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Q: 🧬 NIFTY Non-Invasive Prenatal Testing

NIFTY Non-Invasive Prenatal Testing Non-Invasive Prenatal Testing for detecting fetal chromosomal aneuploidies from maternal blood, such as Down syndrome, Edward syndrome, and Patau syndrome Target customer: pregnant women GA 10 – 24 weeks Package: NIFTY pro, NIFTY core, NIFTY focus, NIFTY twin Specimen: blood 10 ml Streck tube TAT: 5-7 working days Method: NGS (low-pass WGS)

Discover how your genes influence your health—and take control. MedEx’s advanced genetic testing and analysis deliver precise, actionable insights to optimise your wellness today and for the future.

Personalised. Proactive. Powerful.

✅ Comprehensive testing, actionable insights and expert-led consultation
✅ Easy to understand illustrative reports with recommendations sent straight to your inbox
✅ Secure, private and confidential screening
✅ Clinician assisted specimen collection at network facilities or at an on-demand location

Walk-ins welcome at MedEx, Sukhumvit 13, Bangkok

Open Daily 8am-10pm. 2 Minutes Walk from BTS Nana, BTS Asok and MRT Sukhumvit.

*Get your test at home or hotel for an extra 750 baht only, a clinician can be at your location within 1 to 3 hours.

Unlocking the Secrets of Your DNA

Explore Your Ancestry, Optimize Your Health, and Embrace Your Unique Genetic Traits with Our Comprehensive DNA Testing Service

Unlock Your Genetic Blueprint

Discover the secrets hidden within your DNA. It holds the key to your past, present and future. We're here to help you decode it.

Health Recommendations

Get personalised insights based on your unique DNA, helping you make informed decisions about your health and lifestyle.

Insight into Your Biological Age

Help identify whether your body is aging faster or slower than expected. Can reveal factors influencing your longevity and health.

Genetic Wellness Roadmap

Get a roadmap for a healthier future, complete with actionable steps to optimize your well-being.

Empower Your Choices

Understand your genetic predispositions and make choices that align with your unique genetic makeup.

Confidential & Secure Testing

Rest easy knowing your DNA data is kept confidential and secure, following strict industry standards for privacy.

How It Works

A Step-by-Step Guide to Understanding the Process

Book Your Test Submit the Booking Form on this page or contact us for reservation. You can walk-in to MedEx Neo Clinic or get the kits delivered. Clinician assisted specimen collection service is available.

1. Book Your Test Convenient Scheduling — Submit the Booking Form on this page or contact admins for reservation. You can walk-in to MedEx Neo Clinic, Sukhumvit 13, Bangkok or get the kits delivered. Clician assisted specimen collection service is available.

Specimen Collection Most DNA Tests require Swab Specimen. MedEx can deliver the self-collection kits internationally. For DNA Tests requiring blood specimen visit us or utilise our at-home clinician assisted specimen collection service throughout Thailand.

2. Collect Specimen Easy Sample Collection — Most of the DNA Tests require Swab Specimen. As such we can deliver the Self-collection Kits internationally. For the DNA Tests requiring blood specimen you can visit us or utilize our at-home clinician assisted specimen collection service throughout Thailand.

Kit Registration While some of the available tests are processed locally, many of the specimens are sent overseas for processing. To streamline the logistics and chain of custody, most of the tests require kit registration as well as documentation. A stringent chain of custody is maintained.

3. Kit Registration and Chain of Custody While many of the available tests are processed locally, some of the specimens are sent overseas for processing. To streamline the logistics and chain of custody, most of the tests require kit registration as well as documentation.

Online Results Results in English are emailed. Reports are illustrative and easy to interpret. Some reports are made available via mobile apps. Geneticists are available for interpretation and lifestyle recommendations.

4. Online Results and Geneticist Consult Results in English are emailed. Generally the reports are illustrative and easy to interpret. Some of the test reports are very large to be shared by email — such reports are made available via a secure mobile application. Geneticists and related specialists are available for interpretation.

FEATURED TEST PACKAGE

DNA STORY

PREMIUM 500+ DNA REPORTS PROGRAM

With DNA Methylation Tests of MTHFR, MTR, MTRR, COMT and BHMT Genes

Embark on a transformative journey of self-discovery with DNA Story Premium DNA 500+ Reports Package that also includes Methylation Tests of MTHFR, MTR, MTRR, COMT and BHMT Genes.

