A summary of all your DNA health reports, covering disease risks, functional health, and performance.
Download sample report ›Your genetic blueprint, decoded.
EVA™ screens more than 200 million genetic variants through OmicsEdge and delivers 14 reports across five categories, from methylation and detox pathways to inherited cancer and medication response.

Fourteen reports. One clear picture.
What your DNA reveals, and how EVA™ acts on it.
Reads eight genes controlling folate conversion, B12 absorption, homocysteine recycling and neurotransmitter clearance.
Assesses Phase I and Phase II liver detoxification, how efficiently you process toxins, medications and waste.
Evaluates cognitive resilience and Alzheimer's risk, including full ApoE genotyping with clear risk tiers.
Weighs inherited risk for coronary artery disease and stroke against more than a million variants each.
Examines predispositions to insulin resistance, Type 2 diabetes and energy-metabolism efficiency.
Examines genetic predispositions affecting digestive function, gut lining integrity, and sensitivity to specific foods and compounds.
Assesses genetic variants influencing testosterone pathways, oestrogen metabolism, cortisol regulation, and overall hormonal balance.
Evaluates inherited tendencies toward elevated inflammatory response and immune dysregulation across key pathways.
Reads your genetic response to carbohydrates, fats and protein, plus sensitivity risk for lactose, gluten and more.
Examines muscle fibre type, VO2 max potential, recovery rate and injury susceptibility.
Aggregates inherited risk across colorectal, prostate, breast, ovarian, lung, melanoma and pancreatic cancers.
Predicts how you metabolise cardiovascular, psychiatric, pain and other drug classes, and your adverse-reaction risk.
Maps your genetic heritage across global populations, providing context for your inherited background.
Download sample report ›23 genes, one core pathway.
Methylation underpins DNA repair, detoxification, neurotransmitter synthesis and homocysteine control. Each gene is reported as normal, slightly impaired, or significantly impaired.
23 genes comprehensively analysed. The 8 most impactful genes directly shape your protocol.
Converts folate into its active form for DNA repair and homocysteine recycling. The most clinically significant methylation gene, with variants in roughly 40% of people.
Regulates absorption of natural folate from food, so variants reduce dietary folate even on a folate-rich diet.
Converts synthetic folic acid into active folate inside cells. Variants mean standard folic acid is poorly used.
Recycles homocysteine back into methionine, a key control point for homocysteine levels.
Regenerates the active B12 that MTR needs, so variants stall the cycle even when B12 looks adequate.
Controls B12 absorption from the gut, so variants cause poor uptake regardless of intake.
Activates Vitamin B6 into its functional form for homocysteine metabolism and neurotransmitter synthesis.
Controls the breakdown of dopamine, adrenaline and oestrogen, shaping the stress response and oestrogen exposure.
Alzheimer's risk, stratified.
The Alzheimer's result in the Brain Health report is driven by your ApoE genotype. EVA™ shows your allele pair and applies one of four tiers. This is a measure of genetic predisposition, not a diagnosis.
One or two protective alleles. Associated with below-average Alzheimer's risk.
Most common genotype. No E4 allele.
One risk allele.
Two risk alleles.
The most powerful genetic signal available.
Most genetic tests look at single genes. A polygenic risk score aggregates signals from hundreds of thousands of variants across your genome to calculate your true inherited risk for a specific disease. Far more accurate than any single-gene result. OmicsEdge is the only direct-to-consumer platform with clinically validated polygenic risk scores published in Nature, covering heart disease, Alzheimer's, diabetes, and seven cancer types. Your EVA™ protocol is built with these scores as a foundation.
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