The test targets and analyses genes with high hereditary cancer risk. By finding out the cancer-causing gene(s), it helps you to understand your risk of getting cancer, hence, enables you to start planning for cancer prevention and risk management in order to reduce that risk.
Steps | Accuracy |
---|---|
DNA sequencing | 99.9% |
Variant calling – SNP | >99%*# |
Variant calling – Indel | >99%*# |
* Passed GenQA/UK NEQAS external quality assurance
# The interpretation of sequencing variants is based on the current understanding of the variants at the time it was observed, which may change over time as more information about the genes becomes available. Not all variants are represented in this report.
More ways to shop: All Codex Genetics products are also available to order at all 9 Hong Kong Health Check Centres. Contact us for more details.
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