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Genetic factors from both parents, as well as environmental factors, contribute to a child’s health and development. Genetic testing can help to identify some, but not all, genetic mutations that may be present in a donor’s DNA. Read More
It is important to have a full understanding of your donor’s genetic test results, the associated risks to offspring, and the limitations of the donor’s testing.
PLEASE NOTE: Donors who carry genetic mutations for cystic fibrosis (CF) are now accepted into our donor program as of 2021. As with other conditions that are inherited in an autosomal recessive manner for which our donors may be carriers, offspring are not at risk to be affected unless the biological mother also carries a mutation for the same condition.
Carrier screening is widely available and we strongly recommend that PRIOR TO SHIPMENT of your vials, you:
- Download your donor’s genetic test results and medical history profiles from our website.
- Discuss the donor’s genetic test results and medical history with your physician and/or genetic counselor so that you can be fully informed about the risks to your offspring, your testing options, and to verify that the donor’s results are appropriate for your reproductive plans.
You can locate a genetic counselor in your area at: http://www.nsgc.org
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