—>SAMPLE REPORT ABOVE<—

Unlock over 500 genetic insights, unraveling the mysteries of your health and innate talents. Tailored for all ages, the package empowers you to make informed decisions for a healthier and more fulfilling life. Embrace the power of your DNA with our cutting-edge analysis and embark on a path to optimized well-being and self-awareness. Your DNA Story awaits.

PACKAGE INCLUDES:

1. Methylation Test

Methylation is a fundamental biochemical process that involves the addition of methyl groups to various molecules, including DNA, proteins, and neurotransmitters. Methylation plays a vital role in gene expression, detoxification, energy production, and neurotransmitter balance. A Methylation Test assesses genetic variations that can impact an individual’s methylation capacity. Key components covered by a Methylation Test may include:

MTHFR Gene: The methylenetetrahydrofolate reductase (MTHFR) gene is a key player in folate metabolism and methylation. Variations in this gene can affect how the body processes and utilizes folate.
MTR and MTRR Genes: These genes are involved in the conversion of homocysteine to methionine, a process crucial for methylation. Variations may impact this conversion and influence overall methylation status.
COMT Gene: The catechol-O-methyltransferase (COMT) gene regulates the breakdown of catecholamines, including dopamine, norepinephrine, and epinephrine. Genetic variations in COMT can influence neurotransmitter balance.
BHMT Gene: The betaine-homocysteine methyltransferase (BHMT) gene is involved in an alternative pathway for homocysteine metabolism.

2. Health and Nutrition: Vitamin B6, Vitamin B9 – Folate, Vitamin B12, Vitamin C, Vitamin A, Vitamin D, Omega-3 fatty acids, Copper, Phosphorus, Caffeine sensitivity, Alcohol sensitivity, Calcium, Magnesium, Zinc, Nutrition, Lactose intolerance, Celiac predisposition, Response to saturated fat, Satiety – obesity gene, Liver detoxification, Spice sensitivity, Sweet tooth, Cellular detoxification, Salt sensitivity.

3. Allergy and Sensitivity: Cockroach allergy, Dust mite allergy, Pet allergy, Atopic dermatitis, Spice sensitivity.

4. Talent and Abilities: Reading and spelling ability, Language, Musical Ability, Pollen allergy, Intelligence, Mathematical ability, Working memory, Memory ability, Multi-tasking skills, Power sports, Task attention, Creativity, Endurance sports.

5. DNA Character: Adventurer, Adjuster, Analyst.

6. Fitness and Sports Performance: VO2 Max – Aerobic potential, Injury risk, Power/Endurance potential, Free radicals during exercise, Post-exercise recovery, Insulin sensitivity response to exercise, HDL response to exercise, Glucose response to exercise.

7. Healthy Weight: Low-carb diet, Low-calorie diet, Low-fat diet, Cardio exercise, Strength training.

8. COVID-19 Infection and Severe Symptoms Risk: ABO gene, OAS gene, DDP9 gene.

9. Behavioral Traits: Addictive Behavior, CCHCR1 gene.

10. Personality Traits: Intrinsic Motivation to Exercise, Misophonia, Stress management.

11. Skin and Beauty: Age Spots, Skin Glycation Risk, Morning Person, Freckles, Acne Risk, Stretch Marks, Wrinkles, Keloid Formation, Sun Sensitivity, Cellulite Protection.

12. Sleep and Environmental Sensitivity: Sleep duration, Deep sleep, Sleep movement, Air pollution, Pollution Sensitivity, Secondhand smoke, Traffic-related pollution.

13. Neurological and Mental Health: Alzheimer’s disease, Age-related macular degeneration, Health Risk, Parkinson’s disease, Hereditary thrombophilia, Hereditary hemochromatosis, Elevated Triglycerides, Type 2 Diabetes, Androgenetic alopecia, Body odor, Elevated LDL Cholesterol, Decreased HDL Cholesterol, Hypertension.

14. Physical Traits: Bitter taste sensitivity, Earwax type, Hair thickness, Pain sensitivity, Motion sickness, Age-related hearing loss.

