Reveal the underlying causes of complex symptoms with advanced genetic diagnostics.
Clinical Genetics
In-depth analysis of your genome to reveal important clinical information
DKK 16.500,-
Book nowIncl. doctor consultation
A comprehensive investigation into the genetic foundations of your health.
Our Clinical Genetics analysis uses advanced whole-exome testing to help uncover whether unexplained symptoms or conditions - such as metabolic, neurological, or inherited diseases - may have an underlying genetic cause.
The exome represents just 2% of the genome, yet holds around 85% of all known disease-causing variants.
This analysis aims to pinpoint potential symptom triggers, minimise uncertainty, and enable informed dietary and lifestyle decisions.
The key areas we decode
All protein-coding regions (exons)
The parts of your DNA that provide the instructions for building your body's proteins - where most disease-causing variants are found.
Clinically relevant intronic and intergenic positions
Important areas between genes that can still influence how genes function and may play a role in certain conditions.
Mitochondrial genome variants
Changes in the DNA found in your cells' energy-producing structures, which can affect metabolism and inherited conditions.
Genome-wide copy number variants (CNVs)
Larger genetic changes - such as missing or extra sections of DNA - that can impact development, disease risk, and how the body functions.
The value of understanding your genetic blueprint
Genetic conditions are often subtle - until they are not
Many hereditary variants cause symptoms that appear gradually or mimic common complaints such as fatigue, pain, or developmental differences.
Symptoms may span multiple systems
Genetic conditions can influence metabolism, neurology, immunity, connective tissue, hormones, cardiovascular function, and developmental pathways.
Clarity brings direction
A confirmed genetic explanation helps guide more precise treatment, referrals, and lifestyle planning - and reduces unnecessary worry or testing.
Curiosity or concern about hereditary risks
Understanding your genetic architecture provides clarity for your own health - and your family's. Inherited disorders often present in recognisable but complex patterns.
How does it work?
Our clinical genetics workflow designed to identify the genetic causes of complex symptoms with the highest level of precision.
Clinical Genetics
DKK 16.500,-
In-depth analysis of your genome to reveal important clinical information
What's included:
Important information:
You'll provide a blood sample during your visit. The process is simple, fast, and supported by experienced clinical staff.
After the blood sample is taken, you will meet with the doctor, who will review potential symptoms, relevant diagnoses, family history, and other important health factors.
After 5-6 weeks you're results are ready. A genetic counsellor will review your results before you discuss them with your clinical doctor. In the doctor consultation you will be able to ask questions, understand your findings, and receive personalised recommendations.
Your report highlights identified variants, risk markers, CNVs, and inheritance patterns - supported by clear medical interpretation and practical guidance for next steps.
Ready to understand your genetics?
Get meaningful, clinically guided insight into your hereditary risks and the genetic factors that may influence your health.
Clinical Genetics
In-depth analysis of your genome to reveal important clinical information
DKK 16.500,-
Book nowLearn more about Clinical Genetics
You will receive clear guidance on how to prepare for your visit. No fasting is required.
We will ask you to create a family pedigree that includes your relatives' diagnoses, diseases, and symptoms. If you have a medical condition yourself, we will also ask you to prepare a medical timeline of your illness and any medications you have taken or are currently taking.
Please plan for a total visit time of around 30 minutes. This includes a blood draw and a consultation with the physician.
If we identify a pathogenic or likely-pathogenic variant, or a significant CNV, we discuss next steps immediately. This may include follow-up testing, family screening, referrals, or targeted treatment considerations.
Join our newsletter for research highlights and practical guidance.