The Rare Disease Watchlist: 9 Sessions Worth Watching

Behind every ambiguous genetic variant, negative diagnostic test, and unresolved case is a patient and family waiting for answers.

For clinicians, finding those answers can mean navigating increasingly complex genomic testing options, interpreting uncertain variants, and keeping up with a rapidly evolving field — all while managing the demands of everyday clinical practice.

So instead of adding another long reading list to your workload, we did the watching for you. We reviewed more than 50 hours of global genomic conferences, expert webinars, and clinical education sessions to curate 9 high-value sessions for healthcare professionals working in rare disease and clinical genomics.

From complex pediatric cases and WES vs. WGS to variant interpretation and first-line genomic testing, the Rare Disease Watchlist brings together practical insights and expert perspectives you can explore at your own pace.

Whether you have 20 minutes between appointments or an afternoon to dive deeper, there’s something worth watching.

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What’s on the Watchlist?

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Keep Exploring. Keep Looking for Answers.

You don’t need to watch all nine sessions. Start with the topics most relevant to the cases and questions you’re facing today.

Whether you have 20 minutes to spare or want to dive deeper, the Rare Disease Watchlist brings together expert insights you can explore at your own pace.

And if you’re currently working through a challenging or unresolved rare disease case, you don’t have to navigate it alone.

The 3billion medical team is available for a 1:1 clinical consultation to discuss challenging cases, explore genomic testing strategies, and consider possible next steps.

Select “Others” as the inquiry category and enter “Watchlist” in the comments. We’ll send the watchlist straight to your inbox.