15. Carrier Status: Achondrogenesis, Acute fatty liver, Alpha-Mannosidosis, Agenesis of the Corpus Callosum with Peripheral Neuropathy, Achromatopsia, Alkaptonuria, ARSACS, Autosomal Recessive Polycystic Kidney Disease, Andermann syndrome, Bloom syndrome, Bardet-Biedl Syndrome, Beta-sacroglycanopathy (Limb-girdle muscular dystrophy), Carnitine Palmitoyltransferase deficiency, Citrullinemia type I, Cohen syndrome, Congenital Adrenal Hyperplasia, Cystic fibrosis, Deafness, Dihydrolipoamide Dehydrogenase deficiency, Duchenne Muscular Dystrophy, Familial Dysautonomia, Beta Thalassemia & related hemoglobinopathies, Biotinidase deficiency, Galactosylceramide beta-galactosidase deficiency, Caravan Disease, Choroideremia, Citrullinemia type II, Combined Pituitary Hormone Deficiency, Congenital Disorder of Glycosylation, D-Bifunctional Protein Deficiency, Diastrophic Dysplasia, Dilated Cardiomyopathy, Factor XI Deficiency, Familial Mediterranean fever, Fanconi Anemia, Gaucher Disease, Glutaric acidemia, Glycogen storage disease type 1a, Glycogen storage disease type V, Hereditary Fructose Intolerance, Hexosaminidase A Deficiency (Including Tay Sachs Disease), Homocysteinemia, Inclusion Body Myopathy, Joubert Syndrome, Leigh Syndrome, French Canadian Type, Limb-Girdle Muscular Dystrophy Type 2E, Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD), Maple Syrup Urine Disease Type 1A, Mucolipidosis, Methylmalonic Acidemia, Muscular dystrophy-dystroglycanopathy, Neuronal Ceroid Lipofuscinosis, Northern Epilepsy, Pendred Syndrome, Pompe Disease, Pseudocholinesterase Deficiency, Primary Hyperoxaluria type III, Rhizomelic Chondrodysplasia Punctata Type 1, Sickle Cell Anemia, Familial Hyperinsulinism, G6PD, GRACILE syndrome, Glycogen storage disease type 1b, Hemophilia B, Herlitz Junctional Epidermolysis Bullosa, Homocystinuria, Hyperinsulinism, Isovaleric Acidemia, Krabbe Disease, Limb-Girdle Muscular Dystrophy Type 2D, Limb-Girdle Muscular Dystrophy Type 2I, Maple Syrup Urine Disease Type 1B, Maple Syrup Urine Disease Type III, Metachromatic Leukodystrophy, Mucopolysaccharidosis, Nemaline Myopathy, Niemann-Pick Disease, Oculocutaneous Albinism, Polyglandular Autoimmune Syndrome, Primary Carnitine Deficiency, Primary Hyperoxaluria type II, Pycnodysostosis, Salla Disease, Sjogren-Larsson Syndrome, Tyrosinemia Type I, Usher Syndrome type 1F, Usher Syndrome type 3A, Zellweger Syndrome Spectrum.

16. Ancestry: For this report, the program will analyze genes to identify DNA similarities based on populations of each race collected from around the world.

17. DNA Fun Facts: Asparagus Odor Detection, Romantic relationship status.

18. Cancer Risk: Breast Cancer, Colorectal Cancer, Pancreatic Cancer, Prostate Cancer, Gastric Cancer, Ovarian Cancer, Lung Cancer, Skin Cancer, Urinary Bladder Cancer, Cervical Cancer, Melanoma Cancer.

19. Premium Health Risk: Osteoarthritis, Osteoporosis, Periodontitis, Telomere length, Lipoprotein a or Lp(a), Glaucoma, Gallstones, Varicose veins, Migraine, Systemic Lupus Erythematosus (SLE), Anxiety, Asthma.

20. Drug Response: Cardiovascular drugs, Anti-inflammatory drugs, Antibacterial drugs, Antifungal drugs, Antiviral drugs, Skeletal Muscle Relaxants, Antidepressant drugs, Sedative drugs, Gastrointestinal drugs, Antipsychotic drugs, Immunological drugs, Anticonvulsant drugs, Antineoplastic drugs, Antiemetics drugs, and Antigout drugs.

