Genetic & Gene Analysis: The Key to Personalized Health
In every cell of the human body, our genes act like an instruction manual. They influence how we metabolize nutrients, respond to the environment, and our likelihood of developing certain conditions.
Understanding your genetics is a crucial step in preventive medicine—enabling health care that is precise, personalized, and sustainable
Why Do Genetics Matter for Your Health?
Your genetic code is inherited, while each gene controls specific functions—such as nutrient utilization, drug response, or energy regulation. Even small differences in genes can make people’s health needs noticeably different.
Examples include:
- Genes affecting absorption of vitamins such as vitamin D, vitamin B12, and iron
- Genes influencing responses to caffeine and alcohol
- Inherited variants that raise the risk of heart disease or diabetes
- Genes involved in fat metabolism and energy balance, impacting weight management
What Is the Genetics & Gene Testing Program?
Our Gene Insights Program integrates DNA testing with clinical assessment to create a personalized plan for nutrition and health.
It includes:
- Genome Analysis: Variants related to nutrition and health
- Blood Longevity Panel: Nutrient levels, inflammation markers, and metabolic indicators
- Body Composition Analysis: Muscle mass, visceral fat, and cardiovascular risk
- Consultation with Specialists: Clear interpretation and practical guidance
- Personalized Action Plan: Tailored recommendations for diet, supplements, and lifestyle aligned with your genetics
Who Is This Program For?
Genetic testing isn’t only for people who are ill—it suits anyone who wants a deeper understanding of their body, including those who:
Want to prevent disease before symptoms appear
Wish to learn which foods are compatible with their genetics
Are interested in personalized nutrition
Seek proactive, long-term health strategies
Benefits of Genetic & Gene Testing
Precision
Genetic insights help clinicians analyze health needs more deeply than general guidelines.
Prevention
Identify inherited risks and reduce the chance of future disease.
Confidence
Receive a health plan tailored to your genetic profile.
Genetics, Genes & Nutrition
Genes influence how your body uses and manages nutrients, so people vary in tolerance and sensitivity to different foods. For example:
Lactose digestion genes: Some people drink milk comfortably; others experience bloating.
Caffeine response genes: Some feel energized; others develop palpitations.
Fat storage–related genetics: Linked to risks of obesity and diabetes.
Summary
Genetics opens a new dimension in understanding health. Genetic testing turns care from reactive treatment into smart, precise life planning.
If you want care that is truly personal, practical, and sustainable, genetic and gene testing is a powerful option to consider.
BDMS SPOT-MAS PACKAGE – Genetic Screening for 10 Types of Cancer
Special price ฿16,900
With SPOT-MAS technology, multi-cancer screening is made possible through just a single blood test. This allows you to monitor your health and cancer risks with peace of mind, and provides an excellent option as part of your annual proactive health check.
- This programme is available from 1 October 2025 to 15 November 2025.
- The price includes the doctor’s interpretation fee and hospital service charges, but excludes any additional expenses that may arise from further diagnostic examinations or treatments if abnormalities are detected.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
Conditions for Undergoing the Test
✅ Who should undergo the test
Recommended for individuals who meet any of the following:
- Age 40 years or older, even without cancer symptoms or history.
- Family history of major cancers or multiple affected relatives.
- Current or past heavy smoking or regular alcohol use. Occupational or environmental exposure to carcinogens (e.g., heavy metals, industrial chemicals).
- Individuals seeking proactive multi-cancer screening with one blood test.
❌ Who should not undergo the test
Testing is generally NOT recommended if any of the following apply:
- Individuals younger than 18 years.
- Pregnant women.
- Currently under treatment for active or metastatic cancer.
- Recent bone marrow transplantation or blood transfusion within the past 6 months.
- Severe hematological disorders or other conditions that could interfere with circulating DNA analysis.
Notes
- SPOT-MAS is a screening tool, not a diagnostic test.
- Any positive signal requires confirmatory diagnostic testing (e.g., imaging, biopsy).
- Pre- and post-test counseling by a qualified clinician or genetic specialist is recommended.
- Recommended frequency: Annually (yearly screening).
What is this screening?
- Liver and bile duct cancer
- Lung cancer
- Breast cancer
- Colorectal cancer (colon and rectum)
- Gastric cancer
- Pancreatic cancer
- Ovarian cancer
- Oesophageal cancer
- Endometrial cancer
- Head and neck cancer
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445-7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- A blood sample will then be collected without the need for fasting or dietary restrictions.
