Discover your genetic characteristics to understand how to better manage your health.
Our Health analysis includes the study of thousands of genetic variants associated with various health conditions.
How do we analyze your health?
Your raw ancestry test data file contains information on approximately
600,000 DNA base pairs, which correspond to the nucleotide bases A, T, C, and G.
In fact, not all of this information is considered informative for ancestry.
A significant
portion of this data
relates to your
health traits.
SNPs (Single Nucleotide Polymorphisms) are the simplest form of variation in our DNA.
Thousands of SNPs are known to confer genetic traits such as eye and skin color, disease resistance, as well as many other health and nutritional characteristics.
On average, we report approximately 50,000 SNPs in your raw DNA data, related to over 2,500 genetic conditions.
Risks polygenic
Many genetic predispositions are caused by the combination of multiple SNPs. These are known as polygenic conditions.
We calculate your Polygenic Risk Score (PRS) for various diseases such as Alzheimer’s, anemia, breast cancer, hypertension, and many others.
Report examples
Your genetic variants (SNPs) are grouped into panels,
such as Nutrition, Muscular, Hormonal, Cardiac, and many others.
You can view the analysis details, identified SNPs, genetic interpretation, condition descriptions, and multiple scientific references for further exploration.
Polygenic risks.
We calculate your polygenic risk score (PRS) for dozens of genetic conditions, which quantifies how your genetic profile compares to the broader population.