Finding your way around your report
Clinically significant findings come first. An empty summary means nothing reportable was found, which is the most common result.
The report opens with a summary of anything clinically significant. If that section is empty, no reportable finding was identified which is the most common outcome and a good one.
Below the summary sit the detailed sections: hereditary risk, carrier status, pharmacogenomics, and traits. Only the first three are clinically reviewed. Trait results are for interest and should not guide decisions.
Each finding lists the gene, the specific variant, its classification, and the evidence behind that classification. The evidence links out to public databases so a clinician can check our reasoning.
A genetics report describes what was found in this test, not everything about your health. Sequencing has known blind spots, including some repeat expansions and structural variants.