Type
Genetic Testing
Duration
1 hour
What's included
5 deliverables in this treatment
- Pre-test physician consultation to clarify focus areas
- DNA SNP genotyping via Laboratoires REUNIS Luxembourg
- Personalised written report with variant explanations in plain Czech/English
- Lifestyle, diet and supplementation recommendations based on results
- Results consultation with MUDr. Hora interpreting findings
5P Medicine's predictive genomics service analyses single nucleotide polymorphisms (SNPs) to identify inherited predispositions to civilisation diseases — cardiovascular risk, metabolic disorders, certain cancers and neurodegenerative conditions — before any symptoms appear. DNA is processed in partnership with Laboratoires REUNIS in Luxembourg, one of Europe's leading specialist genomics laboratories. MUDr. Hora, who performed the first genomic examination in the Plzeň region back in 2009, interprets results in a detailed personalised report and translates genetic risk factors into actionable lifestyle, diet and supplementation recommendations. The key insight: predisposition is not destiny — environmental and lifestyle factors can modulate gene expression significantly.
About this treatment
Predictive genomics at 5P Medicine uses high-resolution SNP (single nucleotide polymorphism) profiling to map an individual's inherited susceptibility to a wide range of chronic conditions. Unlike a family history conversation, SNP analysis quantifies risk at the molecular level, identifying specific gene variants associated with cardiovascular disease, type 2 diabetes, obesity, selected cancers, thyroid dysfunction and neurodegenerative disorders.
The DNA sample (typically a buccal swab or blood draw) is sent to Laboratoires REUNIS in Luxembourg — 5P Medicine's partner since 2011 — where it undergoes comprehensive array-based genotyping. Results are returned to the clinic and interpreted by MUDr. Petr Hora MBA, who has been working in genomics since 2003 and performed the first genomic exam in the Plzeň region in 2009.
The process unfolds in three stages. First, a pre-test consultation clarifies which risk areas are most relevant for the patient's age, symptoms and family background. The sample is then collected and dispatched; analysis typically takes two to four weeks. Finally, a results consultation covers every flagged variant in plain language, cross-referencing current evidence on penetrance and modifiability. The written report includes a prioritised list of…
Good to know
- Technology
- SNP array genotyping
- Laboratory
- Laboratoires REUNIS, Luxembourg
- Experience
- First genomic exam in Plzeň region (2009)
- Report language
- Czech (English on request)
Who is this for?
Adults with family history of chronic disease; prevention-focused individuals; anyone with unexplained metabolic or hormonal issues
About the clinic
Reviews, team and credentials
Independent review links and clinic-reported team information.
Clinical team
The clinic is led by MUDr. Petr Hora MBA (born 1969, Plzeň), a Charles University Medical Faculty graduate with a background in anaesthesiology, intensive care and air rescue. Dr. Hora pivoted to genomics and preventive medicine in 2003, performed the first genomic exam in Plzeň in 2009, and visited the Mayo Clinic in 2018. He is a member of A4M, ACLM, ESNM and IFM — four of the leading international bodies for…
Languages: Czech
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Treatment highlights
- Pre-test physician consultation to clarify focus areas
- DNA SNP genotyping via Laboratoires REUNIS Luxembourg
+3 more items in What's included
Price on application — included within AI therapeutic programmes (from 19,000 CZK for the 6-month Basic programme). Standalone genomic consultation available; call +420 602 791 007 for an individual quote. Includes physician consultation + written report.