Your Health, Your Future

Genomic Screening

Guidence around suitable genomic testing for you based on your personaslised health history.

Expert Medical Advice

Interpretation, counselling and support of pharmogenomic and genomic testing.

Disease Management

Intergrating genomic testing to inform ongoing medical care and diease mangement.

46

Chromosomes

20,000

Genes

30,000

Medical diseases
99.9% of the information in human genes is the same in all of us. Our differences arise from the 0.1% of unique genetic information we each have. Mostly this influences our characteristics and doesn't cause any problems.
Sometimes variations may influence your risk for some health problems. They may also predict how a person’s body reacts to, or metabolises (breaks down) different treatments or medications.

Wondering how genomics can change your healthcare ?

Gemomic Testing
These tests aim to find changes in your DNA (called varients) that may inflence your health and influence the risk of developing some diseases.
Pharmacogenics (Medicines)
Pharmacogenics looks at the way your DNA affects your response to medicines. Your genes influence how well the medication will work for you and may predict if you will have side effects from it.
NIPT - Non Invasive Prenatal Testing
Can be used to determin the risk of a fetus having certian chromosomal abnormalities (trisomy 21, trisomy 18 and trisomy 13) and can be preformed as early as 10 weeks.
Disease Risk and Stratification
Understanding your health risks and learn the strategies you and your doctor can implement to promote good health into your future.