N1C Gene Registry

At N1C, we aim to advance individualized medicine by connecting the evolving ecosystem. The N1C Gene Registry (Version 1.0) is our first step in documenting genes, and specifically variants, under investigation, fostering visibility, coordination, and collaboration across academia, industry, patient groups, and nonprofits. By increasing transparency and reducing duplication, the registry supports ecosystem-wide awareness, accelerating the development of treatments for ultra-rare conditions.

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