society will perceive the individual, hence are mechanisms in place to ensure the individual or the family is not stigmatized? Thirdly, are the patients undergoing the genetic testing properly provided with information on the risks and shortcomings of the genetic technology? In most cases, this has not been adhered to.
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