21. Heart Diseases: This test analyzes genes related to various types of genetically inherited heart diseases within the family, such as severe heart muscle disease, severe heart arrhythmias, and severe hyperlipidemia.

22. Brain Disorders: This test analyzes genes related to brain and nervous system diseases that are inherited genetically.

23. Cardiovascular Disease Risk: This test analyzes genes involved in various inherited cardiovascular diseases: Stroke, Coronary artery disease, Atherosclerosis.

24. Genetic Height: This report will analyze genes related to growth and hormone production, which constitute factors influencing an individual’s height. The results of your genetic analysis will be utilized to estimate your height based on the average height for your race.

25. Detoxification DNA Test: Detoxification DNA Test analyzes specific genetic markers associated with the body’s detoxification processes. The human body has sophisticated mechanisms to eliminate toxins and harmful substances, and these processes are influenced by various genes. The Detoxification DNA Test provides insights into how efficiently an individual’s body processes and removes toxins, pollutants, and other environmental stressors.

🧬 DNALL Prestige (700+ Reports) and SNIP & PICK (500+ Reports)

Examining the genetic code to analyze individual characteristics lifestyle, design balancing food and nutrition including the exercise that is most appropriate for you. It can also predict the risk of diseases that will be caused by genetic factors to be used as information to reduce the risk of disease in the future.

🧬 Prenatal and Postnatal Paternity Test

Non-Invasive Prenatal Paternity Test (NIPPT)

Confirm the paternity of your unborn baby with a 99.9% accurate test that requires only blood samples from the mother and alleged father

🧬 NIFTY Non-Invasive Prenatal Testing

NIFTY Non-Invasive Prenatal Testing

Non-Invasive Prenatal Testing for detecting fetal chromosomal aneuploidies from maternal blood, such as Down syndrome, Edward syndrome, and Patau syndrome

🧬 VISTA Carrier Screening

VISTA Carrier Screening

Carrier screening for Monogenic disease

vist

Target customer: couples who are planning for pregnancy, during pregnancy before GA 14 weeks
Package: Mini panel - 12 โรค Targeted panel 2.0 - 173 โรค
Specimen: blood 5 ml EDTA tube
TAT: 21 working days
Method: NGS (Target region capture)

VISTA Thalassemia-Seq

Thalassemia mutations detection for > 508
Thalassemia mutation including common
Alpha- and Beta-thalassemia

🧬 NOVA Newborn Genetic Testing

NOVA Newborn Genetic Testing

Newborn genetic screening for 112 genetic diseases.

NOVA Newborn Metabolic Screening

Newborn 48 metabolic disorders screening

🧬 BGI Xome: Whole Exome Sequencing for Rare Diseases Diagnosis

Clinical whole exome sequencing for detection and diagnosis of rare diseases

🧬 COLOTECT - Early Screening of Colorectal Cancer

COLOTECT is a non-invasive colorectal cancer (CRC) screening test offered by Bangkok Genomics Innovation. It detects abnormal DNA methylation in stool samples, specifically targeting genes associated with CRC. The test boasts a sensitivity of 89.47% and a specificity of 93.55% for detecting colorectal cancer, and a 42% sensitivity for identifying advanced adenomas, which are precancerous lesions.

Designed for individuals aged 45 and above, as well as health-conscious individuals seeking CRC screening, COLOTECT offers a user-friendly approach. Users can collect stool samples at home without the need for dietary restrictions or special preparations, making the process convenient and private. The samples are then sent to a laboratory for analysis, with results typically available within seven working days.

By identifying DNA methylation changes, COLOTECT can detect colorectal cancer even in its early stages, before symptoms appear. This early detection is crucial for effective treatment and improved survival rates. The test's non-invasive nature and high accuracy make it a valuable tool for colorectal cancer screening.

🧬 SENTIS Hereditary Cancer Screening

SENTIS Hereditary Cancer Screening

Detection of gene mutations that result in a higher-than-normal chance of developing cancer which can help predict the risk of cancer.

🧬 Gut Microbiome DNA Test By GC Genome

Do you experience symptoms of gut microbiome imbalance?

