Medication research

DNA and pharmacogenetics

How the genetic code responds to medications, with the CYP and UGT genes that matter most and the reference study behind every result.

Results in 3–4 weeks

ADNTRO saliva kit box
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Look inside the reports

We'll give you access to an example account with the results of a real sample: ancestry, nutrition, fitness and research, exactly as you'll see your own.

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We process your data to give you access to the demo and to tell you what's new. You can unsubscribe whenever you want.

This is not a medical device

Results are calculated solely from public sources: PharmCAT, the open tool that translates the genotype into diplotypes, and the guidelines of the CPIC (Clinical Pharmacogenetics Implementation Consortium). They include no dosage or treatment recommendations and are for informational and educational purposes. They are not a medical diagnosis and do not replace a consultation with a healthcare professional: they are a tool to explore the genetic code, with the level of evidence and the limits of every result in plain sight.

ADNTRO saliva kit box
Saliva kit

The most comprehensive genetic test

€169 €199 −15%

  • Full ancestry report
  • More than 300 results
  • Personalized nutrition recommendations
  • Fitness and longevity profile
  • Research tools for your own genetic variants
  • Personality traits with a genetic basis
  • Longevity and aging indicators
Buy your kit

Secure payment by card or PayPal · Results in 3–4 weeks

Information based on simple search.

Have you already taken a DNA test? Upload your file and skip the kit

Who we work with and what backs us

What the report includes

How the genetic code responds to medications

More than 60 reports in pharmacogenetics, each with its gene and reference study: the gene families that matter most in how your body processes a medication, from CYPs to UGTs.

More than 60 reports

How the metabolizer profile fits with the most common treatments, from painkillers to metabolic medications.

The metabolizer profile

How fast each family of medications is processed. What matters most are the CYP genes —CYP2D6 and CYP2E1 among them— and the UGT and SULT conjugation enzymes.

Risk of adverse effects

Which treatments your genetics associates with a higher chance of side effects, and which with lower effectiveness.

The PDF report

Downloadable results, each citing the study it comes from.

Results are for research and education: they are not a medical diagnosis and do not replace a consultation with a healthcare professional. No medication plan is decided from this information, which includes no dosage or treatment recommendations.

Who vouches for the science

Behind every report are named people

Dr. Jair Tenorio-Castaño

Geneticist

Geneticist and researcher at the Instituto de Genética Médica y Molecular of Hospital Universitario La Paz. Co-authors our polygenic risk score publications, and his ORCID lists the rest of his work.

Co-authorship on 2 of our publications

Qualifications and affiliations

  • ADNTRO Genetics
  • INGEMM · Hospital Universitario La Paz / IdiPAZ
  • CIBERER · Instituto de Salud Carlos III
  • ERN-ITHACA · European Reference Network
View ORCID

What your results look like

Your variants, gene by gene

Which version of each metabolism gene you carry, with its public identifier and its genotype. The data as it is, to research it and to take it to whoever treats you.

ADNTRO platform Medication research · Metabolism Example M

Phase I metabolism

Gene Variant rsID Genotype Interpretation
CYP1A1 *2C Ile462Val rs1048943 TT Ile/Ile: the reference form of the gene.
CYP1A1 *2A MspI rs4646903 AA Together with rs1048943, CYP1A1 with no variants (wt/wt).
CYP1A2 *1F rs762551 AC *1A/*1F: intermediate inducibility of the enzyme.
CYP1B1 *3 Leu432Val rs1056836 CG Leu/Val (wt/*3): one copy with higher activity towards 4-hydroxylation.

Genetics has an influence, but on its own it doesn't determine your health or your performance. These results are informational and do not constitute a medical diagnosis.

The data is fictitious.

How does ADNTRO's DNA test work?

Get your kit

Buy your kit and receive it at home.

Take your sample

Saliva, at home, in two minutes. No needles, and no personal data required.

Get your results

In 3–4 weeks you'll have all your results in your private account.

Woman with a cup by her living room window, with the ADNTRO saliva kit on the side table
GeneAI

Talk to your DNA

GeneAI reads your results and explains them in plain language. Ask it anything, as many times as you need, until you get it.

Things people ask it

  • What does my DNA say about my sleep?
  • Should I train for strength or endurance?
  • Which genetic variants influence vitamin D?
  • Where does my Italian ancestry come from?
Discover your DNA

Included with the Premium kit and the subscription.

Example conversation

  1. You

    Why doesn't afternoon coffee agree with me?

  2. GeneAI

    You have the slow version of the gene that metabolizes caffeine, so it can still be affecting you several hours after you drink it. Genetics explains part of it; sleep habits and routine explain another part that matters just as much.

