Reticular

Exploring genetic testing

Start with genetics now.

Screen fertility genes now. Add embryo analysis later if you pursue IVF.

Reticular at-home saliva sequencing kit for two partners
  • Free shipping

  • HSA/FSA eligible

  • Pay over time

What the panel includes

  1. 01

    750+ reproductive genes

    Focused on infertility and recurrent loss

  2. 02

    Results in about 3 weeks

    After your saliva samples reach the lab

  3. 03

    Counseling included

    Review findings with a genetic counselor

What happens next

How the panel works

From checkout to results, here’s what happens after you choose a plan.

  1. Step 01

    Test at home

    Choose one or both partners. We ship each person a saliva kit with everything needed to return it.

    Reticular test kit, papers, and sample vial.
  2. Step 02

    We screen the results

    After you send the kits back, the lab sequences and reviews reproductive genes.

    Illustrated genomic analysis chart.
  3. Step 03

    We explain your report

    See findings in plain language, then talk them through with a genetic counselor and your care team.

    Genetic counselor explaining a report.

All products

Choose what fits your next step.

Start with your recommendation, or explore options for trying to conceive and IVF.

Choose your path

Screen yourself or your partner. No embryos or IVF needed — just a simple saliva kit.

Infertility & Pregnancy Loss Panel

For anyone trying to conceive

$250one partner · $500 for both

Screen 750+ genes tied to infertility and recurrent pregnancy loss. No IVF or embryos required.

Watch a 2-minute pregnancy-loss report walkthrough
  • 750+ reproductive genes
  • Simple at-home saliva kit
  • Genetic counseling included
No embryos or IVF needed — only a saliva sample.

Choose checkout

One partner

$250

Both partners

$500

Want to talk it through first?

Ask a real person what each option includes and which may fit your situation.

Sample report

See what a reproductive-gene report looks like

Preview partner findings, plain-language context, and a genetic counselor’s interpretation.

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
  1. Start with the report summary: it highlights the findings most relevant to the couple’s history without treating them as a diagnosis.
  2. Compare each partner’s results, then open an individual finding to see the evidence, inheritance pattern, and plain-language interpretation.
  3. Use Christina’s counselor note to separate the result that may help explain the losses from lower-risk carrier information.
  4. Bring the result and suggested next steps to a reproductive genetics specialist or genetic counselor for decisions specific to your history.

Explore at your own pace

Explore the sample yourself

Partner results

Maya

Review finding

Egg source

TUBB8

Related to egg maturation and early embryo development.

Also found: DHCR7 carrier result — a separate carrier-screening finding.

Daniel

Review finding

Sperm source

PLCZ1

May affect the sperm’s ability to activate the egg after fertilization.

Genetic counselor review

Christina, Genetic Counselor

Christina's counselor note

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

Parent resting beside a sleeping baby

Step 1 · Review your result

Review the finding with a specialist

Meet with a reproductive genetics specialist or genetic counselor to review the evidence and discuss whether the finding fits your history.

Adult hands gently holding a newborn's foot

Step 2 · Add clinical context

Compare it with your clinical history

Bring prior fertility testing, treatment history, and family records so your care team can interpret the finding in context.

Parent holding a baby at home

Step 3 · Explore your options

Decide whether more testing adds context

Ask whether testing a partner, reviewing carrier screening, or using future embryo data would add useful information.

1 of 3

Speak with a specialist (opens in a new tab)

A positive panel is a starting point, not a verdict.

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View the complete sample report (opens in a new tab)

Illustrative example. Your findings and recommendations will depend on your results and clinical history.

Find your Reticular plan | Reticular