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Sequencing the human genome was one of the major scientific achievements of the last 50 years. Now, this technology has transformed the way we approach and diagnose genetic disease. The Clinical Genomics Service at Stanford Medicine brings the power of genomic sequencing into the hands of our physicians and with it, the knowledge into the hands of our patients. At Stanford, we apply advanced genomic sequencing and expert interpretation to provide more personalized and precise clinical care.
Care and Treatment
Our team is comprised of clinicians in multiple disciplines from Stanford Medicine, bioethicists, genetic counselors, bioinformaticians, basic and translational researchers, and other experts in a variety of specialties. The Stanford Medicine Advisory Committee on Genomics provides support for the new service, with regular meetings to address critical issues of data storage, security, regulations and policies that apply to such testing.
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 Referring Physicians.
HOW TO REFER
Fax a referral form with supporting documentation to 650-320-9443.
Track your patients' progress and communicate with Stanford providers securely online.