Blood Testing Services
Genetic Insights
DNA analysis for inherited conditions, cancer risk, and nutritional genetics
← Back to All PanelsTip: Click on any biomarker tag to learn what it measures and why it's important for your health.
Unlock the secrets of your DNA to understand how your genetics influence nutrition, metabolism, and lifestyle factors. This comprehensive genetic panel analyses key genes that affect how you process nutrients, respond to exercise, and metabolise caffeine and other substances.
Determine whether you have a genetic predisposition to lactose intolerance. This test analyses the LCT gene which controls lactase production - the enzyme needed to digest lactose in dairy products. Understanding your genetic status helps guide dietary choices.
Screen for genetic markers associated with coeliac disease susceptibility. This test analyses the HLA-DQ2 and HLA-DQ8 genes which are present in virtually all coeliac disease patients. A negative result essentially rules out coeliac disease.
Screen for the most significant hereditary cancer risk genes. This core panel focuses on BRCA1 and BRCA2, which are associated with significantly elevated risks of breast, ovarian, prostate, and pancreatic cancers. Early detection enables proactive health management.
Comprehensive genetic screening for multiple hereditary cancer syndromes. This extended panel analyses genes associated with breast, ovarian, colorectal, prostate, pancreatic, and other hereditary cancers, providing a complete picture of your genetic cancer risk.
Screen for genetic variants associated with inherited cardiac conditions. This panel analyses genes linked to cardiomyopathies, arrhythmias, and familial hypercholesterolaemia, helping identify those at increased risk of sudden cardiac events.
Individual Genetic Biomarker Tests
Single gene tests for specific concerns
Tests for APOE gene variants (ε2, ε3, ε4) linked to Alzheimer's disease risk and lipid metabolism. The ε4 variant is the strongest genetic risk factor for late-onset Alzheimer's.
Tests for the Factor V Leiden mutation, the most common inherited cause of excessive blood clotting. Important for those with personal or family history of blood clots.
Tests for the prothrombin gene mutation associated with increased blood clot risk. Often tested alongside Factor V Leiden for complete thrombophilia screening.
Tests for hereditary haemochromatosis mutations (C282Y, H63D) causing iron overload. Early detection prevents organ damage through regular blood donation or phlebotomy.
Tests for UGT1A1 gene variant causing Gilbert's syndrome, a benign condition affecting bilirubin metabolism. Explains intermittent mild jaundice during illness or fasting.
Tests for alpha-1 antitrypsin deficiency, an inherited condition increasing risk of early-onset emphysema and liver disease. Important for those with unexplained lung or liver problems.
Frequently Asked Questions
Common questions about genetic testing