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 nameTest turnaround timePrice (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

Foetal gender testing from maternal blood (from 11 weeks of gestation)

10 working days 165

Single point mutation (carrier status) DNA test (for 1 person)

Individually 110 or NHS

Single point mutation (carrier status) DNA test (for 2 persons)

Individually 165 or NHS

Single point mutation (carrier status) DNA test (for 3 persons)

Individually 240 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

 

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