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Proteomics Testing Request #21804 | Pyae Phyo Aung - work.pyaephyoeaung@gmail.com | Proteomis™ 5-Disease Risk Forecast Test | Results in 30 - 45 days | 5̶,9̶0̶0̶0̶ T̶H̶B 39,000 THB in Test At MedEx Neo Clinic | | Appointment Requested for 02-11-2026
1 × ฿39,000.00 
Wegovy (Semaglutide) Weight Loss Injection - 0.25 mg
1 × ฿11,499.00 Subtotal: ฿50,499.00
Proteomics Testing Request #21804 | Pyae Phyo Aung - work.pyaephyoeaung@gmail.com | Proteomis™ 5-Disease Risk Forecast Test | Results in 30 - 45 days | 5̶,9̶0̶0̶0̶ T̶H̶B 39,000 THB in Test At MedEx Neo Clinic | | Appointment Requested for 02-11-2026
1 × ฿39,000.00 Wegovy (Semaglutide) Weight Loss Injection - 0.25 mg
1 × ฿11,499.00 Subtotal: ฿50,499.00
Proteomics Testing Request #21804 | Pyae Phyo Aung - work.pyaephyoeaung@gmail.com | Proteomis™ 5-Disease Risk Forecast Test | Results in 30 - 45 days | 5̶,9̶0̶0̶0̶ T̶H̶B 39,000 THB in Test At MedEx Neo Clinic | | Appointment Requested for 02-11-2026
1 × ฿39,000.00 Wegovy (Semaglutide) Weight Loss Injection - 0.25 mg
1 × ฿11,499.00 Subtotal: ฿50,499.00
Transform your health journey with advanced genetic testing services designed for personalized insights and proactive care. At MedEx, we go beyond ordinary testing to provide a comprehensive view of your DNA and its impact on your health and future.
Featured Genetic Tests: DNA Methylation. NIPT/NIPS. Paternity Test. Hereditary Cancer and Carrier Screening. Health Risks Assessment. Pharmacogenetics. Ancestry Insights. Whole Exome Sequencing. Epigenetics. Gut Microbiome.
✅ Comprehensive Testing, Actionable Insights and Expert-Led Consultations
✅ Easy-to-understand Illustrative Reports with Actionable Recommendations Straight to Your Inbox
✅ Secure, Private and Confidential Screening and Proactive Healthcare Solutions
✅ Clinician Assisted Specimen Collection at Network Facilities or at On-Demand Location
✅ Convenient Comprehensive Offerings in One Place, Trusted by 350K+ Patients
GENETIC TESTS CATALOG
✨ DNA Methylation Testing to explore epigenetic markers
🌟 Hereditary Cancer and Carrier Screening for familial health risks
🧬 Health Risks Assessment and Customized Wellness Planning
💊 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
⚕️ COLOTECT Colon Cancer Screening for early detection
🩺 Genetic Testing for Diseases and Afflictions to identify predispositions
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:
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.
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.
Confirm the paternity of your unborn baby with a 99.9% accurate test that requires only blood samples from the mother and alleged father
A Paternity DNA Test is used to determine who is the genetic Father of a Child or Children
Non-Invasive Prenatal Testing for detecting fetal chromosomal aneuploidies from maternal blood, such as Down syndrome, Edward syndrome, and Patau syndrome
Carrier screening for Monogenic disease
Thalassemia mutations detection for > 508
Thalassemia mutation including common
Alpha- and Beta-thalassemia
Newborn genetic screening for 112 genetic diseases.
Newborn 48 metabolic disorders screening
Clinical whole exome sequencing for detection and diagnosis of rare diseases
Comprehensive Genetic Panel for Cancer Risk Assessment
Price: 42,500 THB
The SENTIS™ Hereditary Cancer Screening – Male Package is a comprehensive genetic test designed to evaluate inherited cancer risks by analyzing 79 genes associated with 22 types of hereditary cancers. It is ideal for men seeking proactive insights into their long-term health or who have a family history of cancer.
