ULTIMATE PRECISION PLUS+
€680
This packages requires six tubes of blood drawn and a urine sample, given on the day.
A fasting period of 12hrs is recommended.
Please arrive at your appointment fully hydrated, drinking 500-1000ml of water first thing in the morning. This is required to provide an adequate urine sample and to make the blood draw easier.























DNA TESTING INFORMATION
Lipid Metabolism & Cholesterol Regulation
APOA2 (Apolipoprotein A2)
Regulates HDL (good cholesterol) metabolism.
Certain variants influence saturated fat sensitivity and obesity risk.
LDLR (Low-Density Lipoprotein Receptor)
Removes LDL (bad cholesterol) from the blood.
Mutations are linked to familial hypercholesterolaemia (FH).
APOB (Apolipoprotein B)
A key component of LDL; involved in cholesterol transport.
Mutations can lead to high cholesterol and heart disease.
Lactose, Gluten, & Taste Sensitivity
MCM6 (Minichromosome Maintenance Complex Component 6)
Regulates lactase production.
Variants determine lactose tolerance or intolerance in adulthood.
HLA-DQ2.5 / HLA-DQ8 (Human Leukocyte Antigen)
Genes associated with coeliac disease and gluten intolerance.
Carrying one or both variants increases risk of gluten-related disorders.
TAS1R3 (Taste Receptor Type 1, Member 3)
Influences sweet taste perception and sugar preference.
Variants affect sugar cravings and dietary choices.
TAS2R38 (Taste Receptor Type 2, Member 38)
Determines bitter taste perception, affecting sensitivity to bitter foods like broccoli and coffee.
Vitamin & Mineral Metabolism
GNB3 (Guanine Nucleotide-Binding Protein Subunit Beta-3)
Linked to sodium retention and blood pressure regulation.
Certain variants are associated with obesity and hypertension.
BCOM1 (Beta-Carotene Oxygenase 1)
Converts beta-carotene (from plants) into vitamin A.
Some variants reduce conversion efficiency, increasing the need for preformed vitamin A from animal sources.
TCN1 (Transcobalamin 1)
Regulates vitamin B12 transport and absorption.
Variants may influence B12 levels and deficiency risk.
MTHFR (Methylenetetrahydrofolate Reductase)
Involved in folate metabolism and homocysteine regulation.
Mutations can increase risk for heart disease, neural tube defects, and methylation issues.
SLC23A1 / SLC23A2 (Solute Carrier Family 23, Member 1 & 2)
Regulate vitamin C transport and absorption.
Variants may affect plasma vitamin C levels and antioxidant protection.
GC (Group-Specific Component, aka Vitamin D Binding Protein)
Binds and transports vitamin D in the bloodstream.
Variants can affect vitamin D status and bone health.
CYP2R1 (Cytochrome P450 Family 2 Subfamily R Member 1)
Converts vitamin D into its active form.
Variants may affect vitamin D levels and deficiency risk.
TRPM6 (Transient Receptor Potential Cation Channel Subfamily M Member 6)
Involved in magnesium absorption.
Variants can increase the risk of magnesium deficiency and high blood pressure.
SEP-15 (Selenoprotein 15)
Plays a role in selenium metabolism and antioxidant defence.
Variants may impact cancer risk and immune function.
CA1 (Carbonic Anhydrase 1)
Involved in pH balance and hydration.
Variants may influence fluid retention and electrolyte balance.
LRP5 (Low-Density Lipoprotein Receptor-Related Protein 5)
Regulates bone mineral density.
Mutations can increase or decrease bone strength.
Omega-3 & Fatty Acid Metabolism
FADS1 / FADS2 (Fatty Acid Desaturase 1 & 2)
Regulate conversion of ALA (plant-based omega-3) into EPA & DHA.
Variants determine how well you process omega-3 & omega-6 fatty acids.
Fitness, Strength, & Muscle Genes
MSTN (Myostatin)
Regulates muscle growth inhibition.
Variants with reduced function may increase muscle mass and strength.
ACTN3 (Alpha-Actinin-3)
Known as the "sprinter gene", influencing fast-twitch muscle performance.
Variants determine power vs. endurance athletic potential.
AGTR2 (Angiotensin II Receptor Type 2)
Plays a role in blood pressure regulation and endurance performance.
IL-6 (Interleukin-6)
Affects inflammation and muscle recovery.
Variants may influence exercise recovery and immune function.
COL5A1 (Collagen Type V Alpha 1 Chain)
Affects ligament strength and injury risk.
Certain variants increase risk for Achilles tendon injuries.
CKM (Creatine Kinase, Muscle Type)
Involved in energy production for muscle contraction.
Variants can impact muscle endurance and recovery speed.
Obesity, Metabolism, & Appetite Genes
FTO (Fat Mass and Obesity-Associated Protein)
Strongest genetic predictor of obesity.
Variants influence hunger, calorie intake, and fat storage.
MC4R (Melanocortin 4 Receptor)
Regulates appetite and energy balance.
Mutations can lead to increased hunger and obesity.
SLC30A8 (Solute Carrier Family 30, Member 8)
Involved in insulin secretion.
Variants influence Type 2 diabetes risk.
TCF7L2 (Transcription Factor 7-Like 2)
One of the strongest genetic risk factors for Type 2 diabetes.
ADD1 (Adducin 1)
Regulates sodium balance and blood pressure.
Certain variants may increase salt sensitivity & hypertension risk.
Caffeine, Sleep, & Mood Regulation
CYP1A2 (Cytochrome P450 1A2)
Determines caffeine metabolism speed (fast vs. slow metaboliser).
ADORA2A (Adenosine A2A Receptor)
Affects caffeine sensitivity and sleep quality.
CLOCK (Circadian Locomotor Output Cycles Kaput)
Regulates circadian rhythm and sleep patterns.
GABRA6 (Gamma-Aminobutyric Acid Type A Receptor Subunit Alpha6)
Affects stress response and anxiety.
HTR1B (5-Hydroxytryptamine Receptor 1B)
Regulates serotonin signalling; linked to mood and impulsivity.
NPAS2 (Neuronal PAS Domain Protein 2)
Works with CLOCK gene to regulate sleep-wake cycles.