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Genetic Testing
BRCA1 and BRCA2 Mutation Detection by NGS (full coding region sequencing) (blood)
2 960 som
Turnaround: 7–14 business days
Blood draw — 80 som (included in packages)
Description
Hereditary oncogenetics: detects mutations that raise the risk of breast and ovarian cancer — full sequencing of the BRCA1/BRCA2 genes (NGS). Helps assess family cancer risk and plan monitoring and prevention.
When to Take This Test
- Cancer in close relatives
- Assessing hereditary cancer risk
- As ordered by an oncologist/geneticist
Preparation
- No special preparation needed
- Taken once — the result doesn't change over a lifetime
- Interpreted by a geneticist
This information is for reference only and does not replace a doctor's consultation.
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