Signs may include:

Bloating, diarrhea, or constipation
Persistent inflammatory acne
Recurring allergic rashes
Difficulty with weight loss

Did you know that the gut houses over 5,000 types of microorganisms? Our Gut Microbiome Screening examines more than 100 different microorganisms in your body.

This screening uses stool samples to evaluate gut bacteria, providing key insights into:

Levels and diversity of over 100 gut microbiota species
Their potential links to various health conditions, including:
Obesity
Chronic irritable bowel syndrome
Diabetes
High cholesterol
Cardiovascular issues related to meat consumption
Colon polyps
Depression
Rheumatoid arthritis
Age-related macular degeneration

Importance of Gut Microbiome Screening

A balanced gut microbiome supports a protective mucus layer that guards against harmful bacteria and inflammation. An imbalance may elevate the risk of diseases such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS), and increase susceptibility to conditions triggered by pathogenic bacteria.

How the Test is Conducted

The test involves Next Generation Sequencing (NGS) and uses a swab similar to an ATK test. It can be completed at home or in the hospital. If done at home, a hospital staff member will collect the swab and send it to Korea for analysis. The process is quick and straightforward.

Benefits of the Screening

Identify the types, abundance, and roles of gut microbiota
Assess the variation among different microbiota species
Receive customized recommendations for enhancing gut health, including dietary and lifestyle changes

Next Steps After Results

A doctor will interpret your results, assess your risk for conditions related to gut microbiota, such as IBS, obesity, diabetes, migraines, anxiety, and depression. They will offer advice on:

Diet modifications to boost healthy microorganisms, including increased intake of probiotics and prebiotics
Lifestyle adjustments, such as improved sleep, regular exercise, and dietary changes

Recommendations for a Healthy Gut

Aim for 6–8 hours of sleep each night to support gut health
Engage in at least 30 minutes of exercise 3–5 times a week
Minimize processed meats, spicy, salty, and rich foods
Incorporate a diet rich in probiotics and prebiotics to maintain a healthy gut microbiome

Who Should Consider This Screening?

This screening is suitable for individuals with symptoms such as:

Digestive issues (bloating, nausea, diarrhea, constipation)
Migraines or sleep problems
Persistent acne and allergic rashes
Asthma or impaired metabolic function
Mental health concerns (anxiety, depression)
Bad breath, mucus in stools, or chronic fatigue
Prolonged use of antibiotics or antacids

Preparing for the Screening

No fasting is required before the test
Avoid antibiotics for 3 days prior to screening

CONTACT MEDEX TEAM

24/7 HELPLINE

+66-025-44-0001

MEDEX NEO CLNIC

The Trendy Office Building, 1st Floor (Floor 1A, In front of the elevator), Sukhumvit 13, Khlong Toei Nuea, Watthana, Bangkok,Thailand 10110
(2-5 Min Walk from BTS Nana, BTS Asoke and MRT Sukhumvit)

Open 8 AM - 10 PM Everyday (Walk-ins Welcome)

EMAIL SUPPORT

mail@medex.co.th

Doctors On Demand

Express In-Person and Online Doctor Consultations

Immediate medical care will be provided if your test results are positive. Enjoy stress-free doctor consultations at MedEx Neo Clinic with prices starting from just 750 THB.

You can also access a pool of over 3,000 top specialists at JCI (US)-accredited Thai hospitals in the MedEx Network via our tele-consultation services.

Additionally, we offer doorstep delivery of essential healthcare supplies.

Transform Your Health with Methylation Insights

Harness the power of methylation insights to transform your health. Our advanced testing technology identifies specific methylation markers in your DNA, providing actionable data that can guide your health and lifestyle choices. Empower yourself with the knowledge to optimize your health.

Have you ever wondered why does a liver cell act differently from a brain cell if they both contain the same DNA? The answer lies in epigenetics—a layer of instructions on top of your genetic code that controls gene activity. One of the most important epigenetic mechanisms is DNA methylation, a tiny chemical tag that can silence genes without changing the DNA sequence itself.

So what exactly is methylation, and how can it impact your well-being? Let’s break it down in simple terms.

What is DNA Methylation?

