Experience MedEx Seamless Care Delivery — 10% OFF on Your First Appointment - Use 'TRYMEDEX' Coupon Code on Checkout //////////////////////////////////// General Price List — Consultation: 750 THB | Home Lab Test Service Fee: 750 THB (FREE for Orders Over 5,000 THB)
From preventive cancer screening to fertility planning, biological age, pharmacogenomics and 700+ trait reports — MedEx offers the broadest genetic testing catalog in Thailand. Walk in to Sukhumvit 13, or have a kit delivered anywhere in the world.
Pick the closest one — it filters the catalog for you. Or answer three questions instead.
Genetic testing has come a long way from "spit in a tube and learn your ancestry." Here's how MedEx's catalog is structured — pick the category that matches what you're trying to find out.
Find out if you carry inherited mutations (BRCA1/2, Lynch syndrome and 75+ other genes) that raise your risk of breast, colon, prostate, ovarian and other cancers.
Make confident decisions before, during, and after pregnancy. Carrier screening for both parents, non-invasive prenatal tests, and newborn metabolic screens.
500+ to 700+ reports covering nutrition, fitness, skin, sleep, behavior, and 50+ trait insights. Lifestyle DNA for biohackers, athletes, and the curious.
For undiagnosed conditions, suspected genetic disorders, or unexplained symptoms — clinical-grade exome sequencing reveals what standard tests miss.
Confidential paternity testing — including non-invasive prenatal options that need only a maternal blood sample. Legal-grade or peace-of-mind formats available.
The 2026 frontier: epigenetic clocks tell you how old your cells actually are. Methylation testing reveals how your lifestyle, diet, and stress are aging you.
Five years ago, most genetic tests were either ancestry kits or expensive hospital-only diagnostics. 2026 is different. Whole-genome sequencing is now routine. Epigenetic clocks can tell you your real biological age. Pharmacogenomic tests change how doctors prescribe psychiatric and cardiovascular drugs. And hereditary cancer panels — once reserved for high-risk families — are now affordable enough to be a baseline preventive screen.
What changed? Three things. Sequencing costs collapsed. AI-powered interpretation finally turned raw genetic data into actionable reports a non-specialist can read. And clinicians caught up: hereditary cancer screening, pre-natal NIPT, and pharmacogenomics are now firmly in standard preventive care globally.
MedEx is Thailand's most complete genetic testing partner — combining laboratory-grade tests from internationally accredited partner laboratories with English-language reports, geneticist consultations, and worldwide kit delivery. Whether you want a single methylation snapshot or 700 trait reports, walk in to Sukhumvit 13 or order a kit anywhere in the world.
The twelve tests our patients book most often. Every one includes an English report, optional geneticist consultation and secure result delivery. See all 67 tests →
This is a shortlist. Browse the full menu of 67 tests or talk to our team — prices, turnaround times and availability are confirmed at booking. Clinician-assisted collection at your home or hotel is available in Bangkok and 30+ provinces for an additional 750 THB. Screening tests are not diagnostic; results should be interpreted by a clinician alongside your clinical and family history.
One cheek swab, and more than five hundred reports on how your body actually works — what to eat, how to train, which medications suit you, what you may carry silently, and where your ancestry begins. Suitable for every age, from one month old upwards, and it only needs to be done once.
Includes full methylation analysis of MTHFR, COMT, MTR, MTRR and BHMT. Oral swab — no blood, no fasting, no preparation. Results delivered with written interpretation by email and in the MedEx app. Kits ship worldwide.
Oral swab only — no blood, no fasting, no preparation. Kits ship worldwide with prepaid return.
An actual Premium 500+ report with the patient details removed. Page through it below — nothing here is a mock-up.
Tap any group to see every condition, nutrient, drug or trait it reports on. This is the complete list — nothing is held back.
Not sure whether this or a clinical panel is right for you? A genetic counsellor will tell you honestly, at no charge — including when the answer is "you don't need this test".
Genetic testing isn't just for people with rare diseases or strong family histories. Here are the most common reasons our patients walk in.
If close relatives had breast, ovarian, prostate, colon, pancreatic, or stomach cancer — especially before age 50.
→ SENTIS Hereditary Cancer PanelBoth partners-to-be can find out if they're silent carriers of inherited conditions before conception.
→ VISTA Carrier ScreeningWant safe, non-invasive testing of fetal genetic health. From 10 weeks, no risk to baby.
→ NIFTY NIPTAntidepressants, ADHD meds, or pain meds that didn't work or caused side effects — pharmacogenomics explains why.
→ Pharmacogenomics PanelWant to know your inherited disease risks before symptoms appear, so you can intervene early.
→ DNALL Prestige (700+ reports)Athletes, biohackers, and execs who want to know their genetic limits and optimal strategies.
