Submit existing genetic data
Upload raw genetic data or a genetic/nutrigenetic report. We assess supported files and platforms before analysis.
Specialist nutrigenetic interpretation
Turn existing DNA data into actionable nutrition insights.
Your client already has the DNA. We help you understand what matters — in context, with evidence, and around the goals that matter to them.
✓No new DNA test required. We work with data your client already has.
Interpretation pathway / 001Evidence-led
01 / Input
Raw genetic data
rs1801133 AGrs9939609 ATrs1801280 CCrs7903146 CT+ 684 available variants
File assessed
↘
02 / Context
Biological interpretation
Client goal→Pathways→Evidence
Variants are reviewed alongside phenotype, symptoms, lifestyle and current evidence.
Phenotype-informed
↘
03 / Output
Practitioner priorities
P1Glucose regulationHigh
P2Lipid responseModerate
—Inflammatory signallingMonitor
Decision support
01Goal-oriented
02Pathway-based
03Evidence-graded
04Practitioner-led
The gap
Your clients already have the data. What they often don’t have is a useful interpretation.
More clients are arriving with raw DNA files, old nutrigenetic reports and consumer test results. What they need from you is not another long list of SNPs — it is clarity about which findings are relevant to their goals, phenotype and next conversation.
You should not have to spend hours researching individual variants, reconciling conflicting recommendations or deciding what deserves clinical attention.
That’s where we come in.Specialist interpretation, ready for your consultation.
01Raw DNA filesConsumer genotyping data in unfamiliar formats.
02Old reportsPages of findings without prioritisation.
03Conflicting adviceRecommendations that don’t agree with the phenotype.
04Too many variantsHundreds of signals, few clear decisions.
Our difference
We don’t just interpret SNPs.
We interpret them around your client’s goals.
Each case begins with the question you are trying to answer — then moves through phenotype, pathways and evidence to identify what deserves priority. No isolated-variant theatre. No generic automated report.
01Client goalWhat are we trying to understand?
02PhenotypeWhat is present in real life?
03Biological pathwaysWhich systems are relevant?
04Genes & variantsWhat data is available?
05Scientific evidenceHow strong is the signal?
06ConcordanceDo genotype and phenotype align?
07PrioritiesWhat should guide the next step?
Start with a focusUp to three primary goals per case.
Weight & metabolism
Gut health & bloating
Energy & mitochondrial function
Sports performance & recovery
Nutrient metabolism
Healthy aging
The process
From existing file to a clearer practitioner conversation.
Five structured steps keep the work focused, transparent and useful in practice.
Define the client’s priorities
Select up to three goals and share relevant phenotype, clinical and lifestyle information through a structured questionnaire.
Pathway-based analysis
Relevant phenotypes, biological pathways, genes and available variants are identified for the selected objectives.
Review & evidence grading
Findings are reviewed for biological relevance, scientific support and genotype–phenotype concordance.
Receive your practitioner report
A structured report designed to support professional nutritional decision-making and your client conversation.
The output
Not another automated DNA report.
The value is not in making the list longer. It is in making the next decision clearer.
Typical genetic report×
- Long list of SNPs
- Risk alleles without context
- Generic recommendations
- Little prioritisation
- Limited phenotype integration
Our practitioner interpretation✓
- Goal-oriented
- Pathway-based
- Phenotype-informed
- Evidence-graded
- Prioritised and professionally reviewed
Which findings matter most for this client?Do genotype and phenotype point in the same direction?Which findings should not drive an intervention?
Illustrative example
Example — Nutrigenetic Priority Map
Simulated data only. A view of how a practitioner report turns many signals into a focused conversation.
