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The Clinical Genomics Program at Stanford Medicine is a partnership between Stanford Health Care and Stanford Children’s Health that harnesses the power of genomic sequencing and precision health through our expert team of physicians, scientists and other genetics professionals. Genomic sequencing is the essence of precision health, understanding disease at a deeper level so that we can treat it more precisely. The Clinical Genomics Program at Stanford Medicine performs whole exome sequencing and other genomic testing services for patients with undiagnosed, genetic conditions.
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Stanford Health Care is known worldwide for the advanced patient care provided by its doctors and staff. We also provide a wide range of guest services and amenities to our patients and visitors. Learn more about preparing for a hospital stay, billing and financial services, and our other support programs in Patients & Visitors.
Stanford Health Care provides comprehensive services to refer and track patients, as well as the latest information and news for physicians and office staff. For help with all referral needs and questions, visit Referral Information.