Trusted by teams at
Get your genetic baseline to use alongside labs, wearables, and lifestyle data to prioritize the actions that matter most.
Starting at $49. One-time kit. No subscription required.
Whole-Genome
Sequencing-Based
1M+
Samples processed
Raw Data
Download anytime
Genetics in context
Start with your genetic baseline, then layer in periodic labs, daily wearables, and evolving lifestyle habits to build more personalized health insights.
See what you'll learnWEARABLES & VITALS
(Daily)
LABS & BIOMARKERS
(Periodic)
GENETIC BASELINE
(Stable Foundation)
Trusted by teams at
Simple Process
From order to insights in three easy steps. Everything is handled for you.
Step 1
We ship a simple saliva collection kit directly to your door. No blood draw needed.
Step 2
Provide your saliva sample and mail it back with the prepaid return label. That's it.
Step 3
Receive your personalized results and download your complete raw sequencing data.
What you'll learn
Start with 9 DNA-based health insights across core health areas. Ancestry is included too, as an added benefit.
This is just the start: more insights and traits are coming soon.
Your DNA baseline becomes even more useful when paired with labs, wearables, and the health data you already track.
Built for action
Personalized PRS report across key health traits
At-a-glance summary of High risk vs Not high risk results
Recommended next steps for each result
About this trait, technical details, and references for added context
Informational only; reflects relative genetic risk compared to a reference population and is intended as a starting point for conversations with your healthcare provider.
Example report
Privacy
Download your raw data anytime. Your genetic data is stored securely, with clear privacy practices you can understand.
Raw data download anytime
Private and secure data handling
Clear privacy practices
Pricing
One-time price. No recurring subscription required.
$49
The Difference
Most consumer tests use microarray chips that read only a tiny fraction of your DNA. We sequence it.
FAQ
No. This product is informational and educational only, and not a diagnostic test or treatment plan.
No. Results indicate genetic predisposition, not certainty. Lifestyle and environment still matter.
Polygenic Risk Scores (PRS) combine the effects of many genetic variants to estimate your predisposition toward specific health traits or conditions. They provide a single number that represents where you fall on a risk spectrum relative to the general population.
Low-pass whole genome sequencing (lpWGS) reads your entire genome at low coverage (~0.5×), then uses advanced imputation algorithms to fill in the gaps. This approach delivers genotyping-array accuracy at whole-genome breadth, capturing millions more variants than a traditional chip — all at an affordable price.
Results are typically available 4–6 weeks after we receive your sample. Our automated pipeline processes your data as soon as it arrives, and you will be notified by email when your report is ready.
Your genetic data is encrypted at rest and in transit. We do not sell, share, or provide your data to any third party. You retain full ownership and can request deletion at any time.
Yes. You can download your raw data anytime.
Use your genetic baseline to prioritize the actions that matter most.
Start with your baseline