Case focus / metabolism + energy
P1 High priorityP2 SecondaryMonitor
AreaGenetic signalPhenotypeEvidencePriority
Glucose regulationHighPresentStrongP1
Satiety & appetiteHighPresentModerateP1
Lipid responseModerateAbsentStrongP2
Mitochondrial efficiencyModeratePresentModerateP2
Inflammatory signallingLowPresentEmergingFurther assessment
Priority is a function of signal, phenotype and evidence — not genetics alone.ILLUSTRATIVE / NOT A REAL PATIENT
Context matters
Genetics does not exist in isolation.
Genetic information is interpreted in context, rather than automatically converted into dietary recommendations.
Phenotype
Genetic signal
Present
Absent
Present
High interpretation prioritySignal and phenotype point in the same direction.
Contextualise / monitorSignal is present, but the phenotype is not.
Absent
Look beyond geneticsPhenotype deserves attention from other inputs.
Low priorityNo strong signal and no phenotype present.
Evidence system
Not every SNP deserves
the same weight.
Transparency includes showing where the science is strong, where it is limited, and when an interesting finding should not drive intervention decisions.
LEVEL ASTRONG
Replicated evidence, strong human data, meta-analyses or well-established associations.
LEVEL BMODERATE
Several supportive human studies, with meaningful limitations that remain.
LEVEL CEMERGING
Biologically plausible but preliminary, inconsistent or insufficiently replicated.
—NOT ACTIONABLE
Scientifically interesting, perhaps, but not suitable to drive an intervention.
Sometimes the most valuable interpretation is knowing which genetic findings not to overinterpret.
What you receive
Your practitioner report.
Built for a professional consultation — not for a consumer to interpret alone.
Request a sample report ↗DPractitioner
Interpretation
Interpretation
01—15
Report contents10–15 pages*
- Executive priority map
- Phenotype profile
- Relevant biological pathways
- Key genes & available variants
- Genetic interpretation + concordance
- Evidence grading + priority areas
- Nutrition-related considerations
- Biomarkers, limitations & methodology
Your practice, your judgement
You keep the client relationship.
We provide the genetic interpretation.
The service does not replace professional judgement. You remain responsible for the client consultation, diagnosis where applicable, nutritional strategy and follow-up.
NYou remain the practitioner.
We become your nutrigenetic interpretation partner.
We become your nutrigenetic interpretation partner.
Practitioner pricing
Start with one case.
Build from there.
Expert, phenotype-informed nutrigenetic interpretation for your clients.
FIRST PRACTITIONER CASEPilot
€199
Introductory pilot price for a practitioner’s first DNAReframe case.
- Review of existing genetic data or nutrigenetic report
- Up to 3 client health or nutrition goals
- Structured phenotype assessment
- Goal-oriented genetic interpretation
- Biological pathway analysis
- Relevant gene and variant analysis
- Genotype–phenotype concordance
- Scientific evidence grading
- Prioritisation of relevant findings
- Practitioner-focused interpretation
- Professional DNAReframe Practitioner Report
- Methodology and limitations section
Pilot access — one first case per practitioner
Submit your first case ↗SINGLE PRACTITIONER CASERecommended
€299
Standard professional interpretation for subsequent individual cases.
- Review of existing genetic data or nutrigenetic report
- Up to 3 client health or nutrition goals
- Structured phenotype assessment
- Goal-oriented genetic interpretation
- Biological pathway analysis
- Relevant gene and variant analysis
- Genotype–phenotype concordance
- Scientific evidence grading
- Prioritisation of relevant findings
- Practitioner-focused interpretation
- Professional DNAReframe Practitioner Report
- Methodology and limitations section
Full DNAReframe professional analysis for an individual client.
Submit a case ↗5-CASE PRACTITIONER PACK
€1,350
€270 per case. For practitioners integrating DNAReframe regularly into their practice.
Each case includes the same full professional analysis provided in the Single Practitioner Case:
- Up to 3 client goals
- Phenotype-informed interpretation
- Pathway-based analysis
- Relevant gene and variant assessment
- Genotype–phenotype concordance
- Evidence grading
- Priority mapping
- Professional Practitioner Report
10-CASE PRACTITIONER PACK
€2,500
€250 per case. Designed for established practitioners and clinics managing recurring nutrigenetic cases.
