Clinical Tests

Our clinical tests include genetic predisposition health testing. These tests will help optimise your health and medically assist you in different ways, depending on the test you choose.

EasyDNA offers a range of cutting-edge and highly scientific genetic tests which fall under our clinical and molecular testing portfolio.

LKR282,600

Inherited Diseases Panel

Our Inherited Disease Panel tests for over 300 genes with over 700 unique inherited diseases, including neuromuscular, cardiovascular, developmental, and metabolic diseases and is often used to show a genetic compatibility between a couple or exclude it.

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Alzheimer’s & Dementia Panel

This test screens for mutations in 17 genes that can cause early onset dementia. The results from this screening test can aid in diagnosis, provide additional information to an already diagnosed patient and to identify potential risk genes causing dementia in the family.

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Cystic Fibrosis

Cystic fibrosis is a condition which mainly affects the lungs and pancreas, but can affect other parts of the body, including the liver, nose and sinuses, reproductive organs, and sweat glands. Our Cystic Fibrosis testing is performed using massive parallel sequencing (next generation sequencing) which allows for the analysis of exons, intron-exon boundaries, and UTRs that contain common mutations in the CFTR gene. This methodology with sequence analysis of all exons, intron/ exon borders, promoter regions, and specific intronic regions detects more than 98% of CFTR mutations.

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Inherited Cancer Panel

Our Inherited Cancer Panel specifically looks for inherited gene mutations in over 130 different genes associated with a wide range of hereditary cancers (including BRCA1, BRCA2 & PALB2). This screening test can be used to identify gene mutations responsible for hereditary cancers and to clarify the genetic risk for individuals with a family history of these hereditary cancers. It is a powerful tool that can help you reduce your risks or undertake measures that will help you detect hereditary cancers as early as possible.

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