Free Sample DNA Report Dashboard
This is GenomeNarrator's interactive dashboard, opened on the sample report: a real analysis of a public research genome (553,977 variants, analyzed against the ClinVar 2026-08-29 release), not anyone's personal results. No account or upload is needed to explore it. To see your own, upload a 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA or VCF file on the Genomic Report page. The sample's two bloodwork draws are illustrative, because a research genome comes with no lab results.
Eight tabs
- Report: a genome summary, a risk radar across six body systems, each condition's estimated risk against the population average, medication genes at a glance, the evidence behind each finding, hereditary gene findings, and every condition grouped by body system.
- Ancestry: composition with 95% intervals, the founder-variant panels screened, mtDNA and Y-DNA haplogroups with ancestral and migration paths, and chromosome painting across all 22 autosomes.
- Medications: how many of 100 common medications the genes affect, which genes drive it, the CPIC evidence level behind each, a Medicine Cabinet grouped by therapeutic area, and a checker for the drugs you take.
- Markers: bloodwork read against the genome, with a Testing Plan, a lab ledger with trends, Model Resolution, Genetics × Labs with tissue and pathway, gene-by-gene interactions, and Clinician Summary and FHIR exports.
- Lifestyle: four pillars (Nutrigenomics, Exercise Physiology, Sleep & Chronobiology, Mind & Behavior), each with a whole-genome polygenic score and a trait map, from 138 curated traits.
- Molecular Detail: gene constraint, tissue expression and pathways for each gene behind a finding.
- Timeline: every lab draw on one time axis, with changes tested against each marker's biological variation, and the genome as the lens they are read through.
- Compass: a PDF report builder, one chapter at a time or in full.
A section-by-section tour is at genomenarrator.com/llms-full.txt. See also pricing and how GenomeNarrator works.