- The sample will be analysed in the laboratory, with results available in approximately 30 days.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
Hereditary Cancer Gene Panel
Special price ฿26,320 ฿25,000
The Hereditary Cancer Gene Panel is an in-depth genetic test designed to identify inherited cancer risks that may have been silently passed down within your family. It helps you to understand your personal risk, enabling you to plan preventative measures and manage your health in the most precise and effective way – before the disease develops.
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges, but excludes any additional expenses that may arise from further diagnostic examinations or treatments if abnormalities are detected.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
- Please review the terms and conditions before purchasing the package.
Conditions for Undergoing the Test
✅ Who should undergo the test
You should consider testing if ANY of the following apply:
1. Personal cancer history
- Diagnosed with breast, ovarian, fallopian tube, peritoneal, colorectal, endometrial, pancreatic, or prostate cancer before age 50.
- Multiple primary cancers in one person.
- Rare cancers such as male breast cancer.
2. Family history
- First-degree relative (parent, sibling, child) with any of these cancers, especially diagnosed before age 50.
- Two or more relatives with the same or related cancers (e.g., breast–ovarian, colon–endometrial).
- One relative with multiple primary cancers.
3. Known familial gene mutation
- A family member has a known pathogenic mutation such as BRCA1/2 or Lynch syndrome genes (MLH1, MSH2, MSH6, PMS2, EPCAM).
4. High-risk ancestry
- Belong to an ancestry with higher prevalence of hereditary cancer genes, such as Ashkenazi Jewish or other high-risk populations.
❌ Who should not undergo the test
Testing is generally NOT recommended if all of the following apply:
- No personal history of related cancers and no first or second-degree relatives with these cancers.
- Only one family member with cancer diagnosed after age 60.
- No known cancer-related gene mutation in the family.
Note
- Pre and post-test genetic counseling is strongly recommended.
- Individuals not meeting criteria should follow routine age and risk-based cancer screening (e.g., mammogram, colonoscopy).
- Recommended frequency: once in a lifetime.
What is this screening?
This is a screening test for genes associated with hereditary cancers, which account for around 5–10% of all cancer cases. Knowing whether you carry genetic mutations that increase your risk can be a key factor in planning early surveillance and preventative measures.
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445–7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- A blood sample will then be collected without the need for fasting or dietary restrictions.
- The sample will be analysed in the laboratory, with results available in approximately 21 days.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
Colorectal Cancer Gene Stool Test
Special price Original price was: ฿26,320.฿12,000
This is a Stool DNA Test, which analyses the DNA of cancer cells from a stool sample. It is a convenient and highly accurate method that enables the detection of risks at an early stage. The test is suitable for annual screening or as an alternative to colonoscopy at regular intervals.
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges, but excludes any additional expenses that may arise from further diagnostic examinations or treatments if abnormalities are detected.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
- Please review the terms and conditions before purchasing the package.
Conditions for Undergoing the Test
✅ Who should undergo the test
Stool DNA testing is recommended for adults who:
- Are 45 years or older
- Have average risk for colorectal cancer (no high-risk hereditary syndrome).
- Have no current symptoms suggesting colorectal cancer (e.g., rectal bleeding, unexplained iron-deficiency anemia, significant unexplained weight loss).
- Are able and willing to undergo a colonoscopy if the stool DNA test is positive.
- Prefer a non-invasive screening method between colonoscopies.
❌ Who should not undergo the test
Stool DNA testing is not recommended for individuals who:
- Have a personal history of colorectal cancer, advanced adenomas, or high-risk polyps.
- Have inflammatory bowel disease (ulcerative colitis or Crohn’s disease involving the colon).
- Have a strong family history or known inherited colorectal cancer syndrome (e.g., Lynch syndrome, familial adenomatous polyposis).
- Currently have symptoms suggestive of colorectal cancer such as rectal bleeding, unexplained anemia, persistent abdominal pain, or significant weight loss.
- Had a positive stool DNA test
- Are unable or unwilling to undergo follow-up colonoscopy if the test result is positive.
Notes
- Stool DNA testing is a test that looks for abnormal DNA from colon cancer or polyps.
- Recommended for average-risk adults ≥45 years old.
- Follow-up: A positive stool DNA test MUST be followed by a diagnostic colonoscopy.
What is this screening?
