AI-powered
genetic testing

for rare disease diagnosis

You're treating a patientwho has spent yearswithout a diagnosis.

You've tested for onesuspected condition afteranother, but still have noclear explanation for theirsymptoms.

Without a diagnosis, it'sdifficult to determine theright treatment.

From 100,000 to one.

• EVIDENCEClassifies ~100,000 WES variants in 5 minutes on average.
  ACMG criteria · 98.4% sensitivity · 99.99% specificity
• 3CnetAI predicts pathogenicity for variants lacking evidence.
  2.2× higher sensitivity, improving VUS reclassification.
• 3ASCRanks candidate variants by symptom similarity.
  Causative variant in the top 5 in 96% of cases.
• GeneticistsOur team confirms the final diagnosis.
  A report with classification evidence and interpretation.

What about patients
who
still don't have a diagnosis?

We keep reanalyzing
undiagnosed cases
until a diagnosis is found.

"Continuously revisiting data from undiagnosed patients — that's the real strength. Clinicians simply
don't have much time to chase every new paper or reinterpret variants themselves."

Simple to order.
Precise in results.

Order in just a few steps.
We'll send the sample kit.

Place an order