

Type
Blood Testing
Duration
1 hour
What's included
6 deliverables in this treatment
- Blood draw at MCP clinic for genomic analysis
- Next-generation sequencing through accredited lab partner
- Multi-domain risk report: metabolic, oncological, neurological, endocrine, cardiovascular, immunological
- High-penetrance variant identification (BRCA1/2, Lynch, arrhythmia genes, etc.)
- Physician interpretation consultation (MUDr. Růžičková + MUDr. Klubal)
- Personalised action plan with screening recommendations
MCP's whole-genome predictive screening provides a comprehensive map of your inherited disease risk across six major biological domains: metabolic, oncological, neurological, endocrine, cardiovascular, and immunological. The analysis is performed through MCP's accredited genomic lab partners and interpreted by MUDr. Silvie Růžičková (genetics) and MUDr. Radek Klubal. Unlike direct-to-consumer ancestry tests, this is a clinically framed risk assessment with actionable recommendations for screening frequency, lifestyle modification, and preventive intervention.
About this treatment
Predictive genomic medicine is changing how proactive individuals approach long-term health. MCP's whole-genome screening programme is designed for patients who want a comprehensive picture of their inherited disease predispositions — not just ancestry data, but clinically interpreted risk information that drives real preventive decisions.
The analysis is performed through MCP's specialist genomic laboratory partners using next-generation sequencing (NGS) technology. Blood is drawn at the Praha 4 clinic by MCP's nursing team, processed through the accredited partner lab network, and the interpreted results are delivered in a structured physician consultation.
Domains covered in the report:
Good to know
- Sequencing method
- NGS via accredited partner lab
- Domains
- 6: metabolic, oncological, neurological, endocrine, cardiovascular, immunological
- Genetics lead
- MUDr. Silvie Růžičková
- Report type
- Pathogenic variants + polygenic risk scores
Who is this for?
Health-conscious individuals 30–55 years old, family history of hereditary cancer or cardiovascular disease, anyone wanting a comprehensive genetic risk baseline
Preparation required
Book consultation first via extranet.mc-praha.cz to discuss scope and confirm pricing. No fasting required for blood draw. Results typically take 3–6 weeks via sequencing lab. Return appointment booked at time of draw.
About the clinic
Reviews, team and credentials
Independent review links and clinic-reported team information.
Clinical team
MUDr. Radek Klubal (founder, managing director, clinical immunologist) leads a team that includes MUDr. Silvie Růžičková (clinical genetics, reproductive medicine), MUDr. Barbora Klubalová (venereology, dermatology), Ing. Silvia Illýová (nutritional counsellor, BSc Human Nutrition, SPU Nitra), and Pavla Schubertová, Dis. (head nurse). All physicians hold Czech specialist licences in their respective fields.
Languages: cs, en
Treatment highlights
- Blood draw at MCP clinic for genomic analysis
- Next-generation sequencing through accredited lab partner
+4 more items in What's included
From 25,000 Kč for comprehensive genomic analysis. Price confirmed at booking. Includes blood collection, genomic sequencing via accredited lab partner, and physician-led interpretation session. Multi-domain report covering metabolic, oncological, neurological, endocrine, cardiovascular, and immunological risk.
