DNA Test Interpretation
A comprehensive genetic health report: findings by health area, pharmacogenomics, nutrigenomics, disease risks, carrier status, traits, follow-up tests and red flags.
Supported DNA filesNew · 23 September 2026
AI DNA test interpretation for clinics
Upload raw DNA data or a genetic report and get a comprehensive genetic health report in minutes: pharmacogenomics, nutrient metabolism, disease risks and carrier status, checked against the patient's own file and written in 100+ languages.
- 334 curated DNA markers
- 20 health areas
- 100+ report languages
- Print-ready PDF with your logo
What is AI DNA test interpretation?
A consumer DNA test such as 23andMe, AncestryDNA or MyHeritage reads hundreds of thousands of genetic markers. The raw file holds the answers to many clinical questions, but in a form nobody can read: long lists of rsIDs and letter pairs. AI DNA test interpretation turns that file into findings a clinician can act on.
Kantesti compares the file with a curated panel of 334 markers in 20 health areas, from methylation and cardiovascular genes to drug response, nutrient metabolism and carrier status. An AI model writes the report; every finding is then checked against the file itself, so the report cannot invent a result the patient does not carry.
Three AI modules, one genetic picture
Start with the DNA report, then combine it with the patient's blood test and questionnaire.
DNA + Blood Health Report
Genes meet lab values. See where a genetic finding and a blood result confirm or contradict each other, with a risk matrix, priority actions and a monitoring plan.
How DNA + Blood worksSupplement Advisor
A personalised supplement plan from DNA, blood test and a short questionnaire, with doses, timing, interactions and re-test dates, built on your clinic's own products.
About the supplement planHow it works
- 1
Load the patient
Open DNA Health in the Kantesti clinic panel, choose the patient and the report language.
- 2
Upload the DNA data
A raw DNA file (also zipped), pasted rsID lines, or a genetic report as up to 6 PDF, JPG or PNG files.
- 3
Review the report
The genetic health report is ready in a few minutes, with every finding tied to the genotype in the file.
- 4
Combine and print
Add the patient's blood test and questionnaire, then print or save each report as an A4 PDF with your clinic's logo.
AI DNA test interpretation, illustrated
Works with the DNA tests your patients already have
Raw data files from the major consumer DNA services and VCF files are read directly. A genetic report from any laboratory can be uploaded as PDF or photos.
- 23andMe
- AncestryDNA
- MyHeritage
- FamilyTreeDNA (FTDNA)
- LivingDNA
- VCF
- PDF genetic report
- Photos of a printed report
- Pasted rsID lines
How the AI reads a DNA file
Five steps between the raw file and the clinical report, and the check that keeps the AI honest.
-
Raw DNA file
23andMe, AncestryDNA, MyHeritage, FTDNA, LivingDNA or VCF, also zipped.
-
334-marker panel
The file is parsed on the server and matched to the curated panel.
-
AI interpretation
The model writes findings for 20 health areas, drug response and nutrition.
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Checked against the file
rsIDs not in the file are removed; genotypes are pinned to the file's calls.
-
Clinical report
In 100+ languages, print-ready with your clinic's logo.
What the report covers
334 curated markers, grouped into 20 health areas.
- 01
Methylation & B vitamins
MTHFR, MTR, MTRR and the folate cycle
- 02
Cardiovascular
Blood pressure, heart rhythm and vessel health
- 03
Lipids & cholesterol
APOE, LDL, triglyceride and Lp(a) variants
- 04
Metabolic & diabetes
Insulin response and type 2 diabetes risk
- 05
Weight & appetite
FTO, MC4R and appetite regulation
- 06
Vitamins & minerals
Vitamin D, B12, iron and other nutrients
- 07
Food response
Lactose, gluten, caffeine and alcohol response
- 08
Detoxification
Oxidative stress and detox enzymes
- 09
Inflammation & immunity
Inflammatory and immune markers
- 10
Autoimmune
HLA tag markers
- 11
Pharmacogenomics
34 drug-response markers, CYP2C19, CYP2D6, SLCO1B1 and more
- 12
Blood, iron & clotting
Factor V Leiden, prothrombin, HFE
- 13
Bone & joint
Bone density and joint markers
- 14
Hormones
Hormone metabolism markers
- 15
Brain, mood & sleep
COMT, circadian and neurotransmitter genes
- 16
Fitness & recovery
Muscle type, endurance and recovery
- 17
Longevity & ageing
Markers linked with healthy ageing
- 18
Cancer predisposition
Tag markers, always to be confirmed clinically
- 19
Carrier status
Tag markers for recessive conditions
- 20
Traits
Non-medical traits
Checked against the patient's own file
Generic AI tools can write a convincing genetic report about variants the patient does not have. Kantesti cannot: the raw file is parsed on our server first, and the report is then validated against it.
- An rsID that is not in the file is removed from the report.
- Each genotype is pinned to the call printed in the file.
- The data-quality section shows the file format, genome build, call rate and how many panel markers were found.
- Carrier and cancer tag findings are always marked for confirmation by clinical genetic testing.
334curated DNA markers
20health areas
100+report languages
39interface languages
Methodology and sources
How the panel and the reports are built, and the public references behind them.
Curated marker panel
334 markers identified by their dbSNP rsIDs, each assigned to one of 20 health areas with its gene and trait.
dbSNP, NCBIPharmacogenomics
Predicted metabolizer phenotypes use the terminology of the Clinical Pharmacogenetics Implementation Consortium (CPIC). The report names affected drug classes and never gives prescription doses.
CPICSupplement limits
Doses stay within the tolerable upper intake levels published by health authorities.
EFSA dietary reference valuesEvidence levels
Every finding is graded established, probable or preliminary, so the clinician can weigh it.
Validation against the file
Findings written by the AI are checked against the uploaded file before the report is shown.
Made for clinics
DNA Health is part of the Kantesti clinic panel, next to blood test interpretation, trends, nutrition and family health.
Your brand on every report
Print-quality A4 PDF with your clinic's logo, address and contact details on every device.
100+ report languages
Write the report in the patient's language. The interface is available in 39 languages.
One patient record
DNA reports sit with the patient's blood tests, so combining them takes one click.
API for integrations
The same three modules as a REST API, with sandbox and async mode.
API documentationFrequently asked questions
Which DNA tests can be interpreted?
Raw data files from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA and LivingDNA, VCF files, pasted rsID lines, and genetic reports from any laboratory as PDF or photos.
How long does a DNA report take?
Usually one to three minutes. The raw file is read in seconds; the rest is the AI writing and validating the report.
Is the report a diagnosis?
No. It is clinical decision support for the treating clinician. Consumer genotyping is not clinical sequencing, so actionable and carrier findings should be confirmed with validated clinical genetic testing.
Can the DNA report be combined with a blood test?
Yes. The DNA + Blood Health Report combines it with one of the patient's interpreted blood tests, and the Supplement Advisor uses both together with a short questionnaire.