Wherever you are in your family planning journey, carrier screening fits.
Whether you're trying naturally, planning an IVF cycle, or planning to use a donor. Carrier screening empowers you with information to make confident pregnancy decisions.
You can be healthy, have no family history, and still carry a gene variant that could affect your children
Carrier screening looks at shared reproductive risk, not your own health. Planning a pregnancy, IVF, or donor conception with this knowledge means you're prepared whatever the result.
90%
of couples who have a child with a serious inherited condition had no family history beforehand. Knowing is the difference.
80%
of people carry at least one genetic condition. Being a carrier is common and it doesn't affect your own health.
780+ genes
screened for serious childhood conditions, so you have the most complete and actionable information.
What test is for you
3 genes or 780+? Here's what the difference actually means
The Medicare-funded test covers 3 genes and misses ~70% of at-risk couples. At Eugene we want you to have options without overwhelming you with choice - so you can make the right call for your family.
-
Screens 780+ genes for hundreds of conditions.
-
Our most thorough test that identifies ~90% of at-risk couples.
-
Includes CF, SMA and FXS plus many more.
-
Covers conditions relevant to all ethnic backgrounds.
-
Reports your individual carrier status for every condition.
-
Flags conditions that may be relevant to your own health.
$1499 for couples. $949 for individual.
This is for you if
- Taking the next step into pregnancy knowing you've done everything you can.
- You're doing IVF or using a donor and need results before your next step.
- If you want your own individual results, as well as a combined report.
- You have mixed ancestry and want the broadest possible coverage.
-
Screens 620+ genes focused on serious childhood conditions.
-
Identifies approximately 80% of at-risk couples.
-
Includes CF, SMA and FXS plus many more.
-
Covers conditions relevant to all ethnic backgrounds.
-
Reports your combined reproductive risk (low or increased).
-
Individual CF, SMA and FXS results provided for the female partner.
*Medicare eligibility required to purchase.
This is for you if
- You and your partner want to understand your shared risk together.
- You'd prefer one combined result rather than individual carrier status.
- You're not on an timeline and turnaround isn't critical.
- The Medicare rebate matters to your decision.
-
Screens for the 3 common inherited conditions. CF, SMA and FXS
-
10-20% of at-risk couples will be identified by this test. Depending on your family background.
-
Female-first approach. If you're a carrier, your partner can then be tested
*Medicare eligibility required. Full price $399.
This is for you if
- You've been offered the Medicare-funded test and want to do it from home. Rebate can only be claimed once.
- You want a starting point before deciding whether to go further.
- You're in your first trimester and need a quick, guideline-level screen.
How it works
Four simple steps, expert analysis, and a personalised plan for your long-term wellness.
-
Order your test
Start your journey from the comfort of home
-
Share your story
Tell us about your family planning goals so we can personalise your experience
-
At-home collection
Simply swab your cheek and return your kit via prepaid package
-
Review and guidance
Get a personal report, genetic telehealth consult and next steps
