Qualified® test pricing

Qualified® test pricing

Why is prenatal testing important?

FAQ about prenatal testing 

Why Qualified® prenatal test?

  • The Qualified® test can be taken as early as the 10th week of pregnancy
  • The Qualified® test results are received within 3-5 business days from the day the sample is received by the laboratory

Qualified® 90°

Trisomies 21, 18, 13

Sex Aneuploidies*

560€

Qualified® 120°

Trisomies 21, 18, 13

Sex Aneuploidies*

DiGeorge syndrome

590€

Qualified® 180°

Trisomies 21, 18, 13

Sex Aneuploidies*

CNVs > 7mb**

690€

Qualified® 360°

Trisomies 21, 18, 13

Sex Aneuploidies*

CNVs > 7mb**

All other chromosomes

790€

Qualified® Plus

Trisomies 21, 18, 13, 9, 16

Sex Aneuploidies*

Microdeletions < 7mb (6 most common)***

RhSafe® (Rh factor)

690€

Qualified® KaryoPlus

Trisomies 21, 18, 13, 9, 16

Sex Aneuploidies**

Microdeletions < 7mb (9 most common)****

RhSafe® (Rh factor)

All other chromosomes

CNVs > 7mb**

990€

Qualified® Completa Plus

Trisomies 21, 18, 13, 9, 16

Sex Aneuploidies*

Microdeletions < 7mb (9 most common)****

RhSafe® (Rh factor)

All other chromosomes

CNVs > 7mb**

Hereditary genetic diseases

Non-heritable diseases

1.490€

Qualified® Full Risk

Trisomies 21, 18, 13, 9, 16

Sex Aneuploidies*

Microdeletions < 7mb (9 most common)****

RhSafe® (Rh factor)

All other chromosomes

CNVs > 7mb**

Hereditary genetic diseases

Non-heritable diseases

Genoma® Genescreen Focus for parents*****

1.690€

Qualified® prenatal test options for a twin pregnancy

Qualified® Twin Basic

Trisomies 21, 18, 13

520€

Qualified® Twin 360°

Trisomies 21, 18, 13

CNVs > 7mb**

All other chromosomes

790€

Qualified® Vanishing Twin

Trisomies 21, 18, 13

550€

SMA & CF test for pregnant women

SMA (Spinal Muscular Atrophy)

CF (Cystic Fibrosis)

99€

Qualified® prenatal test

  • The Qualified® prenatal test specificity is 99.9%
  • The Qualified® prenatal test error rate is only 0.1%
  • The Qualified® analyzes all 23 pairs of chromosomes and 512 regions of interest in the genome **
  • The most detailed analysis by the VeriSeq™ NIPT Solution v2 - illumina® platform

* The most common sex chromosome aneuploidies are as follows:

  • Turner syndrome (X0)
  • Triple X (XXX)
  • Klinefelter syndrome (XXY)
  • Jacobsen syndrome (XYY)

** The 180°, 360°, Karyo Plus, Completa Plus and Full Risk test options analyze 512 genomic regions of interest, identifying anomalies that, as per current databases, could involve CNVs (copy number variations)

*** 6 most common microdeletions < 7mb:

  • DiGeorge syndrome (22q11.2)
  • 1p36 deletion syndrome
  • Angelman syndrome (15q11.2)
  • Prader-Willi syndrome
  • Cri du Chat (5p- syndrome)
  • Wolf-Hirschhorn (4p- syndrome)

**** Additional 3 (to 6) microdeletions < 7mb:

  • Jacobsen syndrome (11q23-q24.3)
  • Langer-Giedion syndrome (8q24.11-q24.13)
  • Smith-Magenis syndrome (17p11.2)

***** Genoma® Genescreen Focus includes screening of 30 genes associated with over 31 hereditary genetic diseases

****** Initiative® is a preventive test for SMA types 1, 2, 3 and 4 (spinal muscular atrophy) and CF (cystic fibrosis) intended for pregnant women. The Initiative® SMA & CF test price is €190 The price for the Initiative® SMA & CF test with any of the Qualified® prenatal test options is €99

Determining the sex of the baby is included in every test option

Vanishing Twin is a unique option only for cases where the pregnancy starts as a twin pregnancy and continues as a singleton pregnancy

Qualified® prenatal tests can be paid for in full or in installments without interest.

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