DNA methylation is a natural biochemical process that acts like a “switch” for your genes. Imagine your DNA as an instruction manual for your body. Methylation is like adding tiny “on/off” tags to certain parts of that manual, telling your cells which genes to activate or silence¹.

When methylation works properly, your body functions smoothly. But when it’s disrupted, it can contribute to health issues.

Why Does DNA Methylation Matter?

1. Cell Identity & Development

Every cell in your body has the same DNA, but methylation patterns help determine whether a cell becomes a skin cell, a heart cell, or a neuron.
During embryonic development, methylation patterns are erased and rewritten to allow cells to specialise.

2. Disease & Aging

Abnormal methylation can lead to diseases like cancer (where tumor suppressor genes are silenced).
As we age, methylation patterns change, which may contribute to aging-related diseases.

3. Environmental Influence

Diet, stress, toxins, and lifestyle (like smoking) can alter methylation patterns, affecting health.
This is why identical twins, despite having the same DNA, can develop different diseases over time.

How does Methylation affect your body?

Methylation impacts nearly every system in your body. Here’s how:

1. Energy & Metabolism

Helps convert food into energy
Supports detoxification (removing harmful substances)

2. Brain & Mood

Influences neurotransmitter production (like serotonin and dopamine)
Affects mental clarity, stress response, and mood regulation

3. Immune System

Helps control inflammation
Supports immune cell function

4. Aging & Longevity

Methylation patterns change with age and can influence cellular aging.

When methylation is imbalanced, it may contribute to:

Fatigue
Mood disorders (anxiety, depression)
Hormonal imbalances
Chronic inflammation
Increased risk of certain diseases

Who can benefit from DNA Methylation Testing?

Methylation testing isn’t for everyone, but it can be incredibly helpful if you:

✔ Struggle with chronic fatigue or low energy
✔ Have a family history of heart disease, cancer, or neurological conditions
✔ Experience mood disorders (anxiety, depression)
✔ Have digestive issues or autoimmune conditions
✔ Want to optimise longevity and wellness

Testing can uncover whether your methylation pathways are functioning properly and guide personalised treatment plans.

How does DNA Methylation Testing work?

There are different types of tests², but most involve a simple blood, saliva, or cheek swab sample. Here’s what they look for:

1. Global Methylation Testing

Measures overall methylation patterns in your DNA
Helps identify general imbalances

2. Gene-Specific Methylation Testing

Focuses on specific genes linked to health conditions
Can reveal risks for heart disease, cancer, or mental health issues³

3. Functional Methylation Panels

Evaluates nutrient levels (like Folate, B12) that support methylation
Checks for homocysteine levels (a marker linked to heart and brain health)
Once your results are in, our partnered providers can help you interpret them and recommend personalised lifestyle, diet, or supplement strategies to support optimal methylation.

Is Methylation Testing right for you?

DNA methylation is a powerful process that affects nearly every aspect of your health. If you’ve been dealing with unexplained fatigue, mood issues, or chronic conditions, methylation testing could provide valuable insights.

At MedEx, we’re proud to partner with leading providers to offer DNA methylation testing—a cutting-edge way to understand your genetic health.

Key sources

Variants in the genome affect DNA methylation by deCODE Genetics ↩︎
DNA Methylation Analysis: Choosing the Right Method ↩︎
New findings showing how DNA methylation influences diseases (National Library of Medicine) ↩︎

FAQs

Frequently Asked Questions

Is Genetic Testing accurate?

Genetic testing is generally very accurate, but not always perfect.

The accuracy of a test can depend on the specific condition being tested for, the type of test used, and the laboratory performing the test.
Genetic testing can't always tell you if you'll develop a disease, how severe it will be, or how it will progress.

In a nutshell, genetic testing can be a valuable tool for understanding genetic risks, but it's crucial to interpret the results cautiously and understand the limitations of the tests, especially for complex conditions. Always consult your doctor for interpretation.

Is Genetic Testing safe?

Genetic testing is generally considered safe, especially when involving blood or cheek swab samples, and pose very minimal physical risks. However, there can be emotional, social, and financial implications associated with genetic testing, that should be considered. Always address any concerns with your doctor.

What are Genetic Disorders?

