Events
Run for Rare 2026: One cause. Thousands of steps.
enGenome takes a step towards raising awareness for rare diseases by organizing a special run event on February 28th, 2026
14 January 2026

On Saturday, February 28th, 2026, enGenome will host the annual Run for Rare at Parco Lambro in Milan. This is an event to bring people together to raise awareness and show support for those living with rare diseases.

Why we run

More than 300 million people around the world live with a rare disease. For many, the journey to diagnosis is long, uncertain, and often isolating. Early diagnosis can be life-changing. It means earlier care, better support and renewed hope.

At enGenome, we’re committed to shortening that journey through advanced genomic tools that help clinicians reach a diagnosis faster and with greater accuracy. Run for Rare is our way of standing beside patients and families, and inviting our community to do the same.

Event Details

  • Date: Saturday, February 28, 2025

  • Time: 9:30 am - 13:30 pm

  • Location: Parco Lambro, Milan

  • Entrance: Via Pusiano, in front of Ristorante Pizzeria al Parco (Via Pusiano, 63, 20132 Milano MI)

Participants can choose between a 5 km route for experienced runners or a 3.5 km route designed for beginners. Both runners and walkers are welcome to join—what truly matters is showing support for the cause.

What Participants Can Expect

  • A free t-shirt for everyone who registers

  • Light breakfast and water at the finish line

  • A meaningful experience that combines fitness, community, and purpose

Participation in the Run for Rare is free, but registration is required to secure a spot and receive a t-shirt.

Save the date, lace up your running shoes, and join us at Parco Lambro. We can’t wait to see you there!

About enGenome

enGenome offers innovative solutions for interpreting sequencing data. eVai, the flagship product, is a cloud-based solution fueled by artificial intelligence, that excels in prioritizing genetic variants and has been awarded by the NIH-funded CAGI6 challenge as best performing predictor, elevating diagnostic yield by 12.5%.

The latest release is VarChat, an open-access platform integrating Generative AI that searches and delivers informative text from current scientific literature on genetic variants.

Know more about the Rare Disease Day

Media Contact: Giovana Herold - marketing@engenome.com