Genetic Testing
Genetic testing examines an individual’s DNA to detect changes or variations that may indicate genetic disorders, inherited traits, or susceptibility to certain diseases. It provides insights into ancestry, potential health risks, and informs medical decisions. This analysis helps personalize healthcare and understand inherited conditions better.
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Cancer (CGx)
The Familial Cancer Panel identifies gene mutations related to hereditary cancers. Some inherited cancers include:
- Breast cancer
- Cervical cancer
- Colon cancer
- Prostate cancer
- Other cancers
Following the pattern of a hereditary cancer in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Cardiopulmonary (CPUL)
The Cardiopulmonary Disease Panel identifies gene mutations related to cardiovascular disease. Some inherited conditions include:
- High blood pressure
- High cholesterol
- Arrhythmia
- Cardiomyopathy (disorders that affect the heart muscle)
- Other cardiopulmonary disorders
Following the pattern of hereditary cardiopulmonary disorders in your family can help your doctor predict the likelihood of you or other family members having the same conditions.
Comprehensive Eye (EYE)
The Comprehensive Eye Panel identifies gene mutations related to eye disorders and retinopathies. Some inherited conditions include:
- Retinopathy
- Macular degeneration
- Glaucoma
- Cataracts
- Other eye disorders
Following the pattern of hereditary eye disorders in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Diabetes (DO)
The Diabetes Panel identifies genes mutations related to hereditary forms of diabetes. Some inherited diabetic conditions include:
- Type I Diabetes
- Type II Diabetes
- Gestational diabetes
- Other forms of diabetes
Following the pattern of hereditary diabetes in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Immunodeficiency (IMMUNO)
The Immunodeficiency Panel identifies gene mutations related to hereditary forms of immunological disorders. Some inherited conditions include:
- Primary immunodeficiency
- Rheumatoid arthritis
- Multiple sclerosis
- Hashimoto’s thyroiditis
- Other autoimmune disorders
Following the pattern of hereditary immune disorders in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Neurocognitive (NEURO)
The Neurocognitive Disorder Panel identifies gene mutations related to neurological disorders. Some inherited conditions include:
- Parkinson’s disease
- Alzheimer’s/Dementia
- Depression
- Anxiety
- Other neurological disorders
Following the pattern of hereditary neurological disorders in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Pharmacogenomics (PGx)
The Pharmacogenomics Panel identifies how a person’s genes affect the likely response to therapeutic drugs. Common drugs tested include:
- Cancer drugs
- Psychiatric drugs
- Cardiovascular drugs
- Pain medication
Knowing this information can help your healthcare provider find medication that will work best for you.
Pulmonary (PUL)
The Pulmonary Disorder Panel identifies gene mutations related to pulmonary disorders. Some inherited conditions include:
- Cystic fibrosis
- Interstitial lung disease
- Pulmonary artery hypertension
- Asthma
- Other pulmonary disorders
Following the pattern of hereditary pulmonary disorders in your family can help your doctor predict the likelihood of you or other family members having the same condition.
Thyroid (THY)
The Thyroid Panel identifies gene mutations related to thyroid disorders. Some inherited conditions include:
- Hypothyroidism
- Hyperthyroidism
- Goiter
- Thyroid nodule
- Other thyroid disorders
Following the pattern of hereditary thyroid disorders in your family can help your doctor predict the likelihood of you or other family members having the same condition.