Genome signals
Your whole genome is three billion letters of DNA. We sequence all of it at 30x depth, then translate the parts that matter into clear, personal findings, so instead of raw data you get answers you can actually use.
2,000+
signals
1,000+
diseases
30x
coverage
3B+
bases read
Gene library
Look up a gene, a condition, or a medication and see in plain language what it means for your body.
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900+ conditions
We compare your DNA against known risk variants for cancers, heart disease, diabetes, neurological conditions and more, then tell you in plain terms where your risk sits relative to the average person and what’s worth watching.
600+ conditions
You can be perfectly healthy and still carry a recessive variant that matters for your children. We flag carrier status for conditions like cystic fibrosis and sickle cell, which is especially useful before or during family planning.
300+ drug-gene pairs
Your genes change how you respond to common medications like blood thinners, antidepressants, statins, and painkillers. Knowing this ahead of time helps a clinician pick the right drug and dose instead of trial and error.
200+ traits
From caffeine metabolism to lactose tolerance to sleep and nutrition tendencies, these are the everyday signals that explain how your body actually works. Informative rather than urgent.
Not every signal deserves the same attention, so each one is ranked. Significant findings are always worth reviewing with a qualified clinician.
Higher-impact risks where earlier screening or a clinician conversation can genuinely change the outcome.
Findings worth keeping an eye on over time, or sharing with your clinician before a prescription.
Everyday traits about how your body works. Informative, not alarming.
One cheek swab. Whole-genome sequencing and a plain-language report you can explore.