- This test detects genetic alterations characteristic of colorectal cancer cells (SDC2 Methylation). It is an innovative and effective screening method that helps reduce the anxiety associated with colonoscopy.
Service Procedure
- Please make an appointment at least one day in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2753, 3330 during the hours of 13:00–15:00 only.
- Once your request has been received, the Digestive Care Centre will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Digestive Care Centre, 3rd Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- Collect a fresh stool sample according to the instructions provided and submit it to the laboratory.
- The analysis will take approximately 7 days.
- You will then meet your doctor to review the screening report, which indicates potential risk signals, and to receive advice that will support further diagnostic planning.
Inherited Cardiovascular Gene Panel
Special price ฿34,320 ฿32,000
This is a test that analyses gene groups associated with hereditary heart disease and high blood cholesterol.
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
- Please review the terms and conditions before purchasing the package.
Conditions for Undergoing the Test
✅ Who should undergo the test
Recommended if ANY of the following apply:
1.Personal history of cardiac disease
- Cardiomyopathy (hypertrophic, dilated, restrictive)
- Primary arrhythmia syndromes (long QT, Brugada, catecholaminergic polymorphic VT, etc.)
- Unexplained sudden cardiac arrest or recurrent syncope of suspected genetic origin
- Familial Hypercholesterolemia suspicion – LDL-C ≥190 mg/dL in adults (≥160 mg/dL in children) plus family history of premature coronary disease or xanthomas
***AND one or more of the following:
• First-degree relative with premature coronary artery disease (men <55, women <65)
• First-degree relative with LDL-C above these cutoffs
• Presence of tendon xanthomas or corneal arcus before age 45
2.Strong family history of heart disease or sudden death
- One or more first-degree relatives with cardiomyopathy, arrhythmia, or sudden unexplained death (especially <50 years)
- Multiple relatives across generations with similar cardiac conditions
3.Unexplained structural or conduction abnormalities
- Early-onset AV block, unexplained cardiomegaly, or other congenital structural heart disease with suspected genetic cause.
4.Positive or suspicious family gene test
- Known pathogenic or likely pathogenic variant in a cardiac gene (e.g., MYH7, LMNA, SCN5A).
5.Pre-conception or prenatal planning in high-risk families
- Couple with a family history of inherited cardiomyopathy/arrhythmia seeking risk assessment.
❌ Who should not undergo the test
Testing is generally NOT recommended if:
1. No personal or family history suggesting genetic heart disease
- Example: isolated lifestyle-related hypertension or coronary artery disease at older age.
2. Active, advanced heart failure of clearly non-genetic cause
- Example: ischemic heart disease after long-standing atherosclerosis without suggestive family pattern.
3. Recent major blood transfusion or bone marrow transplantation
- May interfere with DNA analysis.
Note
- Pre- and post-test genetic counseling is essential
- Results must be interpreted with clinical correlation
- Negative test does not rule out all genetic causes
- Recommended frequency: once in a lifetime.
What is this screening?
This test provides a comprehensive analysis of gene groups associated with hereditary cardiovascular diseases, focusing on four major conditions:
- Familial hypercholesterolemia: Genetic high blood cholesterol
- Arrhythmia: Severe abnormal heart rhythms
- Cardiomyopathy: Abnormalities of the heart muscle
- Aortopathy: Disorders of the aorta
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445–7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- A blood sample will then be collected without the need for fasting or dietary restrictions.
- The sample will be analysed in the laboratory, with results available in approximately 2 months.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
CardioMed Pharmacogenomic Panel
Special price ฿18,920 ฿15,900
It is a genetic test designed to personalise cardiovascular treatment, helping to determine which medications are most effective for your body and which may pose a higher risk of adverse reactions.
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
What is this screening?
It is a pharmacogenetic (PGx) test that analyses the relationship between your genetic makeup and your body’s response to medications, enabling the optimisation of drug therapy for each individual.
Pharmacogenetic Testing for Cardiovascular Disease
Genetic testing for cardiovascular-related drugs helps identify how your body metabolises and responds to specific medications — allowing doctors to tailor treatments for greater safety and effectiveness.