    CYP1A2 rs762551 A/C High evidence
  3. You

    Explain it to me like I know nothing about genetics.

  4. GeneAI

    Your body takes longer than normal to switch off caffeine's effect. If you have it in the mid-afternoon, it's likely still working by the time you go to sleep.

GeneAI explains your results. It is not a medical diagnosis and does not replace consultation with a healthcare professional.

Buy it

Discover the secrets of your DNA for €169

This report is included only in the Premium kit.

Secure payment by card or PayPal · Results in 3–4 weeks

Have you already taken a DNA test? Upload your file and skip the kit

Seven areas, one sample

What does ADNTRO's genetic test offer?

ADNTRO's DNA test offers you more than 300 reports across six categories: ancestry, nutrition, fitness, longevity, personality and fertility.

Ancestry

Which populations you come from and in what proportion, with your maternal and paternal haplogroups.

Nutrition

How you process lactose, gluten, caffeine, or fat, and which vitamins are harder for you to absorb.

Fitness

Whether your profile leans more toward strength or endurance, your recovery, and your injury risk.

Longevity

The genetic traits associated with aging and the passing of time.

Health research

Genetic results backed by more than 300 GWAS studies, each with a direct link to the original publication.

Personality

Behavioral traits with a described genetic basis: sleep, sensitivity, appetite.

Fertility

Hormonal balance through your genes.

Maximum privacy and security

Your data is anonymous, and only you have access to it

We don't offer relative matching, in keeping with our principle of total sample anonymity.

Read the privacy policy
  • We don't sell or share your data

    We will never share or sell your data. When the chance to contribute to a scientific study comes up, we ask for your voluntary consent, and you can say no.

  • European servers

    Your data is processed on European Google Cloud infrastructure, under GDPR.

  • Your data is always yours

    You can download your data and delete all our records at any time, no explanation needed.

Scientific standard

Are DNA tests reliable?

Yes, when they use validated technology. ADNTRO analyses ~700,000 markers with an Illumina GSA chip in an ISO 15189-certified laboratory (Eurofins, Denmark), and its risk models are published in peer-reviewed journals.

  • Variants with evidence described in peer-reviewed literature
  • Purpose: education, information and research on your own DNA (never a diagnosis)
  • Genotyping in a certified European laboratory
  • Results linked to the study they're based on, its population and sample size
  • UK Biobank as our validation base
See our publications
Cover of the article "Type 1 diabetes risk with neural networks", published in Int. J. Mol. Sci. in 2026Cover of the article "Late-onset Alzheimer's and polygenic risk score", published in Genes in 2025
Peer-reviewed, open access articles: you can open them and check the method yourself.

What our customers say

Jessica H.

I love it. Very informative.

@roman_nfkrz Let's get into my DNA test, see what it's all about and learn some science!
MissR

Love the insights they provide to my health journey. Brilliant data points to better understand how to improve your healthcare. They always come up with new markers.

Debbie

Our results show info missing on other tests but validated by years of family tree research. Really helped pull it all more together.

@francescapsychology Understanding your background can help you understand yourself.
Tonio A.

I like the reports, very detailed.

@jaydonehistory Ready to discover what your DNA says about you?
April

My experience with them was great. An informative and upstanding company.

Have data from AncestryDNA, MyHeritage or a Whole Genome? Upload it to ADNTRO

If you already have a raw file from AncestryDNA, MyHeritage, 23andMe or another provider, you can upload it to ADNTRO and access more than 300 reports on wellness, ancestry, nutrition, personality, longevity, fitness and fertility without a new test. We also accept the VCF file of a whole genome (WGS), not just genotyping files.

  • 23andMe
  • MyHeritage
  • AncestryDNA
  • FamilyTreeDNA
  • Tellmegen
  • Others

Frequently asked questions

Is this a medical diagnosis?
No. Results are for research and educational purposes, and they don't replace consultation with a healthcare professional. We calculate your predisposition from published genetic association studies (GWAS), so you can explore your genetic code with context.
What do I need to take the test?
Just your saliva. The kit arrives at your door with everything you need and the instructions. No needles, and no fasting required.
How long until I get my results?
Between 3 and 4 weeks from when we receive your sample. We email you at every step.
Who can see my data?
Only you. We don't ask for personal data when you register the kit, so not even we can link a sample to a person.
Do I have to pay for a subscription?
Not to access your reports. The subscription gives you access to updates and features like GeneAI; the first three months are free, and after that it costs €25 a year.

Your genetics are part of your story

Start there.

Discover your DNA
Discover your DNA