RGI is a non-profit organization that provides research to families in need of diagnosis & treatment for rare genetic diseases.

Joined August 2011
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RG gives rare disease patients access to modern genomics sequencing technology, connections to scientists and researchers and philanthropic opportunities. Shortening the diagnostic odyssey is our core mission. To apply as a new patient, click here: raregenomics.org/how-we-help…
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RGs' Patient Research Services (RGPRS) connects rare disease patients to genomic research. When Ally’s family sought answers, RGPRS analyzed her genome and identified a histone-4 variant (H4C5) explaining her symptoms. Enroll as a new patient here: loom.ly/qt9fAv4
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