Cardiovascular drugs
Clopidogrel (CYP2C19)
Anti-arrhythmic and anti-hypertensive drugs
Flecainide, Propafenone (CYP2D6)
Anticoagulants
Warfarin (CYP2C9, VKORC1, CYP4F2)
Lipid-lowering agents
Atorvastatin, Rosuvastatin, Simvastatin (SLCO1B1, CYP2C9, ABCG2)
Comprehensive Pharmacogenetic Testing for Drug Hypersensitivity
Pharmacogenetics for HLA-B Genotyping with HLA-A*31:01
This genetic test identifies HLA-B and HLA-A gene variants associated with severe adverse drug reactions, enabling safer and more personalised medication use.
Anti-gout medication
Allopurinol (HLA-B*58:01)
Anticonvulsant medications
Carbamazepine, Oxcarbazepine (HLA-B15:02, HLA-A31:01, B75 serotype)
Phenytoin, Fosphenytoin (HLA-B*15:02)
Lamotrigine (HLA-B*15:02)
Important Information
- Recommended frequency: once in a lifetime.
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445–7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- Fasting is not required, and you should inform your doctor of all medications you are currently taking.
- The sample will be analysed in the laboratory, with results available in approximately 16 days.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
NutriGene Basic Panel
Special price ฿11,520 ฿10,000
This test analyses fundamental genes related to nutrition to help you understand how your body responds to nutrients, vitamins, and minerals. It creates a personalised nutrition guide based on your genetic information.
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
What is this screening?
This test analyses key genes related to nutrigenomics to understand how your body responds to nutrients, vitamins, and minerals. It serves as a personalised nutrition guide built from your own genetic data. The analysis also covers your metabolic potential, tendency to accumulate fat, response to different types of exercise, and genetic predisposition to non-communicable diseases (NCDs).
It provides insights into:
- How your body responds to major nutrients (carbohydrates, fats, and proteins) and your genetic risk for NCDs such as diabetes, hyperlipidaemia, and hypertension
- Your specific requirements for essential vitamins and minerals
- Your sensitivity to certain food components such as lactose, caffeine, and alcohol
Who is this package suitable for?
- Individuals who are beginning to focus on their health and want to plan a diet that suits their body
- Those who wish to understand their specific requirements for vitamins, minerals, or other nutrients
- Individuals looking to adjust their nutrition for long-term health, using science-based information
Important Information
- Recommended frequency: once in a lifetime.
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445–7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- Please fast for at least 8 hours before the blood draw (water is allowed).
- The sample will be analysed in the laboratory, with results available in approximately 45 days.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
NutriGene Advanced Panel
Special price ฿35,560 ฿27,000
This is an advanced and comprehensive genetic test that provides in-depth insights – not only into your response to nutrients, but also your metabolic potential, tendencies for fat accumulation, response to different types of exercise, and genetic risks for non-communicable diseases (NCDs).
- This programme is available from 1 October 2025 to 31 December 2025.
- The price includes the doctor’s interpretation fee and hospital service charges.
- The hospital reserves the right to amend the programme price as appropriate without prior notice.
What is this screening?
- This is an advanced and comprehensive genetic test that provides in-depth insights—not only into your response to nutrients, but also your metabolic potential, tendencies for fat accumulation, response to different types of exercise, and genetic risks for non-communicable diseases (NCDs).
Who is this package suitable for?
- Individuals seeking a complete, holistic health plan
- Those who want to manage their weight effectively and understand the underlying factors of their metabolism
- People who exercise regularly and want to maximise their physical potential
- Those looking to prevent metabolic-related conditions, such as diabetes and high blood cholesterol
Important Information
- Recommended frequency: once in a lifetime.
Service Procedure
- Please make an appointment at least two days in advance via Line @BNHhospital, by email at [email protected], or by calling 02-0220700 ext. 2847, 4445–7 during the hours of 13:00–15:00 only.
- Once your request has been received, the Health Check-up Department will contact you between 13:00–15:00 or by email to confirm your appointment.
- If you need to reschedule, kindly inform us at least two days in advance, again during 13:00–15:00 only.
- The screening service is provided at the Advanced Diagnostic Centre, 4th Floor, Zone A, BNH Hospital. On the day of your visit, our staff will first provide information about the test.
- Please fast for at least 8 hours prior to the blood draw (water is allowed).
- The sample will be analysed in the laboratory, with results available in approximately 45 days.
- You will meet with a doctor to review the screening report, which will indicate any potential risk signals for various cancers and guide the planning of further diagnostic examinations
- In cases where a positive result is found, a specialist will provide additional consultation and recommend specific diagnostic procedures.
