FAQs
Find answers to commonly asked questions about our genetic testing and services.
General Questions
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Carrier Screening Heading
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Cancer Screening Heading
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Jewish Genetic Testing
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How to get carrier screening?
Getting carrier screening is a straightforward process. We offer convenient at-home testing kits that can be ordered online. Once you receive the kit, you'll provide a saliva sample and send it back to our lab. A team of experts will analyze your DNA for various genetic mutations. After processing, which typically takes a few weeks, you'll receive your results. At jscreen, we also provide genetic counseling to help you understand your results and what they mean for you and your family planning.
Who should consider taking these tests?
These tests are for individuals age 18 and older. If you have questions, please contact us here. Hereditary cancer test: Anyone who is interested in learning about their inherited risks for cancer can take the test. Carrier screen: The Reproductive carrier screen is intended for people who are planning to start or expand their family and wish to know if they are at an increased risk of having a child with a genetic condition.
Should I consider testing if I don’t have a family history of any of these genetic diseases?
Yes. The vast majority of children with these diseases are born to parents who have no family history of that disease. Remember that carriers are healthy and usually don’t have symptoms of the disease.
Should I consider testing if I am not Jewish and/or my partner is not Jewish?
Yes. The panel includes testing for more than 260 genetic diseases that are commonly found in people with both Jewish and non-Jewish ancestry. Therefore, it is valuable for anyone planning a pregnancy.
What happens if I test positive?
While many people will test positive for at least one disease, only a small percentage of individuals/couples will find out they have a high risk to have a child with a genetic condition. The good news is there are options to help plan for a healthy baby, even with high risk results. A genetic counselor will walk you through your options such as:
- In vitro fertilization(IVF)/pre-implantation genetic testing (PGT-M)
- Use of donor sperm or egg
- Adoption or fostering
- Prenatal diagnostic testing during pregnancy
- Testing the child after birth and treating the condition, as needed or as available
It is best to meet with a genetic counselor or doctor before pregnancy to discuss reproductive options.
