How Smart Summary Organizes Your DNA Results
Updated: Oct 2
GenesUnveiled Smart Summary brings supported genetic markers and key findings together in one clear table. Instead of searching through a raw DNA file one rsID at a time, you can review more than 150 variants, along with your genotypes and personalized interpretations based on your active file.
Already analyzed your DNA file?
Open Smart Summary to review the supported markers and findings available from your results.
What Smart Summary shows
Each available row contains four main fields:
Gene
SNP ID
Your Genotype
Your Result
Results may include a typical finding, a higher or lower tendency, or a research-based relative-risk estimate where the source evidence supports one. Interpretations are straightforward and are primarily based on information from SNPedia and the GWAS Catalog.
Important to know: A result of 1× is similar to the reference population average, while 1.5× or 2× represents a higher relative estimate at that marker. These numbers describe statistical associations. They are not the same as an absolute probability of developing a condition.
Filter the table around what matters to you
Smart Summary includes tools that make a large marker table easier to review.
The category filter lets you narrow the table to a specific report area rather than viewing every available result at once. The Show Key Findings option can also help surface findings that may deserve closer attention.
These filters change how the table is displayed. They do not diagnose a condition or establish that one finding is medically more important than another.
How Smart Summary differs from full reports
Smart Summary is intended to provide a concise and quick overview.
A row may tell you:
which marker was detected
which genotype appears in the file
the associated result
the relevant gene or category
Full reports provide more context, such as the biological mechanism, evidence quality, research limitations, and a broader explanation of what the result may mean. Smart Summary is therefore useful for reviewing many single markers efficiently.
Comments