What This Test Covers
Genes Analyzed: 79 genes clinically associated with hereditary cancer syndromes
Cancer Types Included: 22 types, including prostate, colorectal, breast (in men), pancreatic, stomach, and others
Risk Identification: Detects single nucleotide variants (SNVs), insertions/deletions (indels), and copy number variations (CNVs)
Clinical Utility: Helps guide screening, prevention, and treatment strategies based on genetic predisposition
Sample Type: 3 cc of blood (EDTA tube)
Fasting Required: No
Test Duration: Quick 10–20 minute sample collection
Turnaround Time: 26 business days
Report Delivery: Results sent securely via email
Early Risk Detection: Gain clarity on inherited cancer risks before symptoms appear
Personalized Health Management: Use your genetic profile to make informed decisions about monitoring and prevention
Family Insight: Results may provide helpful information for relatives who may share similar genetic risks
No Special Preparation Needed: Simple, fast, and non-fasting blood draw
Individuals with a family history of cancers such as prostate, colorectal, or breast cancer
Those planning for long-term health and cancer prevention
Individuals looking for personalized medical guidance based on genetic risk
Explore Your Ancestry, Optimize Your Health, and Embrace Your Unique Genetic Traits with Our Comprehensive DNA Testing Service
mail@medex.co.th
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.
Unveil Your DNA: Discover the Secrets Within
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.
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.
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.
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.
Frequently Asked Questions
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.
Prenatal genetic testing is a medical examination performed during pregnancy to assess the genetic health and development of the fetus. It aims to identify potential genetic abnormalities, chromosomal disorders, or inherited conditions in the unborn child. Prenatal genetic testing offers valuable information to expectant parents and healthcare providers, aiding in making informed decisions about the pregnancy, including choices about the continuation of the pregnancy, preparing for medical interventions, or planning for the care of a child with special needs.
1. Screening Tests: Prenatal screening tests are typically the first step in assessing the risk of a fetus having a genetic disorder. These tests are non-invasive and include options like non-invasive prenatal testing (NIPT), maternal serum screening (also known as triple or quad screen), and ultrasound examinations. They provide information about the likelihood of the fetus having certain genetic conditions. If a screening test suggests an increased risk, further diagnostic testing may be recommended.
2. Diagnostic Tests: Prenatal diagnostic tests are more invasive and definitive. They are performed when a screening test indicates a higher risk of a genetic disorder or when there are other indications for a diagnostic assessment. Common diagnostic tests include chorionic villus sampling (CVS) and amniocentesis. These tests directly examine the genetic material of the fetus, providing a definitive diagnosis of genetic conditions, chromosomal abnormalities, or other genetic disorders.
Embark on a unique journey of self-discovery with our DNA testing services. Uncover your ancestral origins, gain insights into your health, and explore the fascinating world of your genetic traits. Your DNA holds the key to your past, present, and future, and we're here to help you decode it.
Empower yourself with personalized genetic insights. Our DNA testing service offers a window into your genetic makeup, helping you make informed decisions about your health and lifestyle. It's time to take control of your destiny and embrace the power of your DNA.
Unveil the mysteries of your genetic code with our cutting-edge DNA testing. Gain valuable knowledge about your ancestry, health predispositions, and unique traits. Armed with this information, you can make proactive choices for a healthier and more fulfilling life.
Rating
good service. with attention and care.
I have no words, they saved us
Fast results , polite , clean , fair price
The staff were helpful and the process was smooth . Results and documents were provided as requested. Very professional
Best clinic in Bangkok. I have been there two times and one time they helped me organize a visit in another hospital without any fees! The best! Highly recommended
Fast and efficient clinic, great service from Flor
MedEx was very efficient and they were quick to respond to my messages. The test results were very detailed and well organized in the final report. A doctor video called me and went over all my test results. My experience with MedEx was as good as anything I experienced dealing with many specialists in the USA Thanks!
I sent a query via WhatsApp regarding a ongoing medical issue and needed a quick checkup, They responded instantly to confirm they could help and did so that evening.
They are open day everyday and would recommend for anyone looking for English staff and good customer service.
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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.
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.
For the purposes of this Refund and Return Policy:
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.
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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.
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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:
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.
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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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