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NIPTtest - NIFTY
NIPTtest - NIFTY
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NIPTTEST

Swedens most advanced NIPT-test

Available in Stockholm and Gothenburg.

Experience risk‐free NIPT testing with NIFTY & NIFTY Pro—over 99% accuracy for common and rare chromosomal abnormalities. Choose NIFTY for comprehensive screening or NIFTY Pro for detailed analysis. Available from week 10.

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The prenatal test with most markers

Bock NIPT

Sweden's most advanced prenatal test

Bock NIPT

Risk-Free with blood sample from mother

Nifty - NIPT TEST
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Trisomy 21 - Down Syndrome, trisomy 18 - Edwards syndrome, trisomy 13 - Pataus syndrome

Four Sex Abnormalities

Three Rare Autosomal Trisomies

Determine Gender - Optional

4490 SEK 

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Nifty PRO - NIPT TEST
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The most Comprehensive NIPT Test in Sweden

Includes everything from Nifty Basic

92+ different microdeletions
including Cri-du-chat syndrome, 1p36, 2q33.1, Prader-Willi/Angelman syndrome, DiGeorge syndrome (22q11.2) and 16p12.2-p11.2 

Incidental Findings

6990 SEK 

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Mobile sampling; We come to you.

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We'll come to you

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6 days a week

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Quick and smooth

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Safe

With Nifty and Qura, you get access to safe and convenient prenatal diagnostics through mobile sampling in Stockholm and Gothenburg. Choose to take your NIPT test wherever it suits you – at home, at your workplace, or another convenient location.

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FAQ
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What can i expect?

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Non invasive


Nifty is a non-invasive prenatal test with no risk of miscarriage. The test requires only a venous blood sample from the mother.

Early screening


The test can be performed as early as pregnancy week 10+0, providing you with early and reliable information about your baby's health.

Comprehensive screening


Nifty provides a complete screening for chromosomal abnormalities, including T21, T18, and T13, covering all 23 chromosome pairs for a thorough overview of your baby's health.

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High accuracy


With a sensitivity of over 99% for T21, T18, and T13, Nifty offers exceptionally high accuracy and reliability, based on a study of 147,000 pregnancies.

Fast results


Fast and Easy. After our team collects a blood sample, the results are delivered digitally within 5-8 days.

Reliable


Over 15,000,000 tests have been conducted by clinics worldwide, making Nifty one of the most trusted prenatal tests/NIPT tests.

Certified laboratorium


Our analyses are conducted in ISO-certified laboratories in Denmark, ensuring the highest standards and patient safety.

ISO 13485

ISO 15189

ISO 27001

BS 10012

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Betalningsalternativ
Betalningsalternativ klarna
Betalningsalternativ mobil


With us, payment is simple and secure.


We use Zettle by PayPal, allowing us to accept major credit cards and Swish for quick and seamless transactions. For those who prefer extra flexibility, we also offer installment options via Klarna.


You pay nothing until the sampling appointment, ensuring that you feel completely secure and can focus on receiving the best possible service. Our goal is to make the entire process as smooth and convenient as possible for you!


Nifty vs Nifty PRO

Comparison of NIFTY and NIFTY PRO

Comparison between NIFTY and NIFTY PRO

Category NIFTY NIFTY PRO
Basic Test
Screening for trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome). 		Yes Yes
Sex Chromosomal Aneuploidies
Tests for sex chromosome abnormalities, including Turner syndrome, Klinefelter syndrome, and Jacob's syndrome (XXY). 		Yes Yes
Extended Tests (92+ Chromosomal Abnormalities)
Tests for more than 92 different chromosomal abnormalities, including microdeletions and sex chromosome abnormalities. 		No Yes
Genetic Microdeletions
Detects 7 microdeletions, including DiGeorge syndrome, 1p36 deletion syndrome, Prader-Willi syndrome, and Angelman syndrome. 		No Yes
Gender Determination
Find out the baby's gender with high precision if desired. 		Yes Yes
Total Number of Markers
Number of genetic markers analyzed to detect chromosomal abnormalities. 		10+ (Trisomies and Sex Chromosome Abnormalities) 102+ (Including Sex Chromosome Abnormalities and Microdeletions)
Time for Results
Delivery time. 		Within 5–7 business days Within 5–8 business days
cfDNA Technology
The test uses non-invasive cfDNA technology for safe screening, without risk of miscarriage. 		Yes Yes
Precision
Over 99% accuracy for detected chromosomal abnormalities. 		Yes Yes
From Week 10
Both tests can be performed early in pregnancy, starting from week 10. 		Yes Yes
  • Individuals who have recently undergone a blood transfusion, organ transplant, immunotherapy, or stem cell therapy may have affected test results and should avoid the test.
  • Individuals with specific chromosomal abnormalities such as chromosome polyploidy (e.g., triploid or tetraploid), balanced chromosome translocation, inversion, or other complex chromosomal abnormalities.
  • Pregnancies with mosaicism.
  • Blood-thinning medications: Have undergone heparin treatment or similar within the last 24 hours.
  • Individuals with genetic or biological conditions such as uniparental disomy or other specific genetic disorders that may affect test reliability.
  • Individuals who have had a miscarriage within the last 8 weeks.
  • If you are earlier than pregnancy week 10.
  • Provide Last Menstrual Period: Enter your last menstrual period or estimated due date according to a previous ultrasound when booking.
  • NIPT: NIPT can be performed from pregnancy week 10+0. Before this, the blood sample cannot be analyzed. If you have a long menstrual cycle or do not remember your last period date, we recommend booking the NIFTY test around pregnancy week 11 to avoid rescheduling and additional costs.
  • Ultrasound Before Testing: It is recommended to have an ultrasound before taking the test. The ultrasound helps ensure that the pregnancy week is correct and is also essential for detecting multiple pregnancies (twins or more). Additionally, the ultrasound confirms the fetal heartbeat and overall health, providing extra reassurance before taking the NIFTY test.
  • Fasting Not Required: The NIFTY test does not require fasting. You can eat and drink as usual before taking the blood sample.
Nifty PRO NIPT resultat
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Compare Nifty & Nifty Pro with other NIPT in Sweden

