Genetic Testing in Prague

A genetic test detecting inherited thrombophilia (clotting-risk) mutations — relevant before pregnancy, hormone therapy or surgery, or with a family history of clots. Self-pay, no referral, results delivered electronically.

Initial consultation with genetic specialist to discuss testing options.

Consultation with results interpretation and diagnosis discussion.

A celiac-disease genetic test through LABSHOP analysing HLA-DQ predisposition markers to assess genetic risk of celiac disease. Order online and collect the sample at a SPADIA point in Prague.

Sperm DNA fragmentation test for male fertility assessment.

Evaluation of chromosome aberrations in peripheral blood.

Cytogenetic analysis of chromosomes from blood sample.

Measure biological age through telomere analysis.

Non-invasive prenatal genetic screening test from maternal blood.

Genetic testing for hereditary breast and ovarian cancer predisposition.

Galen Clinic's oncogenetic testing analyses genes linked to an increased risk of the most common hereditary cancers, including the high-risk BRCA1 and BRCA2 genes. The panel covers genes associated with elevated risk of breast, ovarian, prostate, colorectal, pancreatic, kidney, skin and other cancers. The test is performed from a simple blood sample taken during a standard clinic visit and sent to a specialised genetics laboratory, with results typically available within about a month. Because a result can carry significant personal and family implications, testing is always preceded by a physician consultation to choose the right test and explain what the results mean; any clinically significant finding is interpreted together with a clinical geneticist. The aim is not to diagnose existing disease but to inform a personalised, better-targeted prevention and monitoring plan.

EliteMedical offers DNA health testing that analyses 47 genes organised across eight preventive health categories: oxidative stress and antioxidant capacity, detoxification ability, inflammation predisposition, methylation and gene expression regulation, lipid and cholesterol metabolism, bone health, insulin sensitivity, and vitamin metabolism (vitamins A, D, C, and B12). The test is performed from a simple saliva or blood sample and results are interpreted in Czech by an EliteMedical physician or health specialist, with personalised recommendations covering diet, supplementation, and lifestyle adjustments based on the patient's specific genetic variants. Unlike diagnostic genetic tests for monogenic diseases, this test focuses on polygenic health trait variants — the kind that influence susceptibility and response to lifestyle interventions. It is particularly valuable for people with a strong family history of chronic disease (cardiovascular, metabolic, bone, or inflammatory conditions) who want to understand their personal risk landscape before symptoms emerge.