Each case includes the same core professional DNAReframe analysis as the Single Practitioner Case:
- Up to 3 client goals
- Phenotype-informed interpretation
- Pathway-based genetic analysis
- Relevant gene and variant assessment
- Genotype–phenotype concordance
- Evidence grading
- Priority mapping
- Professional Practitioner Report
Need higher volumes?
Volume pricing, recurring practitioner partnerships and white-label solutions are available for clinics and professional practices requiring regular analysis.
Contact us ↗DNAReframe provides specialist nutrigenetic interpretation and decision-support information for qualified professionals. The practitioner remains responsible for the client relationship, professional judgement, nutritional strategy and follow-up.
Built for
Qualified professionals who want more clarity, not more complexity.
Registered dietitiansNutritionistsFunctional & integrative medicineLongevity practitionersSports nutrition & performancePersonalised nutrition clinics
✓ Encounter clients with existing genetic tests
✓ Want to integrate nutrigenetics into practice
✓ Need more than an automated SNP report
✓ Want evidence-informed interpretation connected to phenotype
Compatibility
Already have a client in mind?
You do not automatically need another genetic test. If your client already has genetic data, we may be able to work with what they have.
Upload a sample or submit information about the platform used and we will assess compatibility before beginning the analysis.
23andMeAncestryDNAMyHeritageNutrigenetic labsSNP arraysOther raw data formats
Check a DNA file ↗Professional positioning
Useful, careful, and clear about limits.
01
Genetic associations are not deterministic. Multifactorial traits depend on genetics, phenotype, lifestyle and environment.
02
No SNP should be interpreted in isolation. Findings are prioritised according to available evidence and context.
03
This is decision support and specialist interpretation — not standalone medical diagnosis or clinical genetic counselling.
Questions
Frequently asked questions.
Can I submit a 23andMe or AncestryDNA file?+
Potentially. We assess the specific file format and available data before beginning the analysis. Compatibility is not universal.
Do you require a new genetic test?+
No. The service is designed to begin with existing raw data or an existing genetic/nutrigenetic report whenever the available information is suitable.
What happens if the client only has a PDF report?+
Submit the report for an initial assessment. We can clarify what can and cannot be reinterpreted from a PDF before analysis begins.
How many health goals can I submit?+
Up to three primary goals per case, selected by the practitioner.
Can I use the report with my own clients?+
Yes. The report is designed as professional decision-support information for use within your own client relationship.
Do you prescribe the diet?+
No. We provide specialist interpretation and nutrition-related considerations. You remain responsible for the nutritional strategy and professional advice.
How long is the report?+
Approximately 10–15 pages depending on case complexity and the selected objectives.
What if the file does not contain the variants needed?+
We will explain what can be assessed, what cannot be concluded, and whether the available data is sufficient to proceed.
How do you grade scientific evidence?+
Findings are grouped into strong, moderate, emerging and not actionable based on human evidence, replication, biological relevance and genotype–phenotype concordance.
How are genetic data handled and protected?+
Secure handling of genetic data is a core part of the service. Detailed privacy, consent, processing and retention information will be provided before submission.
Can clinics request white-label reports?+
Volume pricing and white-label solutions will be available for clinics and professional practices. Contact us at dnareframe@outlook.com to discuss requirements.
Do you interpret disease-causing mutations or diagnostic medical genetics?+
No. The service focuses on nutrigenetic and complex-trait interpretation. It does not replace clinical genetic counselling, diagnostic medical genetics or medical diagnosis.
For health professionalsThe DNA already exists.
The DNA already exists.
Let’s make it useful.
Turn existing genetic data into a structured interpretation built around your client’s real goals.
DNAReframe | Practitioner Teamdnareframe@outlook.com