24G Cross DNA
د.إ3,500.00Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks
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24G Health DNA Test – Comprehensive Genetic Health & Wellness Analysis
د.إ3,500.00The 24G Health DNA Test is a comprehensive genetic test that analyzes 24 key health-related genes to provide personalized insights into your wellness, nutrition, fitness, and disease risk. It offers actionable recommendations tailored to your DNA, helping you optimize your lifestyle, diet, and exercise routines.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks -
24G Pharmacogenomics & DNA Test – Personalized Medicine & Genetic Insights
د.إ3,500.00The 24G Pharmacogenomics plus DNA Test is a cutting-edge genetic analysis that provides personalized insights into drug response and overall health. It examines pharmacogenomics, helping to predict how your body metabolizes medications, reducing adverse drug reactions and optimizing treatment plans. Additionally, it includes a comprehensive DNA test covering traits, wellness, and genetic predispositions. Key benefits include personalized medication guidance, enhanced treatment safety, and actionable health insights.
Sample Type : Saliva
Methodology : Illumina
TAT : 3-6 Weeks -
Fragile X (FMR1) Mutation Screen (L)
د.إ3,400.00The Fragile X (FMR1) Mutation Screen (L) is a genetic test designed to detect mutations in the FMR1 gene, which are associated with Fragile X syndrome, a leading cause of inherited intellectual disability and autism. This screening identifies CGG repeat expansions, distinguishing between normal, premutation, and full mutation alleles. Key benefits include early detection for informed reproductive decisions, risk assessment for carriers, and guidance for personalized medical management. Utilizing advanced molecular techniques, the test ensures high accuracy and reliability. Ideal for individuals with a family history of Fragile X or unexplained developmental delays, this screening provides critical genetic insights for proactive healthcare planning.
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Fragile-X Syndrome Genetic Test – Accurate Lab Screening for Inherited Conditions
د.إ6,250.00Detect Fragile-X Syndrome with a lab test that identifies FMR1 gene mutations linked to intellectual disability and developmental delays.
Sample Type : Whole Blood
Methodology : Direct Mutation Analysis by PCR and Southern Blot Analysis
TAT : 30 Days -
MTRR A66G Genetic Test – Personalized Health & Methylation Analysis
د.إ1,520.00The MTRR A66G test is a genetic screening tool that identifies a specific variant (A66G) in the MTRR gene, which plays a crucial role in folate metabolism and homocysteine regulation. Key features include accurate DNA analysis, easy sample collection (typically via saliva or cheek swab), and fast turnaround time.
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NutriFit Test: Personalized DNA-Based Nutrition & Fitness Analysis
د.إ3,200.00NutriFit is a comprehensive DNA test that analyzes genetic predispositions related to nutrition, metabolism, and fitness. It provides personalized insights into nutrient absorption, food intolerances, metabolic efficiency, and optimal diet types. The test also evaluates genetic factors influencing weight management, muscle performance, and recovery, helping users tailor their diet and exercise plans for maximum effectiveness.
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PredictLife Test – Advanced DNA Health & Wellness Analysis for Personalized Insights
د.إ3,200.00PredictLife Test is a cutting-edge DNA-based health and longevity assessment that provides personalized insights into your genetic predispositions, lifestyle risks, and potential health outcomes. Using advanced AI and genomic analysis, it evaluates factors like disease risks, aging patterns, nutrition, and fitness optimization.
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SPINAL MUSCULAR ATROPHY (SMA) Test – Fast & Accurate Genetic Screening
د.إ2,000.00The **SPINAL MUSCULAR ATROPHY (SMA) Test** is a cutting-edge genetic screening tool designed to detect mutations in the **SMN1 gene**, the primary cause of SMA, a severe neuromuscular disorder. This highly accurate test enables **early diagnosis**, allowing for timely medical intervention and personalized treatment plans. It is **non-invasive**, requiring only a simple blood or saliva sample, and delivers **fast, reliable results**. Ideal for **newborn screening, carrier detection, and prenatal testing**, it empowers individuals and families with crucial genetic insights. With advanced technology ensuring **high sensitivity and specificity**, this test is a must-have for proactive healthcare and informed decision-making.