Prices of medical tests
Medical tests with the referral of the respective specialist are paid for by the NHS.
Tests are paid for by the NHS only if the patient has been to an NHS-paid visit and the medical specialist has issued a referral during the visit. List of specialists: geneticist, oncologist, oncologist-chemotherapist, haematologist, paediatric haematologist-oncologist, hepatologist, endocrinologist, gastroenterologist, infectiologist, gynaecologist, obstetrician, neurologist, immunologist, allergist, neurosurgeon, paediatrician, or radiology specialist. Only a urologist, andrologist or geneticist can refer to a state (NHS) paid “Y chromosome microdeletion DNA test.”
The accepted testing materials include both buccal swabs (saliva samples) and blood. For some tests (during pregnancy) we take blood samples.
The prices for medical tests do not include VAT (which does not apply to them), kinship and paternity prices include VAT, while the prices for other laboratory services do not (and are added to the final price).
Medical tests
| Test name | Test turnaround time | Price (EUR) |
DNA test for the risk of congenital breast and ovarian cancer in the BRCA1 gene | 10 working days | 100 or NHS |
One of the 4 most common mutations in the BRCA1 gene | 10 working days | 45 or NHS |
Celiac disease risk DNA test | 10 working days | 110 or NHS |
Haemochromatosis DNA test | 10 working days | 90 or NHS |
Haemochromatosis DNA test - Sequencing of the HFE gene | 10 working days | 420 or NHS |
Lactose intolerance DNA test in adults | 10 working days | 90 or NHS |
Thrombophilia DNA test | 10 working days | 110 or NHS |
One of the 5 variations included in the thrombophilia DNA test | 10 working days | 45 or NHS |
Thrombophilia — MTHFR gene variations | 10 working days | 50 or NHS |
DNA diagnosis of Gilbert's syndrome | 5 working days | 65 or NHS |
Detection of TPMT gene polymorphisms, predisposition to myelotoxicity of thiopurine drugs | 10 working days | 110 or NHS |
Testing for the most common mutation in CFTR gene | 10 working days | 90 or NHS |
Testing for the most common mutation causing Wilson's disease | 10 working days | 65 or NHS |
DNA test of the 5 most common variations of Crohn's disease | 10 working days | 110 or NHS |
IL28B DNA test for the efficacy of hepatitis C therapy with peginterferon (PEG-INF) and ribavirin | 10 working days | 80 or NHS |
Testing of the most common trisomies (13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy) Only for amniocentesis material sampled by medical personnel | 24-48 h | 155 or NHS |
Non-invasive prenatal test (NIPT) — NIPTIFY (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, microdeletions and other incidental findings. The test performs whole genome analysis. | 5-10 working days | 265 |
Non-invasive prenatal test (NIPT) — “Panorama” (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy | 12 working days | 390 |
Twin-pregnancy non-invasive prenatal test (NIPT) — “Panorama” (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy | 12 working days | 390 |
IVF-pregnancy non-invasive prenatal test (NIPT) — “Panorama” (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy | 12 working days | 390 |
Non-invasive prenatal test (NIPT) — “Panorama” (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy + 22q11.2 (DiGeorge syndrome) chromosome deletion | 12 working days | 475 |
Non-invasive prenatal test (NIPT) — “Panorama” (from 10 weeks of gestation) 13, 18, 21 chromosome trisomy, sex chromosome aneuploidy, triploidy + microdeletions: 22q11.2 (DiGeorge syndrome), 1p36 deletion syndrome, Angelman syndrome, Prader-Willi syndrome, Cri-du-chat syndrome | 12 working days | 525 |
Prenatal foetal rhesus factor (RhD) DNA test from maternal blood (from 11th week of gestation | 10 working days | 165 or NHS |
Foetal gender testing from maternal blood (from 11 weeks of gestation) | 10 working days | 165 or NHS |
Single point mutation (carrier status) DNA test | Individually | 110 or NHS |
Sample contamination DNA test (in the case of prenatal testing) | 5 working days | 110 |
Detection of DMD gene deletions by MLPA | 10 working days | 220 or NHS |
Alpha-1 antitrypsin deficiency DNA test (Pi-S and Pi-Z) | 10 working days | 55 or NHS |
Alpha-1 antitrypsin gene coding part testing | Individually | 220 |
Y chromosome most common microdeletion DNA test | 5 working days | 180 or NHS |
DNA test for Klinefelter, Turner, and Triple-X syndromes | 5 working days | 120 |