Most patients already bought a DNA test — but the raw file doesn't tell them what to eat, how to train, or what to flag before surgery. You interpret wellness, clinical, and surgical findings, release a branded report they understand, and bill a consult for that visit.
The patient report
Three layers · reviewed by their provider · branded to your clinic
Every finding: what it means, what to do, and optional note from their provider.
For your clinic
You run the consult, attest to open clinical & surgical flags, choose what to release, and put your logo on the PDF — a billable visit that turns their old DNA file into care they trust.
6+
DNA formats patients already have
Branded
Report with your clinic identity
You decide
What each patient sees
$349
Typical consult clinics charge
Patients bring exports from any major provider. Your team reviews tiered findings, flags surgical risk for the right cases, and releases a branded PDF — not a raw data file.
Accept 23andMe, AncestryDNA, MyHeritage, FTDNA, Living DNA, tellmeGen, Genes for Good, and clinical VCF. One parse pipeline — patients use whatever they already have.
Your clinic logo, contact details, and ordering doctor on every disclosure PDF. Add a provider note; findings grouped with clear labels and required warnings.
Thrombophilia, anesthesia pharmacogenomics, iron overload, anticoag sensitivity, and more — surfaced for your team before elective surgery, never auto-sent to the patient.
Wellness insights and clinical findings stay separate. Clinical rows unlock only after counselor sign-off and a per-session professional attestation — then you release, retain, or refer.
Consent-gated ingest, envelope-encrypted raw DNA, tenant row-level security, and crypto-shred deletion. PII stays separated from genetic results.
Every medical-section open and every disclosure decision is hash-chained and immutable — your artifact when a patient asks what was shared and when.
Create your clinic account. Professionals act under it — no per-seat friction to start.
Capture informed consent. PII is encrypted and separated from the genetic layer by an opaque token.
Drop a file from 23andMe, AncestryDNA, MyHeritage, FTDNA, or VCF. Parsed and matched server-side; raw bytes stored encrypted.
Read tiered findings, attest to open clinical/surgical flags, then release a branded PDF — every action logged.
Patients don't want a spreadsheet of SNPs. They want a clear, professional-reviewed report with your clinic's name on it — something worth paying for and keeping.
Your logo, provider name, and contact info on a polished report — released only when you approve each finding.
Nutrition, caffeine, folate, fitness, and sleep — plain language matched to their DNA, not a generic template.
Add context in your own words. It appears on the PDF alongside curated marker copy and required disclaimers.
Consent up front, encrypted storage, and nothing shared without your explicit release decision.
Most clinics bill $299–$499 per genomic consult. Platform cost runs $59 pay-as-you-go or less on a Practice plan — strong gross margin on every patient you run.
Highly sensitive data deserves more than a checkbox. BonaGenesis engineered so that even an application bug can't cross a tenant boundary, and every clinical action leaves an immutable record.
Tenant scoping enforced in Postgres, below the app.
Per-record data keys; crypto-shred to delete.
rsIDs, genotypes, and patient refs never leak.
No analysis without a recorded consent.
Disclosure & access logs detect any tampering.
Counselors touch the library, never patient data.
Honest limit: this is defensible design, not legal clearance. BonaGenes is not a medical device and does not provide a diagnosis. A regulatory/healthcare attorney and a genetic counselor must sign off before launch.
Start with zero commitment, or commit for a lower per-patient rate. No locked-in report bundles, no paying for volume you don't use.
Zero commitment — pay only when you run a patient.
$0 /mo
$59 per patient you run
No per-patient charge until you run a patient. Cancel anytime.
We'll pick the cheapest plan for your volume automatically. A branded genomic consult or pre-op review typically bills well above platform cost — high margin for your clinic.
Gross margin
94%
$6,564 kept on $6,980 billed each month
Illustrative. Excludes your staff time and patient acquisition. Plan figures are current list pricing.
No. It is decision-support for a licensed professional. It surfaces curated, genotype-based insights and never provides a diagnosis. All clinical action is the professional's.
From a curated marker library, not the code. Counselors verify markers before they render, and curated fields are never auto-rewritten.
Raw DNA and PII are encrypted at rest, tenants are isolated with database row-level security, sensitive data never appears in logs or URLs, and every clinical disclosure is logged in a tamper-evident chain.
23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA, tellmeGen, Genes for Good text exports, and clinical VCF. Patients use whatever they already downloaded — your staff uploads it securely.
Yes. Upload your logo and contact details in Settings. Every disclosure PDF carries your branding, the ordering provider, optional provider notes, and a discrete BonaGenes footer.
Yes. Verified perioperative markers — thrombophilia, succinylcholine sensitivity, iron overload, warfarin metabolism, and related flags — appear in a dedicated surgical section for professionals. They are never auto-released to patients.
Not today. Access is clinic-mediated: you review findings and release a branded PDF when appropriate.
Request early access and we'll set up your clinic and a guided walkthrough. Already convinced? Create your account.