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.
Could a rare disease
be the answer?
Genetic testing
can help you find out.
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.
Explore reanalysis"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."
