Know the moment a new variant is found in your gene.
Get notified when new variants are submitted to ClinVar — new submissions, submitting labs, classification trends. For every gene.
Every alert gives you a path to the people who can find your patient
New variants in your gene, with the lab, clinician, trial PI, and advocacy org who matter — one click to start a conversation.
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Submitting lab outreach
Direct link to the lab's patient outreach or sponsor liaison program (Invitae PatientsMatter, GeneDx Study Sponsor, etc.)
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The treating clinician
When the variant is in a published case report, we surface the corresponding author with their contact info
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Enrolling trial PIs
For each gene, the Principal Investigator and trial coordinator of every actively enrolling clinical trial — already looking for these patients
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Patient advocacy org
The disease-specific patient registry and advocacy org with sponsor inquiry channels (CFF, Cure SMA, NF Foundation, NORD, etc.)
One click to start the conversation
Every contact in your alert has a direct Contact button — labs, clinicians, trial PIs, and patient advocacy orgs.