Test Description

This test is designed to give you a full body of information on any chromosomal abnormalities you may have or may have inherited from your parents.

We screen your whole chromosomes against 4000 genes to reveal any hidden abnormalities known or unknown to you.

In addition, this test reveals a person’s risk of developing certain diseases, allowing for preventive measures and lifestyle changes.

The test can be used for diagnostic and screening purposes of any chromosomal abnormalities linked to your genome.

We screen for the following conditions

*Cancer (blood, breast, ovarian, prostate…)

*Cardiac (cardiomyopathy, heart arrhythmias, familial thoracic aortic aneurysm syndrome…)

*Neurology (autism spectrum disorders, developmental delay, intellectual disability, epilepsy, dyslexia, seizures, alzheimer’s, parkinson’s…)

*Blood (sickle cell, immunodeficiency disease, anemia…)

*Hearing loss

*Vision loss

*Skin condition

*Reproductive health (infertility in men, pregnancy loss…)

*Many other chromosomal abnormalities…

Benefits of this test

*Identifying genetic disorders early in life

*Allowing for early treatment and management

*Enabling informed decisions about healthcare and family planning

*Guide treatment decisions a provide a sense of relief for uncertainty

Who can order this test

Anybody can order this test and follow up with their healthcare providers. We have genetic counselors available who can go over your lab results and guide you about the next steps to take.

Test order

You can order the test directly by going to our online store or from your healthcare provider’s office.

*If the test is ordered directly through us, we will mail you a collection kit and a return label along with the collection and return instructions.

*If the test is ordered by your healthcare provider’s office, we will mail the collection kits and instructions to their office.

Results

We follow the Online Mendelian Inheritance in Man (OMIM) and American College of Medical Genetics and Genomics (ACMG) guidelines for reporting.

Any finds will be interpreted as followed:

Pathogenic

Likely pathogenic

VUS (Variant of unknown significance)

Benign

Likely benign

However, it is important to note that genetic testing has limitations and may not be able to detect all genetic defects. The genetic results do not necessarily mean that you will develop a condition. It identifies the genes or mutations that increase your risk of developing a particular condition.