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. Author manuscript; available in PMC: 2014 Jul 28.
Published in final edited form as: Hastings Cent Rep. 2012 Jun 20;42(4):28–40. doi: 10.1002/hast.50

Table 1. Potential Prenatal Testing Categories.

Type of information Does it inform reproductive decision-making for current pregnancy? Might the future child have an interest in not knowing the information? Could it provide immediate benefit to the future child?
Variants of unknown significance (genetic variations whose association with disease risk is unknown) No Yes No
Nonmedical genetic markers (genetic variations that have no health-related significance) No Yes No
Carrier status (possession of genetic variations that do not cause illness in the carrier but might contribute to illness in the carrier's offspring) No Yes No
Susceptibility genes (genes with variants that indicate increased likelihood for developing a condition) Sometimes Yes No
Late onset genetic conditions (highly penetrant genetic conditions that display no symptoms until late in life) Sometimes Yes No
Medical conditions found by current prenatal genetic tests (conditions with 100 percent penetrance that seriously affect health and quality of life throughout the life cycle) Yes NA Sometimes