→ DNA Story Premium (best seller)Track how your lifestyle is biochemically affecting how fast your DNA actually ages.
→ Epigenetic Age + TelomerePersistent symptoms that mainstream tests can't explain. Whole exome sequencing finds the genetic cause.
→ Whole Exome SequencingFrom the most common chromosomal screens to comprehensive analyses including mosaic trisomies and miscarriage-risk markers. All non-invasive, all from 10 weeks of pregnancy, all from a single maternal blood draw with no miscarriage risk.
Chromosome-count screening for single or twin, natural or IVF pregnancies. The 10-chromosome tier adds mosaic trisomies 8, 9 and 16.
10,000 – 15,000 THB · 3–7 daysScreens chromosomes 1–22 plus deletion and duplication syndromes and sex chromosome aneuploidies including Turner syndrome. Singleton and twin, 10–24 weeks.
19,000 – 30,000 THB · 5–7 daysThe only method here that separates fetal from maternal DNA, enabling zygosity and triploidy assessment. The Extended tier adds five microdeletion syndromes.
17,999 – 29,999 THB · donor & twin validatedOver 99.9999% accuracy, handled with full confidentiality. Choose peace-of-mind testing or a full legal chain of custody — the science is identical, the paperwork is not.
Analyses fetal DNA circulating naturally in the mother's bloodstream. No amniocentesis, no CVS, no needle near the baby, and no miscarriage risk.
Available as private peace-of-mind testing or with a full documented chain of custody, making the result admissible for court, immigration and birth registration.
Establishes family relationships indirectly: siblingship confirms shared parentage, grandparentage verifies a child's link to grandparents, and avuncular testing checks a biological connection to an uncle or aunt.
Accredited to ISO/IEC 17025:2017 by the Bureau of Laboratory Quality Standards (BLQS), Department of Medical Sciences, Ministry of Public Health. Chain-of-custody collection is documented at every step, which is what makes a result legally defensible rather than merely accurate.
Sixty seconds, no email required. We'll point you at the right panel — and tell you honestly when the answer is "speak to a counsellor first".
Most genetic tests need only a swab or a small blood sample. Kits ship worldwide. Reports are emailed in English.
Submit the form below, message us on WhatsApp, or walk in to MedEx Neo Sukhumvit 13. Our team confirms your test choice and pricing.
Most tests need a swab — we deliver kits worldwide. Blood-based tests done at our clinic or by a nurse at your home (750 THB).
Some tests run locally; many are sent to internationally accredited specialist laboratories. Strict chain of custody throughout.
Illustrative reports emailed in English. Geneticists and specialists available for interpretation and lifestyle recommendations.
Choose the collection method that suits you. Most genetic tests need only a swab — kits ship worldwide. Blood-based tests are done at our clinic or via nurse home visit.
Visit MedEx Neo Sukhumvit 13 (or Phra Khanong, Chiang Mai) at your convenience. No appointment needed.
Registered nurse to your home, hotel, or office anywhere in Bangkok or 30+ Thai provinces.
Most genetic tests use a swab — we ship the kit, you collect at home, ship it back with prepaid shipping.
Browse the catalog and click "Book" on any test. Our team confirms availability and price.
Choose clinic, home visit or kit by post. Pay securely by card, bank transfer or PromptPay.
Our team contacts you within minutes to schedule. Walk-in? Just stop by. Home visit? We dispatch a nurse. Kit? It ships.
Reports emailed in English with international ranges. Geneticist consult included for clinically significant findings.
Prefer to talk first? Call +66-02-544-0001 · WhatsApp our team · Email [email protected]
It depends on the test. NIPT and paternity are the fastest at 5–7 days. Postnatal paternity can be 3–5. Hereditary cancer panels and carrier screening run 21–26 business days. Whole exome sequencing is 15 days for Xome Express and 40 for Clinical WES. The large lifestyle panels take 30–45 days because of the volume of reports generated. We confirm exact timing when you book.
For DNA testing, no — your genes don't change based on what you ate. Most tests use a cheek swab or a blood draw with no fasting. The exceptions are COLOTECT, which has simple stool collection instructions, and NOVA metabolic screening, which is timed to days 3–7 after birth. We send test-specific preparation instructions when you book.
For most tests, yes. Anything using a swab or saliva can be done anywhere — we ship a self-collection kit with instructions and prepaid return shipping.
Blood-based tests need a draw. You can either book during a trip to Thailand, or we can help arrange phlebotomy at a partner lab in your country for an additional fee. Some prenatal and clinical tests carry country-level regulatory restrictions, so check with our team first.
Often, when the test is ordered for a diagnostic reason. Hereditary cancer screening, carrier screening and prenatal NIPT are the most commonly reimbursed. Wellness and longevity panels are almost always self-pay.
We issue itemised invoices for reimbursement claims. Send us your policy details before booking and we'll tell you what we've seen from that insurer.
