Innovative genetic and genomic research laboratory

Our goal is to transform complex genetic data into understandable, practical insights that help reveal disease risks early, accurately diagnose conditions, and personalize treatment.

Science-driven mission

At Genotipas, we believe that genetics only holds true value when it leads to clear decisions. That’s why our work is guided by three core principles: Knowledge, Action, and Well-being—a consistent path from accurate answers to meaningful health benefits for the patient.

Knowledge

Through advanced research, we provide clear answers about genetically determined risks.

Action

By turning this knowledge into practical advice, we help prevent diseases or choose the most effective treatment.

Well-being

We aim to make genetics a commonplace, accessible and easy to understand part of healthcare.

Why trust “Genotipas”?

We build trust not on promises, but on verified quality standards, international oversight, and transparent results.

Founded in 2017

8 years of specialization in medical genetics

ISO 15189

Operations follow international medical laboratory standards

Licensed specialists

Every test is supported by a qualified professional team

National healthcare license

Regulated under national healthcare system requirements

Network of licensed professionals and partners

A genetic test is only as valuable as its interpretation. That’s why our foundation is a multidisciplinary team of experts who ensure that your results are not only accurate, but actionable. Our team includes:

Certified laboratory medicine specialists

Experienced clinical geneticists

Dietitians who apply wellness principles

Gynecologists focused on women’s health

“Pharmacogenetic testing helps objectify medication selection strategies—especially in psychiatry, where many diagnoses are based on clinical symptoms rather than instrumental methods.”
Prof. D. Serapinas
“With the WID-easy test, taken from a simple vaginal swab, around 90% of women could avoid unpleasant invasive diagnostic procedures—without increasing the risk of missing cancer.”
Prof. Žana Bumbulienė

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