Plan your family with knowledge, not surprises.
A simple carrier screening test for you and your partner that reveals what you might pass on to your child, so you can plan with calm and confidence. The price is per person, so each partner tests.
Built for people who want to get ahead.
You are planning a family or already expecting
You and your partner are related by blood
A genetic condition runs in either of your families
You have had a pregnancy loss or a child with a condition
You are planning IVF or using a donor
The problems it helps you solve.
Honest about what genetics can and can't do, focused on where it genuinely moves the needle.
Two healthy parents can still carry a hidden risk
Most of us carry hidden genetic changes and stay completely healthy. It only matters when both partners carry a change in the same gene, so it can pass quietly down a family tree unnoticed.
When you both carry it, it is 1 in 4 per pregnancy
If both partners carry a change in the same gene, every pregnancy has a one-in-four chance of an affected child. Knowing early turns an unknown into a number you can plan around.
Knowing early keeps every option open
Understand your options while every one is still open, and avoid difficult surprises later. It is one less unknown if you are considering IVF or other fertility support.
One sample each, for every pregnancy to come
You each test once. Your carrier status does not change, so a single screening informs this pregnancy and every one after it.
Insight you can actually act on.
Whether you and your partner carry a change in the same gene, the pairing that actually matters
Your chance of passing a recessive condition to a child, in plain language
Which options fit your result, from IVF with embryo selection to prenatal testing
That for most couples, screening simply brings welcome reassurance
Why a single test per person informs every pregnancy you plan
In your report
Hundreds of genes analysed for you
A clear High, Moderate or Average risk score
Clinically validated risk models
A doctor-ready PDF and a plain-language plan
Why it's worth doing now.
The outcomes that matter, not the science for its own sake.
See it early
Understand inherited risk years before symptoms, when prevention works best.
A plan that fits you
Turn results into specific, personal next steps, not generic advice.
Decide with your doctor
Guideline-backed findings you can share at your next appointment.
Insight for life
Your DNA doesn't change, so your report keeps paying off as science grows.
From order to insight, in four steps.
Order your test
Choose what you want to learn online in minutes. We ship a simple kit to your door.
Give a sample
A quick, painless sample at home. Seal it and mail it back in the prepaid kit.
Receive insights
Your encrypted, plain-language report lands in your secure dashboard in a few weeks.
Take action
A clear, personal plan you can act on, and share with your doctor when it counts.
A clear number, not a maybe.
Your report places you in one of three genetic-risk bands, with what each means and what to do next.
Average
Inherited risk in line with the general population. Stay on top of the basics and re-check as the science grows.
Moderate
A meaningful genetic tilt. Small, specific changes now compound into a very different decade ahead.
High
A strong inherited signal. The best time to act is well before any symptom appears.
Includes your full Carrier Screening report, a personal action plan, and a secure dashboard for life.
What's included
- Your Carrier Screening testClinical-grade DNA analysis
- Home sample pickup & dropA trained phlebotomist comes to you
- A plain-language reportYour result, with a personal action plan
- A free doctor consultationWalk through your result with a doctor, on us
A free consultation with a doctor.
Your result is never just a number. A qualified doctor walks you through what it means for you and your next steps, at no extra cost.
Good to know.
No. Most carriers are completely healthy and never know until it matters. It only affects the children you might have, and only if your partner carries a change in the same gene. A carrier result is not a barrier, it is knowledge that puts you in control.
Have questions before you decide?
Book a free 15-minute call with the team and we'll answer them, no pressure, so you can order with confidence.
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Your DNA won't change.
The decisions you make can.
The most personalized health plan you'll ever have is already inside you. Explore the tests and turn it into a longer, healthier life.