At your next large family gathering, talking about past cancer diagnoses throughout the family tree could provide valuable insight about possible risks of inherited cancers.
Cancers of the breast and ovaries caused by genetic mutations.
Genetic evaluation and counseling involves a consultation that provides an individual's risk of acquiring inheritable conditions. Learn more about this service.
Lynch syndrome is an inherited genetic disorder linked to an increased risk of developing cancer, often at a younger age in life—especially colorectal cancer, and, for women, endometrial cancer.
If you have a health condition that is difficult to diagnose, or a family history of medical problems, your doctor might recommend exome sequencing for additional clues.
A genetic disorder of blood vessels that affects people of all ages and backgrounds.
Molecular diagnostics involves analyzing DNA or RNA for red flags that can pinpoint the potential emergence of a specific disease.
Neurogenetics uses genome sequencing to understand the cause of brain and nerve disorders, such as Alzheimer's, ALS and many others.
Huntington’s disease is a rare, inherited neurodegenerative condition that slowly and permanently robs a person’s physical and mental health.
A rare, fast-growing type of cancer that begins in the brain and/or spinal cord.