Thrombophilia & NAIT Panel
Targeted genetic variant analysis
A targeted genetic panel that screens for inherited thrombophilia and platelet antigen variants associated with recurrent pregnancy loss, thrombotic risk, and neonatal alloimmune thrombocytopenia (NAIT).
€299.00
per test kit
ISO 9001:2015 Certified
GDPR Compliant
Free Shipping
What's Included
Full Description
The Thrombophilia & NAIT Panel analyses selected genetic variants associated with inherited thrombophilia, recurrent pregnancy loss, thrombotic events, and neonatal alloimmune thrombocytopenia. The panel includes variants in genes involved in coagulation, platelet antigens, folate metabolism, fibrinolysis, lipid metabolism, and the renin-angiotensin pathway.
This panel may be useful for couples or individuals with more than one miscarriage, individuals with recurrent or early-onset thrombotic events, those with a strong family history of thrombosis, and neonates with thrombocytopenia or unexplained thrombosis. Results should always be interpreted in the appropriate clinical and genetic context by a healthcare professional.
The Process: from purchase to results
- Order your test – The kit is delivered discreetly to your door. Once you purchase your test kit, you will receive an email with a link to the Customer Guide.
- Fill in the form – Submit the online consent form and medical history questionnaire.
- Collect your sample – Collect buccal swab samples following the instructions provided.
- Send it back – Return your sample using the mailing bag with prepaid return shipping label.
- Receive your report – Get your genetic thrombophilia and NAIT results within approximately 25 working days after sample receipt.
Optional Add-Ons/Related Tests
Genetic Fertility & Vaginal Microbiome
Genetic Carrier Screening Test
Key Features
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Screens 22 genetic variants in 17 genes linked to thrombophilia and NAIT
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Can support investigation of recurrent pregnancy loss, thrombosis risk, neonatal thrombocytopenia, or unexplained neonatal thrombosis
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Available as a stand-alone panel or as an add-on to Female or Male Infertility Panels
Frequently Asked Questions
Why should I get this test?
This test may help identify inherited genetic variants that increase the risk of thrombosis, recurrent pregnancy loss, or neonatal alloimmune thrombocytopenia. The results may support personalised clinical management when assessed together with your medical and family history.
Who could benefit from this test?
The panel may be considered for couples or individuals with recurrent pregnancy loss, individuals with recurrent or early-onset thrombosis, individuals with a strong family history of thrombotic events, and neonates with thrombocytopenia or unexplained thrombosis.
How do I prepare for sample collection?
Do not smoke, eat, drink anything except water, brush your teeth, or chew gum for 60 minutes before buccal swab collection. Collect the sample immediately after opening the swab package and follow the labelling, collection, and transport instructions carefully.
What is included in the report?
Your report includes the detected genotype for the tested thrombophilia and NAIT-associated variants, together with interpretation to support discussion with your healthcare provider.
How do I interpret the results?
Results should be reviewed with your doctor, haematologist, gynaecologist, or genetic healthcare professional. Interpretation should take into account your personal history, family history, pregnancy history, and any relevant clinical findings.
Do you ship worldwide?
This service is currently available only for customers living in the EU.
