Comprehensive Premarital Genetic Compatibility Test
Whole exome sequencing for both partners, covering 20,000+ genes and 4,000+ genetic conditions — reviewed by 3 specialist physicians.
Powered by Whole Exome Sequencing (WES) on NGS
Your sample is analyzed by Whole Exome Sequencing (WES) on a next-generation sequencing (NGS) platform — reading the ~20,000 protein-coding genes where the vast majority of known disease-causing variants are found. Results are interpreted against 4,000+ scientifically described inherited conditions and reviewed by 3 specialist physicians.
The medical terms, but in everyday language
The words you'll hear most in genetic testing, explained simply and directly — so you enter the experience already understanding what's what.
Genetic compatibility
Comparing both partners' DNA to see if there are silent variants that only matter when they meet in the same gene.
Carrier
A perfectly healthy person who quietly carries one copy of a genetic change. Being a carrier does not mean you're sick.
Variant / mutation
A small change in the DNA text. Many variants are harmless — we only flag the ones with known medical meaning.
DNA
The instruction manual inside your cells. We read the medically-relevant parts of yours to build the report.
Exome
The ~1% of your DNA that actually gives instructions to build proteins — where most known disease-causing changes live.
Whole Exome Sequencing (WES)
Reading that entire ~1% end-to-end — roughly 20,000 genes — instead of only a small pre-picked list.
Whole Genome Sequencing (WGS)
Reading everything — the exome plus the rest of the DNA around it. Available on request when you want the widest possible net.
Next-Generation Sequencing (NGS)
The modern lab technology we use to read millions of DNA letters accurately and in parallel.
Recessive condition
A condition that only shows up when a child inherits the same change from both parents.
Results / clarity
A plain-language report explained by a specialist — so you understand what it means for you, not just what it says.
These are simplified summaries to help you follow along — they don't replace direct medical consultation with a specialist.
Why this test matters
Marriage is a big beginning. Genetic knowledge beforehand helps you make clearer, more informed decisions — not to cause worry, but to turn data into practical understanding.
What the test is
An advanced genetic screen using whole exome sequencing for both partners, interpreted as a couple to reveal inherited risks before starting a family.
Why healthy couples can still carry risk
Some conditions travel silently. A healthy person can carry a variant that becomes relevant only when both partners carry a change in the same gene.
What the test can help identify
Covers 20,000+ genes and 4,000+ scientifically known genetic conditions and variants, and highlights shared couple-level risk.
What happens after results
A clear explanation and post-result support for your questions, plus a compatibility package that arrives after your results.
What the test includes
Everything from sample collection to final report — one package covering both partners.
- Whole exome sequencing for both partners
- Analysis of 20,000+ genes
- Coverage of 4,000+ scientifically known genetic conditions and variants
- Simple blood sample collection from both partners — inner side of the elbow
- Next-generation sequencing (NGS) analysis
- Results reviewed by 3 specialist physicians
- Comprehensive individual report for each partner
- Couple compatibility report
- Post-result support for your questions
- Compatibility package delivered after results
From order to compatibility package
- 1
Choose your package
Pick the Individual test or the Couple package — a NAWA specialist contacts you within 24 hours to confirm your details.
- 2
We come to you for sample collection
A trained nurse visits you at home or your preferred location, 7 days a week. A simple blood sample is taken from the inner side of the elbow.
- 3
Receive your report and counseling
Get your clear, couple-focused report within 45–50 business days, plus a bilingual counseling session and follow-up support.
Clear reports, specialist review
- Individual report per partnerRelevant genetic findings within the test scope.
- Couple compatibility reportHighlights any shared genetic risks between partners.
- Specialist medical reviewReviewed by 3 specialist physicians.
- Plain-language explanationResults explained without medical jargon.
- Post-result supportGuidance for your questions and next-step decisions.
- Compatibility packageIncludes the warranty booklet and a special gift.
Our commitment to you
Warranty up to 10,000 SAR
If a genetic condition within the test scope is missed, subject to the terms, conditions, and coverage scope.
Full immediate refund
If the expected delivery time for results is exceeded, subject to terms and conditions.
Who this test is for
Important notes before ordering
- This test is not a substitute for direct medical consultation when needed.
- Results depend on the coverage and analysis in effect at the time the report is issued.
- Certain conditions or variants may fall outside the exome — Whole Genome Sequencing (WGS) is available on request for broader coverage.
- Terms, conditions, and coverage scope apply to the warranty and refund.
Pick the package that fits your journey
Individual Genetic Test
- Comprehensive carrier panel
- Personal genetic risk report
- Result explanation with a specialist
- Confidential handling of your data
Once in a lifetime · Covered by NAWA warranty · Joint reports
Start your NAWA journey
Guided from booking to results