Evartia Metabolic Home Test Kit (Evartia)
Results ready within 3-4 weeks
UKAS accredited laboratory, ISO 15189.
How it works
Your testing journey
From order to results in four simple steps. Full transparency on where each step happens and what it costs.
Receive your kit by post
Dispatched same working day if ordered before 3pm. Royal Mail Tracked delivery, typically 1–3 working days. 90% of kits arrive within 24 hours.
Collect at home
Everything you need is in the kit. Collect your sample in the privacy of your own home — no appointment needed, no clinic visit.
Included in kit price
Saliva sample at home
Spit into the collection tube until the liquid reaches the indicated line. Seal and post back. About 5 minutes of gentle spitting.
Return by prepaid envelope
Seal your sample in the biohazard bag provided and drop it in any Royal Mail postbox using the prepaid Tracked 24 envelope. Post Monday–Thursday for best results.
Find out if you have an inherited metabolic disorder that could be affecting your health. Evartia is a comprehensive genetic test that detects mutations in 223 genes involved in metabolic pathways—helping you understand, manage, and treat metabolic conditions before they cause serious complications.
Metabolic pathways play essential roles in keeping our bodies healthy, including producing energy and extracting nutrients from the foods we eat. When a genetic mutation occurs in a metabolic pathway, it can lead to a buildup of toxic substances or insufficient production of essential products, affecting health and development.
The test uses a simple, painless cheek swab—no needles, no blood. Whether symptoms appeared at birth, in childhood, or are only now emerging in adulthood, Evartia can help identify the underlying cause and guide your treatment.
Why Choose Evartia?
- Comprehensive 223-gene panel – Covers all major categories of inherited metabolic diseases
- Simple cheek swab – Painless collection, no needles, no blood
- Understand your condition – Know what you have and how it may progress
- Guide treatment decisions – Help your doctor choose the best clinical management
- Identify at-risk family members – Know who else should be tested
- Results in 2–3 weeks – From sample arrival at the laboratory
What Can Evartia Help You Identify?
- Diseases you may currently have
- Your prognosis—how the disease will progress based on your specific mutation
- The best treatment and clinical management for you
- Complications you should be aware of
- How it will affect your life
- Who in your family should be tested
- Who can help you—specialised doctors, dieticians, support groups
Symptoms of Metabolic Diseases
Symptoms of inherited metabolic diseases usually appear shortly after birth. However, depending on the mutation, the metabolic pathway involved, and the severity of the condition, some people develop symptoms in early or late adulthood.
Symptoms can also occur suddenly due to:
- Specific foods or medications
- Dehydration
- Illness or infections
- Physical stress or other triggers
With Evartia, detecting and managing a metabolic disorder early can prevent or reduce symptoms, avoid chronic health consequences, and improve your quality of life.
Results are available within 2–3 weeks from the sample arriving at the laboratory. Please allow up to 4 weeks to receive your results from the date of purchase.
How It Works
We'll send you a collection kit with buccal swabs (cheek swabs), simple instructions, and a prepaid return envelope. Just swab the inside of your cheek—it's completely painless and takes less than a minute. No needles, no blood, no clinic visit needed.
Your kit includes: Buccal swab collection materials, step-by-step instructions, consent form, and prepaid return envelope.
Who Is This For?
- Anyone with unexplained symptoms that could indicate a metabolic disorder
- People with a family history of inherited metabolic diseases
- Individuals experiencing symptoms triggered by certain foods, medications, or illness
- Parents of children showing developmental delays or unexplained health issues
- Adults with late-onset symptoms seeking a diagnosis
- Anyone wanting to understand their metabolic health at a genetic level
Evartia covers all major categories of inherited metabolic diseases through a comprehensive panel of 223 genes involved in metabolic pathways.
Amino Acid Disorders
Organic Acid Disorders
Fatty Acid Oxidation Disorders
Carbohydrate Disorders
Lysosomal Storage Disorders
Other Metabolic Conditions
Good to Know
Evartia is a genetic screening test that identifies mutations linked to inherited metabolic diseases. A positive result indicates you carry genetic variants that may be causing or contributing to metabolic dysfunction.
Many metabolic conditions can be managed effectively with dietary changes, supplements, medications, or other interventions—especially when detected early. Your results can also help identify other family members who may benefit from testing.
We recommend discussing your results with a metabolic specialist, genetic counsellor, or your GP. They can help you understand what your results mean and connect you with the right healthcare professionals, dieticians, and support groups.
Sample Collection: Saliva sample collected at home.
No Fasting Required.
Results Timing: 3-4 weeks.
You may also be interested in
Genetic Health Test
A comprehensive at-home DNA health test analysing 187+ genetic markers across more than 20 health and wellness categories — covering nutrition, fitness, metabolism, hormones, and disease predisposition, processed by Eurofins laboratory.
Results estimated in 3-4 weeks
Finger-prick collection
Complete Genetic & Biological Age Test
A comprehensive at-home DNA test combining 187+ genetic health markers with epigenetic profiling for biological age and methylation analysis — all from a single saliva sample, processed by Eurofins laboratory.
Results estimated in 3-4 weeks
Finger-prick collection
Epigenetic Age Test (biological age)
An at-home epigenetic test measuring your biological age at the cellular level through DNA methylation patterns — revealing how your body is ageing compared to your chronological age, analysed by Eurofins laboratory.
Results estimated in 3-4 weeks
Finger-prick collection
Cardiovascular Test (Ventrilia)
A next-generation genetic test (Ventrilia) screening for inherited mutations linked to hereditary cardiovascular syndromes including familial hypercholesterolaemia, cardiomyopathies, and arrhythmia risk — ideal for people with a family history of early cardiovascular disease.
Results estimated in 3-4 weeks
Finger-prick collectionNo clinics, no queues, no hassle
Four steps to clarity
Pick your panel
Browse over 200 clinically designed test kits and choose the one that fits your goals.
Kit to your door
Everything you need arrives in discreet packaging with step-by-step instructions inside.
Collect your sample
Follow the simple instructions in your kit - whether it is a finger-prick at home or a venous draw at a partner clinic, your test page will guide you.
Insights delivered
Clear, easy-to-understand results sent to you online with actionable health guidance.