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Explore real variant classification running on a public reference genome to see how Humanome.AI works. No account needed.
The same outputs a Humanome run produces — shown here on the NA12878 reference genome
See how genetic variants are classified using ACMG guidelines - from Benign to Pathogenic
Understand carrier status for genetic conditions and disease risk factors
Your results stay current as new research is published - we notify you of changes
Your data is encrypted and never sold. Download or delete anytime.
The planned consumer flow once public ordering opens. Today the same pipeline runs on the reference genome above.
Select from Lite, Standard, or Concierge, then book a simple sample collection at a partner lab. The Quest Diagnostics integration is in development ahead of public launch.
The partner lab will sequence the whole genome (30x coverage for Standard/Concierge), with results expected in 2-4 weeks.
Results appear in an easy-to-understand dashboard. Every variant is classified using ACMG guidelines with clear explanations of what it means.
With a Sentinel subscription the genome is re-scanned monthly. If a new ClinVar release changes a classification, you will be notified.
Humanome is built on whole genome sequencing (30x coverage) — reading the whole genome, not the limited SNP panels used by 23andMe or Ancestry. Clinical validation is a prerequisite we are completing before public launch.
| Feature | Humanome.AI | 23andMe/Ancestry |
|---|---|---|
| DNA Coverage | 100% (Whole Genome) | <1% (SNP chip) |
| Sample Collection | Clinical Blood Draw | At-home Saliva |
| Lab Certification | Quest CLIA/CAP | Consumer-grade |
| ACMG Classification | - | |
| Continuous Updates | Monthly Re-scan | One-time report |
| Full VCF Download | Limited |