Comparison of NIFTY, NIFTY PRO and Other Tests
Category NIFTY NIFTY PRO Babyscreen Lifegenomics
Basic Test
Screening for trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome). 		Yes Yes Yes Yes
Sex Chromosomal Aneuploidies
Tests for sex chromosome abnormalities, including Turner syndrome, Klinefelter syndrome, and Jacob's syndrome. 		Yes Yes No No
Extended Tests
Tests for additional chromosomal abnormalities, including microdeletions and sex chromosome abnormalities. 		No 92+ Chromosomal Abnormalities No 80+ Chromosomal Abnormalities
Genetic Microdeletions
Detects 7 microdeletions, including DiGeorge syndrome, 1p36 deletion syndrome, Prader-Willi syndrome, and Angelman syndrome. 		No Yes No Yes
Gender Determination
Determine the baby's gender with high precision if desired. 		Yes Yes Yes Yes
Total Number of Markers
Number of genetic markers analyzed to detect chromosomal abnormalities. 		10+ (Trisomies and Sex Chromosome Abnormalities) 102+ (Including Sex Chromosome Abnormalities and Microdeletions) 3 85+ (Including Sex Chromosome Abnormalities and Microdeletions, when purchasing the extended test)
Time for Results
Delivery time. 		Within 5–7 business days Within 5–8 business days Within 7–12 business days Within 5–9 business days
cfDNA Technology
The test uses non-invasive cfDNA technology for safe screening, without risk of miscarriage. 		Yes Yes Yes Yes
Precision
The tests have over 99% accuracy for detected chromosomal abnormalities. 		Yes Yes Yes Yes
False Positives
Incorrect positive results, stated as a percentage. 		Less than 0.098% Less than 0.098% 0.1% 0.08%
Number of Publications
Number of scientific publications related to the test. 		90+ publications 90+ publications N/A N/A

What is a NIPT-test?

A NIPT test (Non-Invasive Prenatal Test) is a non-invasive prenatal screening that analyzes fetal DNA through a simple blood sample from the pregnant woman. This test can be performed as early as the 10th week of pregnancy and carries no risk of miscarriage.


NIPT is used to detect chromosomal abnormalities in the fetus, such as:

  • Down syndrome (Trisomy 21)
  • Edwards syndrome (Trisomy 18)
  • Patau syndrome (Trisomy 13)

One of the most advanced NIPT tests available is the Nifty test, which provides high accuracy (over 99%) for detecting these trisomies. Results are typically available within 5–8 days after the blood sample is taken. Additionally, the Nifty test analyzes all 23 chromosome pairs to offer a comprehensive overview of the fetus's genetic health.

For those seeking even more detailed screening, Nifty PRO includes everything from the standard Nifty test plus screening for over 92 different microdeletions, including:

  • Cri-du-chat syndrome
  • 1p36 deletion syndrome
  • DiGeorge syndrome (22q11.2 deletion syndrome)

In summary, NIPT tests like Nifty and Nifty PRO provide a safe, early, and highly reliable method for obtaining essential genetic health information about your baby during pregnancy.

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Niftytest.se is operated by Qura Sweden AB, a leader in mobile sampling in Sweden, primarily in Stockholm and Gothenburg.

As the exclusive distributor of NIFTY and NIFTY Pro in collaboration with BGI, we offer advanced and reliable prenatal diagnostics.

Our service is simple, safe, and non-invasive, with fast on-site sampling – available for both individuals and healthcare providers.

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