Genetic disorders arise due to alterations in an individual's genetic material, encompassing their genes and chromosomes. Aneuploidy characterizes a condition where there are either surplus or deficient chromosomes. Trisomy denotes the presence of an extra chromosome, while monosomy signifies the absence of one chromosome. Inherited disorders, conversely, result from genetic changes termed mutations. These disorders comprise conditions like sickle cell disease, cystic fibrosis, Tay-Sachs disease, and numerous others. Typically, for an offspring to be affected by an inherited disorder, both parents must carry the same mutated gene.

What other Genetic Testing do you have available?

Our list of availability is continuously evolving, please see our booking form, but please find below the main categories of tests available:

Hereditary Cancer and Carrier Screening for familial health risks
Pharmacogenetics for medication compatibility
Ancestry Insights to uncover your genetic heritage
Whole Exome Sequencing for detailed genetic analysis
Gut Microbiome Genetic Testing for digestive health insights
NIPT/NIPS Screening for baby's gender and genetic abnormalities
Pre- and Postnatal Paternity Testing for parental verification
VISTA Pre-Pregnancy Genetic Testing for planning a healthy family
NIFTY Fetal Genetic Health Assessment for advanced prenatal care
Genetic Blueprint Testing to unlock your DNA's potential and identify predispositions
COLOTECT Colon Cancer Screening for early detection

Venture into Your DNA

Discover your Genetic Blueprint, Enhance Health, and Prepare for Parenthood

1. Comprehensive Genetic Testing

Genetic testing is a broad category of medical and scientific examinations that involve analyzing an individual's DNA. These tests can reveal information about an individual's genetic makeup, including their susceptibility to certain diseases, ancestry, and genetic traits. Genetic testing has applications in various fields, such as medicine, ancestry research, and personalized healthcare. It helps individuals and healthcare providers make informed decisions regarding health, family planning, and overall well-being.

1. VISTA Pre-Conception Health Check Test For Genetic Disorders

This is a medical test that couples or individuals planning to have a baby can undergo before conception. It is designed to identify potential genetic disorders in the baby's DNA. The primary goal is to provide reliable and early information about the fetal genetic health without resorting to invasive procedures that might carry the risk of miscarriage. This test helps parents make informed decisions about their pregnancy and prepares them for any potential health challenges their child may face.

2. SENTIS Hereditary Cancer Screening

SENTIS Hereditary Cancer Screening is a specialized DNA test that focuses on detecting genetic mutations associated with hereditary or familial cancers. This test helps individuals understand their genetic predisposition to certain types of cancer. By analyzing an individual's genetic blueprint, SENTIS aims to provide early insights into the risk of developing hereditary cancers. Armed with this knowledge, individuals can take proactive measures for cancer prevention and early detection, potentially saving lives.

3. DNALL Hereditary DNA Testing to Discover Your Genetic Blueprint

Hereditary DNA testing is a comprehensive examination of an individual's genetic makeup. By analyzing an individual's DNA, this test offers insights into one's unique genetic blueprint. It can reveal information about ancestry, traits, and potential health risks, including genetic predispositions to various conditions. This test empowers individuals to gain a deeper understanding of themselves on a genetic level, which can be valuable for making informed decisions about their lifestyle, health, and wellness.

Last updated: June 30th, 2022

If you’re dissatisfied with a purchase, We invite You to read our refund and return policy. The following conditions apply to any items or services that you bought from Us.

Interpretation and Definitions

1. Interpretation

The meanings of words with the first letter capitalized are defined as follows. The following definitions shall have the same meaning regardless of whether they appear in singular or plural.

2. Definitions

For the purposes of this Refund and Return Policy:

Company (referred to as either “the Company”, “We”, “Us” or “Our” in this Agreement) refers to MedEx Ventures Co., Ltd., 10-95/97 Trendy Building, 6th Floor, Soi Sukhumvit 13 Sukhumvit Road, Khlong Toei Nuea, Watthana, Bangkok 10110.
Service refers to the Website
Packages are the medical and non-medical assistance provided by Our facilities or Our partner providers’ facilities as part of the Service, such as appointments and treatments scheduled on the Service that may be redeemed at either.
Goods refer to the physical items offered for sale on the Service.
Orders are any paid requests made by You to acquire Products or Packages from Us.
Website refers to MedEx portal accessible from https://medex.co.th
You means the individual accessing or using the Service, or the company, or other legal entity on behalf of which such individual is accessing or using the Service, as applicable.

