One partner
$250
After pregnancy loss
Catch causes of pregnancy loss.
Affordable genetic testing from $23/mo†. Get answers with confidence, risk-free.
Infertility & Pregnancy Loss Panel
Screen 750+ reproductive genes at home, with counseling included.
Choose checkout
Both partners
$500
Results are informational and do not diagnose a condition, explain every pregnancy loss, recommend treatment, or guarantee an outcome.
Payment options through Affirm are subject to eligibility and may require a down payment.
No-Finding Promise
No reportable finding? Full refund.
Available only when the completed report has no qualifying result under the published product terms. Request during your included results call.
Eligibility termsat-home saliva sample
No clinic visit required
Results in about 3 weeks
After samples reach the lab
Counseling included
Review findings with a counselor
What happens next
How the panel works
From checkout to results, here’s what happens after you choose a plan.
Step 01
Test at home
Choose one or both partners. We ship each person a saliva kit with everything needed to return it.
Step 02
We screen the results
After you send the kits back, the lab sequences and reviews reproductive genes.
Step 03
We explain your report
See findings in plain language, then talk them through with a genetic counselor and your care team.
How Reticular can help
See how a counselor turns a dense report into a conversation.
Christina walks through an illustrative report, explains where to begin, and separates the main finding from supporting context and possible next steps.
2:10
Guided sample report
A genetic counselor walks through a 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.
Read the walkthrough summary
- Start with the report summary: it highlights the findings most relevant to the couple’s history without treating them as a diagnosis.
- Compare each partner’s results, then open an individual finding to see the evidence, inheritance pattern, and plain-language interpretation.
- Use Christina’s counselor note to separate the result that may help explain the losses from lower-risk carrier information.
- Bring the result and suggested next steps to a reproductive genetics specialist or genetic counselor for decisions specific to your history.
Sample report
See what the report includes—and what it does not claim.
Explore illustrative findings, inheritance context, and a counselor’s interpretation. The report informs a conversation—it does not diagnose or predict.
Explore at your own pace
Explore the sample yourself
Partner results
Maya
Higher riskEgg source
TUBB8
May help explain repeated early losses.
Also found: DHCR7 carrier result — lower relevance to the losses.
Daniel
Moderate concernSperm source
PLCZ1
May affect the sperm’s ability to activate the egg after fertilization.
Genetic counselor review
Christina's counselor note
Reviewed by Christina, Genetic Counselor
Your report found a change in TUBB8, a gene that helps eggs mature and supports the embryo’s earliest development. Findings like this can sometimes help explain repeated early losses that standard chromosome testing misses.
Nothing about how you tried to conceive caused these losses.
Your care team can use this information to discuss next steps with you.
What the panel screens
750+
genes
Grouped by what each gene does in reproduction.
Egg maturation & division
96 genesTUBB8 · PATL2
Fertilization
34 genesWEE2 · PLCZ1
Early embryo development
52 genesBTG4 · PADI6
Molar pregnancy
14 genesNLRP7 · KHDC3L
Embryo survival & growth
386 genesCPLANE1 · DYNC2H1
Pregnancy support
22 genesF5 · SERPINC1
Sperm development & function
154 genesCFTR · AURKC
Representative groups and genes from the full panel.
1 of 3
View the complete sample report (opens in a new tab)
Illustrative example. Your findings and recommendations will depend on your results and clinical history.
Evidence and boundaries
Know what question each test answers.
Reticular's reviewed patient resources explain how reproductive-gene screening differs from chromosome testing, carrier screening, and the broader recurrent-loss evaluation.
Common questions
It screens one or both intended parents across 750+ genes associated with fertility, early embryo development, and recurrent pregnancy loss. It analyzes a saliva sample from the parent or parents, not an embryo or a prior pregnancy.
Not in every case. A well-supported finding may identify a reproductive-gene factor worth discussing with your care team, but the panel does not explain most individual losses, diagnose a cause, or predict whether a future pregnancy will succeed.
A karyotype examines chromosome number and structure. Carrier screening primarily asks whether a future child could inherit certain conditions. This panel examines individual reproductive genes associated with fertility and pregnancy viability, so the tests answer different questions and may be used alongside one another.
No. The panel does not replace pregnancy-tissue testing, parental karyotyping, carrier screening, or evaluation of uterine, hormonal, clotting, immune, and other possible contributors to recurrent loss.
Either option is available. Screening both partners provides a combined view of each person’s reproductive-gene findings. A genetic counselor can help you decide which option fits your history and any testing you have already completed.
A negative result means the panel did not identify a reportable finding under its current methods and evidence standards. It does not rule out every genetic factor or other possible reason for infertility or pregnancy loss.
Yes. A genetic counselor helps place the report in context, explains what a finding does and does not mean, and helps you prepare questions for your fertility clinician or other care team.
A human next step
Questions? Get a real answer from Reticular.
Text our team for a quick product question, or book a complimentary conversation with Christina, our licensed genetic counselor, to discuss your history, prior testing, and whether one- or two-partner screening fits.
Already have embryo data?
Reticular also offers embryo reports that use compatible PGT-A data you already have, with no new embryo biopsy.