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(Hereditary Risk Assessment)
Gain insight into your inherited risk for conditions like cancer, heart disease, diabetes, and more. Through comprehensive panels such as BRCA1/2, Lynch syndrome, and cardiovascular risk genes, we help identify what runs in your family so you and your provider can take proactive steps in prevention, early detection, and lifestyle modification.
(Genetic Testing for Athletic and Wellness Potential)
Whether you're a professional athlete or just focused on personal fitness, our sports genetics panel reveals how your body is wired to perform. Learn about your muscle composition, endurance potential, injury recovery, metabolism, and nutrient needs—so you can train smarter, recover faster, and reach your full potential.
(Carrier Screening and Reproductive Genetics)
Before starting or growing your family, carrier screening can detect if you and your partner carry genetic conditions like thalassemia, cystic fibrosis, or spinal muscular atrophy. Knowing this information helps you prepare and explore options to ensure the healthiest possible start for your children.
(Family Health and Preventive Planning)
Genetic insights can help you make informed decisions about your family’s long-term well-being. From understanding inherited risks to guiding health monitoring for children, our family-focused panels provide a foundation for preventive care and generational health planning tailored to your DNA.
Genetic sequencing at Yale Medicine revealed that Amanda Gonzalez‑Bunster, who had endured nearly two decades of unexplained health issues—such as severe hypertriglyceridemia, fatty liver disease, and pancreatitis—harbored a rare mutation in the PPARG gene, diagnosing her with familial partial lipodystrophy type 3. This mutation, which oc
Genetic sequencing at Yale Medicine revealed that Amanda Gonzalez‑Bunster, who had endured nearly two decades of unexplained health issues—such as severe hypertriglyceridemia, fatty liver disease, and pancreatitis—harbored a rare mutation in the PPARG gene, diagnosing her with familial partial lipodystrophy type 3. This mutation, which occurred de novo, explained her body’s inability to produce healthy fat cells and the resulting metabolic complications . As one of only about 31 people worldwide known to have this condition, her case was both extraordinary and medically significant . Armed with this diagnosis, doctors prescribed metreleptin—a leptin hormone replacement—which dramatically improved her energy levels and metabolic health.
Today, she reports feeling “miraculous” improvements and has reinvigorated her life and academic pursuits.
Bryan, a Florida-based software professional, endured 25 years of depression and multiple ineffective medications with debilitating side effects. During a particularly severe episode, his psychiatric provider recommended a genetic test, and within days of submitting a saliva sample, the results were in .
The report identified medications h
Bryan, a Florida-based software professional, endured 25 years of depression and multiple ineffective medications with debilitating side effects. During a particularly severe episode, his psychiatric provider recommended a genetic test, and within days of submitting a saliva sample, the results were in .
The report identified medications he should avoid and guided his provider to choose a better-fitting treatment, leading to significant mental health improvement.
Coupled with cognitive behavioral therapy, Bryan reports feeling approximately 80% better than he had in decades. He now describes the test as life-changing and highly recommends it for its clear clinical value.
When Ilene’s sister Laura was diagnosed with breast cancer at age 44, genetic testing revealed she carried a BRCA mutation linked to a high risk of breast and ovarian cancer. Ilene also tested positive for the mutation and chose to undergo preventive surgery—only to discover she already had early-stage ovarian cancer.
Thanks to her sister’
When Ilene’s sister Laura was diagnosed with breast cancer at age 44, genetic testing revealed she carried a BRCA mutation linked to a high risk of breast and ovarian cancer. Ilene also tested positive for the mutation and chose to undergo preventive surgery—only to discover she already had early-stage ovarian cancer.
Thanks to her sister’s diagnosis and the genetic testing that followed, Ilene’s cancer was caught before it became advanced.
Today, both sisters are cancer-free, and Ilene actively supports cancer awareness and research, grateful that genetic testing gave her a second chance at life.
High rates of consanguineous marriages in Jordan increase the importance of premarital and preconception genetic screening.
Cardiovascular disease is a leading cause of death in Jordan. Genetic testing can identify hereditary lipid disorders and cardiac conditions early.
Breast, colorectal, and gastric cancers are among the top cancers affecting Jordanians. Genetic testing helps in risk assessment and prevention strategies.
Jordan has a high prevalence of Type 2 diabetes and obesity. Genetic testing helps stratify risk and personalize prevention strategies.
Thalassemia is one of the most prevalent inherited blood disorders in Jordan and across the Middle East. Carrier screening and diagnostic testing are essential for early intervention and family planning.
Due to the rise in chronic conditions like hypertension, diabetes, and depression, many Jordanians are on long-term medications. Pharmacogenomic testing improves efficacy and reduces side effects.
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