Carrier Report
Did you know that you may be carrying a disease trait in your genome without you knowing? Certain genetic variants in our DNA may cause genetic disorders, but we also may just be carriers for it. Whether you are starting a family soon, or just want to explore yourself more, find out if you are a carrier for inherited genetic conditions.
This report is compatible with raw DNA data from LifeDNA, 23andMe, Ancestry and MyHeritage users. Other users may not benefit as much from this report
What's the Importance?
Knowing your carrier status for a genetic disease is important because you may pass this mutation down to your children. If you and your partner are both carriers, there is a 25% chance one of your children manifests the disease and a 50% chance they also become carriers.
The studies performed on this genetic trait are highly reliable. There is a strong statistical significance between these genetic markers and the results in your report.
Several studies were conducted on these traits and they are deemed to be statistically significant in terms of frequency, however, more research is needed for the existing results to be deemed conclusive.
These traits are based on suggestive research, wherein only small population sizes and descriptive statistics were used to prove the studies' hypotheses.
Improve Your Body, Health, and Immunity with Your Own DNA.
Recurrent fever
Slow developmental delay
