For Patients
Join us and receive a personalized toolkit, crafted just for you by our expert team
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A personalized report summarizing the clinical context of your variant, gene, and condition
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We notify you when
Variant event (including reclassification)
Clinical trial launch
Therapy launch
Guideline change (e.g. Variant curation Expert Panel submissions)
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Get regular updates on the latest in genetics
Join us and receive the research feed, custom built for you by our team
Know your Variant
Up to 40% Variants of Uncertain Significance are reclassified over a 5 yea period. Stay up to date with our Allele Alerts. As discoveries happen, you’ll be the first to know
Be the Expert
Millions of scientific papers are published each year. Our experts keep you informed of what matters to you with a curated literature feed
Access treatment
Precision medicine can be prescribed based on your genetic testing results. Get exposed to personalized drugs or experimental treatments for your condition