Genetic health screening
Whole exome sequencing · Health-check editionAnalyse the exonic regions of more than 20,000 genes to explore selected inherited disease risks, carrier findings and medication-response differences.
Identify selected inherited risks earlier to inform screening and intervention.
Findings can help clinicians tailor when and how often to screen, arrange further assessment and consider early intervention.
View details ↗What can it help
you understand?
Explore selected inherited health risks and turn relevant findings into more informed screening and health-management plans.
01Inherited conditions & carrier status
Inform family genetic counselling and reproductive planning.
02Hereditary cancer risk
Help plan more targeted screening and follow-up.
- Lynch syndrome · colorectal cancer risk
- BRCA-related breast cancer risk
- APC · familial adenomatous polyposis
- RET · hereditary medullary thyroid cancer
- CDH1 · hereditary diffuse gastric cancer
03Cardiovascular & metabolic risk
Provide clues for further assessment and earlier health management.
- Familial hypercholesterolaemia
- Selected inherited cardiomyopathies
- Selected inherited arrhythmias
04Medication-response differences
Help clinicians consider the choice and use of certain medicines.
Examples illustrate potential clinical uses. Reporting follows the laboratory’s analysis scope; results and next steps require professional interpretation.
Understand the test.
Make an informed choice.
See the illustrations, testing process and report details.