Genomics / Clinical interpretation
Genetic information.
A more informed picture.
Your genome adds information that can sharpen the clinical picture. We interpret it alongside your history, measured health, and goals to refine recommendations and identify what deserves closer attention.
Explore the projectFrom variation to interpretation
What does a finding change?
Genetic information can shift clinical probabilities and help refine a recommendation. We bring it together with family history, laboratory results, and measured physiology to understand what a finding means for you and what to consider next.
Inherited risk
Which findings change the starting picture, and how much confidence should we place in them?
Clinical context
How does genetic evidence fit with family history and the health information already available?
Evidence quality
What supports an interpretation, who was studied, and where might the evidence not apply?
Implications for care
Does a finding warrant further review or confirmation, and would it change a clinical decision?
Cardiovascular genomics
Explore your
heart genetics.
Our cardiovascular genomics tool reads a 23andMe or AncestryDNA raw data file and explains selected markers across nine heart pathways: LDL and ApoB, Lp(a), triglycerides, cholesterol absorption, the artery wall, blood pressure, heart rhythm, and how the body handles statins and clopidogrel.
Your file is read in your browser and is never uploaded. Seeing the report for your own file needs your name and email; a fictional sample report is open to everyone. The report is educational and is not a clinical genetic test.
Fifty markers across nine pathways, with the mechanism, evidence and DNA calls behind each finding.
Open the tool