Genetic Check-up

A genetic check-up does not mean 'a disease is definitely present'; most often it indicates a 'risk' or a 'predisposition'. The risk may be high yet the disease may never develop; the risk may be low and the disease may still occur. For this reason, results are interpreted not on their own but together with clinical evaluation, family history, lifestyle and laboratory–imaging findings.

• Cancer predisposition assessment (breast, ovarian, colon, prostate, etc.)
• Cardiovascular disease risk analysis
• Screening for clotting (thrombosis) disorders
• Pharmacogenetics — assessing which drug will be more effective or more likely to cause side effects in the person
• Determining the tendency toward obesity and metabolism
• Sports performance and muscle structure analysis
• Longevity / healthy aging assessments
• Detecting carrier status for rare hereditary diseases
• Family planning — carrier screening before having children

1. 1

   Sample Collection

   A blood sample or saliva sample is taken under sterile conditions; the procedure is short and does not affect daily life.

2. 2

   Laboratory DNA Analysis

   DNA analysis is carried out in an accredited laboratory; reporting may take a few weeks depending on the scope of the panel examined.

3. 3

   Geneticist's Interpretation

   The results are evaluated by a genetics specialist; risks and predispositions are reported in a clear, understandable way.

4. 4

   Personalized Health Plan

   Findings are combined with clinical evaluation, family history and lifestyle and turned into an early-precaution and follow-up plan.

Genetic check-up sampling is not an invasive procedure; the patient continues daily life the same day.