Exploring genetic testing
Screen fertility genes now. Add embryo analysis later if you pursue IVF.
Free shipping
HSA/FSA eligible
Pay over time
Choose partner screening or an Embryo Report.
At-home cheek swab screening. No IVF or embryos needed.
Screen 750+ reproductive genes at home, with counseling included.
Choose checkout
One partner
$250
Both partners
$500
No reportable finding? Full refund. Available only when the completed report has no qualifying result under the published product terms.
Focused on infertility and recurrent loss
After your saliva samples reach the lab
Review findings with a genetic counselor
What happens next
From checkout to results, here’s what happens after you choose a plan.
Step 01
Choose one or both partners. We ship each person a saliva kit with everything needed to return it.
Step 02
After you send the kits back, the lab sequences and reviews reproductive genes.
Step 03
See findings in plain language, then talk them through with a genetic counselor and your care team.
Sample report
Preview partner findings, plain-language context, and a genetic counselor’s interpretation.
Guided sample report
Christina explains how to read the main finding, partner results, counselor context, and possible next steps.
Educational example only. Your results and next steps will depend on your history and care team.
Explore at your own pace
Partner results
Egg source
TUBB8
Related to egg maturation and early embryo development.
Also found: DHCR7 carrier result — a separate carrier-screening finding.
Sperm source
PLCZ1
May affect the sperm’s ability to activate the egg after fertilization.
Genetic counselor review
Reviewed by Christina, Genetic Counselor
Your report found a change in PLCZ1, a gene involved in sperm activation after fertilization. This result does not diagnose infertility, but it gives your care team a specific finding to review alongside your history and other testing.
A finding is information to discuss—not a prediction of whether you will conceive.
Your care team can use this information to discuss next steps with you.
What you can do next
Step 1 · Review your result
Meet with a reproductive genetics specialist or genetic counselor to review the evidence and discuss whether the finding fits your history.
Step 2 · Add clinical context
Bring prior fertility testing, treatment history, and family records so your care team can interpret the finding in context.
Step 3 · Explore your options
Ask whether testing a partner, reviewing carrier screening, or using future embryo data would add useful information.
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A positive panel is a starting point, not a verdict.
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Illustrative example. Your findings and recommendations will depend on your results and clinical history.
Infertility & Pregnancy Loss Panel
Understand what the panel tests, who it can help, what you receive, and what happens after your saliva kit reaches the lab.
For the Infertility & Pregnancy Loss Panel, Reticular mails you an at-home saliva kit and screens 750+ reproductive genes. You receive a personal report that explains any meaningful findings, their evidence and inheritance context, plus a conversation with a genetic counselor who helps you understand what to discuss with your care team.
The panel is designed for people planning a pregnancy, navigating unexplained infertility, or looking for more information after recurrent pregnancy loss. You do not need to be doing IVF, and you do not need existing embryo data to order it.
Testing both partners provides the most complete shared view because the report can consider each person's findings together. Testing one partner can still be a useful starting point. The panel costs $250 for one partner or $500 for both, and a genetic counselor can help you choose the option that fits your situation.
These tests look at different parts of the picture. Carrier screening usually asks whether partners could pass certain inherited conditions to a child, while a standard infertility evaluation may examine anatomy, hormones, semen, chromosomes, and other common factors. Reticular looks at individual genes connected to fertility, early embryo development, and pregnancy loss, adding a genetic layer those evaluations may not cover.
You can use the saliva panel before or during IVF to learn about reproductive-gene findings in one or both partners. If you already have compatible embryo sequencing data, Reticular also offers embryo reports that add pregnancy-loss, health-condition, and trait context without requiring a new embryo biopsy.
Yes. The relevant testing depends on whose egg and sperm will create the pregnancy and what screening has already been completed. Reticular can screen the intended genetic parent or parents, and a genetic counselor can help map the appropriate option to a donor or surrogacy plan.
If Reticular finds something meaningful, the report explains the gene, supporting evidence, and inheritance pattern. Your genetic counselor helps translate it into focused questions for your fertility clinician. Depending on the finding, your care team may discuss targeted testing, partner or family testing, IVF options, or other reproductive planning. The report supports those decisions; it is not itself a medical diagnosis or treatment plan.
A negative result means no reportable finding was identified within the genes and methods used by the panel. Your counselor can explain what was checked, what the result makes less likely, and which other parts of a fertility or recurrent-loss evaluation may still be useful.
We mail the kit to you, you collect the saliva sample at home, and you return it using the included materials. Results are typically ready about three weeks after the sample reaches the laboratory. Genetic counseling is included in the panel price.
Reticular encrypts genetic and personal information in transit and at rest, limits access to the people and systems working on your service, and does not sell your health information. You can request a copy or deletion of your data at any time.