Screening tells you your risk. Diagnosis tells you what you have. NIPT, carrier screening and hereditary cancer panels are screening tests — a high-risk result means further testing is needed, not that a condition is confirmed.
Diagnostic tests such as amniocentesis, chorionic villus sampling and whole exome sequencing examine the genetic material directly and give a definitive answer. A high-risk screening result is the trigger for a diagnostic test, never a conclusion on its own.
You won't be left to work it out from a PDF. Every clinically significant finding triggers a genetic counsellor consultation covering what the result means, what it doesn't mean, and what to do next.
For cancer-risk findings such as BRCA or Lynch syndrome, we coordinate referrals to oncology specialists across our network of JCI-accredited Thai hospitals. Most people find that knowing early is what makes prevention possible.
Yes. MedEx operates under Thailand's PDPA. Your data is encrypted in transit and at rest, released only to you and clinicians you authorise, and never shared with insurers or employers. Paternity and legal testing additionally follows a documented chain of custody.
Anyone with a first- or second-degree relative diagnosed with breast, ovarian, prostate, colorectal, pancreatic or gastric cancer — particularly if the diagnosis came before age 50, if several relatives are affected, or if one relative had more than one primary cancer.
It's also reasonable if you simply want a baseline for long-term health planning. A negative result is genuinely reassuring; a positive one changes your screening schedule, not your prognosis.
From 10 weeks of pregnancy, once fetal fraction in maternal blood typically exceeds 4%. Detection is around 99% for Down syndrome, 97.4% for Edwards syndrome and 87.5% for Patau syndrome. Sex chromosome detection is about 95% accurate.
Testing earlier than 10 weeks, maternal obesity, or a vanishing twin can all lower fetal fraction and produce an inconclusive result.
Not the accuracy — the paperwork. A peace-of-mind test and a legal test use identical science and give identical numbers. What makes a result admissible in court, for immigration or for birth registration is the documented chain of custody: verified identity, witnessed collection and a tracked sample.
Bring parent ID or passports and the child's birth certificate. If the child is under 20, the mother must attend.
Trio, if the parents are available. Sequencing the child alongside both biological parents lets the lab identify de novo mutations and confirm inheritance patterns, which raises the diagnostic yield by up to 30% over testing the child alone.
Proband-only WES is the right choice when parents are unavailable, or as a faster first pass via Xome Express at 15 business days.
Yes, with parental consent, and the right test depends on age. NOVA metabolic screening is timed to days 3–7 after birth. NOVA genetic screening covers newborn to five years. Rare disease panels and WES have no age limit and are usually ordered when a child has symptoms without a diagnosis.
Adult-onset predictive testing in healthy children is generally discouraged, and our counsellors will talk that through with you rather than simply processing the order.
Still have a question? Message our team on WhatsApp or call +66-02-544-0001, 24 hours.
From BTS Nana
Walking · ~5 mins
From BTS Asok
Walking · ~7 mins
From MRT Sukhumvit
Walking · ~8 mins
From BTS Phra Khanong
Walking · ~3 mins
From BTS Saphan Taksin
Taxi / Grab · ~10 mins
From Bus Terminal 3
Taxi / Songthaew · ~5 mins
Our expert medical team is ready to guide you. Choose your preferred channel and connect with us instantly — we're here to help.
Rating
My experience here at the medex clinic was excellent. The staffs are really professional and kind. Doctors here are really knowledgeable and skilled they took time to listen to all of my concerns. I felt really comfortable throughout the entire process. I highly highly recommend this clinic.
I’ve been here more than 3 times already. I did DNA testing, blood tests, and other checkups here. The staff is always kind, professional, and very helpful. They speak good English, which makes everything much easier for foreigners. Highly recommended.
Staff were super sweet and nice. Very helpful and supportive. All questions answered. The clinic was very clean and tidy. I felt like I was in safe hands.
Best place for the medical checkups and diagnostic with very friendly staffs who will guide you with professional care. My experience with MedEx was great and I totally recommend paying them a visit.
The clinic is excellent. Very clean, fast service, everyone answered questions well. The place is clean and the service is great. My boyfriend really liked it. We will definitely go again next time. ⭐⭐⭐⭐⭐⭐⭐
Excellent service and care
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MedEx is a one-stop digital care navigation concierge backed by physical infrastructure, owning the patient experience and decentralizing the care continuum across Asia—integrating provider aggregation, satellite clinics, telemedicine, and at-home care.
MedEx is a one-stop digital care navigation concierge backed by physical infrastructure, owning the patient experience and decentralizing the care continuum across Asia—integrating provider aggregation, satellite clinics, telemedicine, and at-home care.
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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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To exercise Your right of cancellation, You must notify Us in writing. You can inform us of your decision by:
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