3. Your Order Cancellation Rights

You are entitled to cancel Your Order for Packages as per the following terms:

3.1 If you cancel an Order before 4 PM (GMT+7) the next day after making the payment, you can receive an 80% refund. For example, if you want to cancel your reservation, for example, after making it on March 25th, 2022 at 10 AM; You may do so and receive an 80% refund if you notify the company before 4:00 PM on March 26th, 2022.

3.2 If you cancel an Order before 4 PM (GMT+7) one day before the appointment date, you will receive a 50% refund. For example, if you scheduled a lab test for March 29th at 10 AM, you may cancel and receive a 50 percent refund if you notify the laboratory by 4 PM on March 28th, 2022.

3.3 The refund is not allowed if you cancel the order after 4 PM (GMT+7) one day before the appointment date.

3.4 In case the refund request time is both before 4 PM (GMT+7) the next day after making the payment and before 4 PM (GMT+7) one day before the appointment date, the condition for the latter will be applicable.

3.5 If You request a Full Refund and submit a medical certificate certifying that the Package is not fit for You due to an unforeseen medical condition, the Company can give You a complete refund.

3.6 If our partner shop, clinic, or hospital is unable to provide Packages to customers who have paid for them, the Company can give a full refund.

3.7 We cannot return payments made directly to our partner service. If you are dissatisfied with the service provided by our partners, please contact us at support@medex.co.th with a statement of your issue. We will escalate the complaint to the provider in an attempt to address the problem and take necessary actions.

Take note that the Company will request for cancellation reasons or other causes so we may improve our service.

The deadline for canceling an Order for Goods is 7 days after you receive the product or at which a third party you have designated, who is not the carrier, takes possession of the goods delivered.

To exercise Your right of cancellation, You must notify Us in writing. You can inform us of your decision by:

By submitting the refund request form at https://medex.co.th/refund
By email: mail@medex.co.th

4. Refund Timeframe

We will refund You within 45-60 days from the appointment date for Packages or the day We receive the returned items in the case of Goods. We’ll use the same payment method as you used for your Order, and you may be charged additional fees as a result. Refunds are subject to the transaction and exchange fees.

5. Returning Goods

You are responsible for the cost and risk of returning the Goods to Us. You should send the Goods at the following address:

MedEx Ventures Co., Ltd, 10-95/97 Trendy Building, 6th Floor, Soi Sukhumvit 13 Sukhumvit Road, Khlong Toei Nuea, Watthana, Bangkok 10110

We cannot be held responsible for Goods damaged or lost in return shipment. Therefore, We recommend an insured and trackable mail service. We are unable to issue a refund without actual receipt of the Goods or proof of received return delivery.

6. Gifts

If the Goods were marked as a gift when purchased and then shipped directly to you, You will receive a gift credit for the value of your return. Once the returned product is received, a gift certificate will be mailed to You.

If the Goods weren’t marked as a gift when purchased, or the gift giver had the Order shipped to themselves to give it to You later, We will send the refund to the gift giver.

7. Conditions for Returns

For the Goods to be eligible for a return, please make sure that:

The Goods are in the original packaging and not used or damaged
The Goods must have the receipt or proof of purchase

The following Goods cannot be returned:

The supply of Goods made to Your specifications or clearly personalized.
The supply of Goods which according to their nature are not suitable to be returned, deteriorate rapidly or where the date of expiry is over.
The supply of Goods that are not suitable for return due to health protection or hygiene reasons and were unsealed after delivery.
The supply of Goods which are, after delivery, according to their nature, inseparably mixed with other items.

We reserve the right to refuse returns of any merchandise that does not meet the above return conditions at our sole discretion.

Contact Us

If you have any questions about our Returns and Refunds Policy, please contact us:

By email: mail@medex.co.th
By visiting this page on our website: https://medex.co.th/contact
By phone number: +66023284866
By mail: MedEx Ventures Co., Ltd, 10-95/97 Trendy Building, 6th Floor, Soi Sukhumvit 13 Sukhumvit Road, Khlong Toei Nuea, Watthana, Bangkok 10110

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