
Although our DNA does not change, technology does. Our capacity for genetic testing has advanced from simple genotyping, which determines the genetic variants that an individual possesses, to genetic sequencing, which examines the exact order of DNA base pairs. In simpler terms, genotyping highlights specific spelling errors in a sentence, while genetic sequencing checks the whole sentence for mistakes, including grammar and spelling. As the capacity for genetic testing has increased (indicated in the increased detection rate from 90% to 99%), a large number of genetic conditions have been added to the panel.
Our genetic counselor, Scott Weissman, offers a piece of advice:
“Similar to other genetic tests, technology continues to improve, and we are learning more about genetic conditions every day. It’s the same for carrier screening. It’s no longer the “one and done” type of test that it used to be.”
This does not mean that you must get tested prior to each pregnancy. However, recognizing changes in family health history and keeping up to date with available options for pregnancy, especially if you are a carrier, is extremely important. By simply checking in with your OBGYN or doctor to discuss any changes/additions to the panel, you are maximizing your options when it comes to having a healthy pregnancy.
If you are considering getting screened, I recommend that you consider our carrier screening program. The Sarnoff Center offers an online, on-demand carrier screening program that you can complete from the comfort of your own home. Here is the link to the registration page and if you have any further questions, please contact Scott at 312-357-4985: jewishgenetics.org/get-screened
Resources:
- Genotyping vs. Sequencing: What’s the Difference? | Orig3n
- Carrier screening in individuals of Ashkenazi Jewish descent (nih.gov)
- Expanded Newborn Screening: Information and Resources for the Family Physician – American Family Physician (aafp.org)
Written by Lilli Arbetter
