After PGT-A
Use the PGT-A data you already have to screen every embryo for 24+ health conditions and the genes behind pregnancy loss—without another biopsy.
We confirm your data is compatible before you pay
One flat fee for every embryo you have across every cycle.
$1,000
No reportable finding? Full refund. Available only when the completed report has no qualifying result under the published product terms.
Results do not diagnose a condition, predict whether a child will develop one, or guarantee an outcome.
Payment options through Affirm are subject to eligibility and may require a down payment.
No new biopsy
Counselor review
Pay over time
Your PGT-A report answers one question — chromosomes. Both Reports read that same data for more.
Pregnancy loss only
$750
Pregnancy loss + health
$1,000
What happens next
No new biopsy, and a counselor walks you through the result.
Step 01
We ship two saliva kits to screen you both across 750+ genes, and send you the exact request for your embryos' PGT-A file — written for your lab.
Step 02
Read against both partners' genomes, your embryos' existing PGT-A data shows which pregnancy-loss genes each one inherited, then places each on a risk curve per condition.
Step 03
A genetic counselor goes through every embryo with you — what each score means, and what it doesn't.
Sample report
The same report Core gives you, plus a score for every condition on the list.
Illustrative example. Your findings and recommendations will depend on your results and clinical history.
Embryo Report · Complete
24 findings per embryo
1 pregnancy-loss screen + 23 scored conditions
One result per embryo: its chromosome result, plus any pregnancy-loss gene fault it inherited from the 750+ genes screened in both of you.
Scores estimate genetic predisposition against a reference population. Non-genetic factors shape health too.
How each embryo is ranked, and how a modeled risk estimate differs from a diagnosis. Read the full method.
Complete includes everything in Core — each embryo's chromosome result, a pregnancy-loss and fertility gene review, and the full 750+ gene panel for both partners — and adds modeled risk estimates for 24+ health conditions and traits on every embryo. Genetic counseling and downloadable data are included.
Core focuses on pregnancy-loss and fertility findings for $750. Complete is $1,000 and includes everything in Core, then adds 24+ health conditions and traits for every embryo.
No new biopsy or test is needed — we use the PGT-A data from your already-tested embryos. Compatibility depends on how your embryos were sequenced, so we review your files and confirm before you pay anything for embryo analysis.
Our models are trained on individual-level genomes from large biobanks, not the GWAS summary statistics behind most polygenic scores. We then test the question your report actually asks: does the score separate sibling embryos, not just unrelated people? Complete is $1,000 for all embryos, all cycles; comparable reports elsewhere run $10,000 or more.
No. A score estimates genetic predisposition relative to a reference population. It is not a diagnosis and not a prediction of whether a child will develop a condition. Diet, environment, chance, and factors no genetic model captures all matter, and no embryo-ranking scheme is validated by prospective outcome data yet.
Most published polygenic research is on people of European ancestry, so that is where scores have historically been strongest. We train and validate across several biobanks — including NIH's All of Us, built specifically to redress that gap — using methods designed to carry across ancestries, and this is improving quickly. Your counselor will tell you what it means for your report.
Your report ranks every embryo by best fit for transfer — chromosome result first, then pregnancy-loss genes, then the health conditions weighted by the priorities you set — with a counselor note on each. The decision is yours, made together with your care team.
No. $1,000 is a flat fee covering every embryo you have, across every cycle, with no per-embryo pricing.
It means the review found no reportable finding under current methods and evidence standards. It does not rule out every genetic factor or guarantee that a transfer will succeed. An eligible order with no qualifying result in either partner can request a full refund under the No-Finding Promise.
A human next step
Text us a quick question, or book a free conversation with Christina, our licensed genetic counselor, about your embryo data, what the health conditions do and don't tell you, and whether Complete fits.
Embryo Report Core is $750 and covers chromosomes and pregnancy-loss genes — no scores, no trait predictions.
The Infertility & Pregnancy Loss Panel screens both partners from an at-home saliva sample — no IVF needed to start.