Linking genetic data with electronic health records in hospital biobanks promises to advance precision medicine, but limited ancestral diversity constrains discovery and generalizability. We analyzed 93,936 participants from the UCLA ATLAS Community Health Initiative to inform disease prevalence and genetic risk across five continental and 36 fine-scale ancestry groups. We discovered numerous unreported gene-phenotype associations, including FN3K with intestinal disaccharidase deficiency in Euro
Advancing precision health discovery in a genetically diverse health system
Roni Haas·Daniel H. Geschwind·Christa Caggiano·Maryam Ariannejad·Timothy S. Chang·Paul Tung·Michael E. Broudy·Vishakha Patil·Ruhollah Shemirani·Takafumi N. Yamaguchi·Lawrence O. Chen·Danielle B. Martinez·Yash Patel·Mohammed Faizal Eeman Mootor·Michael Margolis·Tram Tran·Rupert Hugh-White·Nicole Zeltser·Angela Wei·Shafiul Alam·Sandra Lapinska·Veronica Tozzo·J A Feng·Prapti Thapaliya·Lora Eloyan·Alex A.T. Bui·Paul T. Spellman·Mao Tian·Noah Zaitlen·Paul C. Boutros·Bogdan Pasaniuc·Clara Lajonchere·Eimear E. Kenny·Jaron Arbet·Valerie A. Arboleda·Katelyn J. Queen

