Genetic Test: The Key to Personalized, In-Depth Health Care
Our health is not determined by lifestyle habits alone. A deeper factor that plays an important role is our DNA. Genetic Testing is a powerful tool that reveals vital information about disease risks and the body’s potential. It provides insights that go far beyond standard health check-ups, helping you plan health care strategies that truly match your unique body.
What is a Genetic Test?
A Genetic Test is the analysis of DNA — the “blueprint of life” that guides the body’s functions. The information it provides does more than reveal risks of certain diseases. It also identifies which types of food, exercise, and even medications are most suitable for your body.
The results do not mean you will definitely develop an illness. Instead, they serve as an early signal that allows you to plan and take preventive steps with confidence.
Genetic vs. Epigenetic
- Genetic: Fixed information inherited from your parents, unchangeable throughout life.
- Epigenetic: Gene expression that can change depending on environment and lifestyle, such as diet, sleep, and stress.
Even if certain genes increase your risk, living a healthy lifestyle can help reduce it significantly.
Why Consider Genetic Testing?
- Identify the risk of chronic diseases early, including cancer, diabetes, and cardiovascular conditions.
- Tailor nutrition and exercise programs to align with your genetic profile.
- Choose medications that are effective and reduce the risk of side effects.
- Assess biological age and cellular degeneration.
- Develop a clear, long-term health plan.
Genetic Testing at LINNA Clinic
Epigenetic Test
Assesses how your environment and lifestyle choices affect gene expression, with recommendations for restoring balance and improving overall health.
DNA Methylation Test
Analyzes biological age and cellular health by examining DNA methylation patterns. This test helps reveal whether your body is aging faster or slower than your chronological age, and evaluates risks of chronic disease.
Cancer Genetic / Oncogenetic Test
Detects mutations in genes linked to cancer, allowing you to understand risks, create preventive screening plans, and select more precise treatment options if necessary.
Telomere Test
Measures the length of telomeres — protective caps at the ends of chromosomes. Shorter telomeres are associated with accelerated cellular aging and chronic disease. This test is an essential tool for designing personalized anti-aging strategies.
The Testing Process
- Collection of saliva or blood samples
- Analysis in internationally accredited laboratories
- Delivery of comprehensive and easy-to-understand reports
- Consultation with LINNA Clinic specialists to design a personalized health plan
Important Notes Before Testing
- Results indicate risk and tendencies, not a confirmation that you will develop a disease.
- Environmental and lifestyle factors still play a significant role in your health.
- Certain tests, such as Epigenetic and Telomere assessments, should be repeated every 1–2 years to track progress.
Conclusion
Genetic Testing is not only about identifying risks — it opens the door to a new way of managing your health with precision and personalization. ✨
At LINNA Clinic, we integrate genetic insights into comprehensive health strategies — from chronic disease prevention to anti-aging programs and personalized nutrition plans.
With our team of medical experts and internationally certified laboratories, every step of the process is accurate, safe, and designed to create a lasting health plan for your future.
Because good health is the foundation of a confident life,
start today with Genetic Testing at LINNA Clinic.
📍 Book your health consultation today:
Line: @linnaclinic
Tel: +66 63 609 8888
WhatsApp: +66 91 979 9554
Find and Order Laboratory Tests
Anti-Desmoglein 1 (Dsg1) Ab:
2,860 THB
Detects antibodies to desmoglein 1, used to diagnose pemphigus foliaceus, an autoimmune skin disease causing skin blistering.
serum 1-2 ml.
Autoimmune Panel,Skin Disorder Testing
11151
Specific IgE for Gluten(f79):
2,600 THB
Measures specific IgE antibodies to gluten, used to diagnose gluten sensitivity or wheat allergies.
serum 1 ml
Celiac Disease Panel,Food Allergy Testing
11152
FoundationOne Liquid (ACT) (FOUNDATION MEDICINE, INC.):
293,930 THB
Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
Whole blood in FoundationOne Liquid collection tubes (Streck BCT tube X 2) 1. ( Streck tube ) 2. + Request+Consent form Load Salesforce 3.
Cancer Genomic Panel,Liquid Biopsy Testing
11148
Pregnenolone, LC/MS/MS [Questdiagnostic]:
32,220 THB
Measures pregnenolone hormone levels, used to assess adrenal function and hormonal balance.
Serum 2 ml (DO NOT USE GEL TUBES)
Hormonal Panel,Adrenal Function Tests
11149
ANORA Miscarriage testing(BCC):
51,200 THB
Detects chromosomal abnormalities, large deletions or duplications, and uniparental disomy in miscarriage tissue to determine causes of pregnancy loss.
0.5 mm^3 tissue in container with NSS and maternal blood in Special kit **Fresh tissue in NSS and maternal EDTA blood 4-6 ml are alter- native in case of no anora kit** // PBS/NSS NSS BCC 17/11/22
Genetic Miscarriage Panel,Chromosomal Abnormality Testing
11150
FoundationOne HEME (Longitudinal Program case):
214,760 THB
Next-generation sequencing test for hematologic cancers (leukemia, sarcoma), identifying genomic alterations, including base substitutions, insertions, deletions, and rearrangements.
Turnaround Time 1 month
11145
Gene Agnostic Parallel (GTP) (Gene Agnostic):
212,459 THB
Gene-agnostic parallel sequencing test to identify genetic mutations associated with cancer.
1. Blood in streck tube (there are 2 streck tubes) and 2. FFPE tissue in collection kits
Hereditary Cancer Panel,Genetic Screening
11146
Screening for common drug(Urine):
10,238 THB
Screens for common drugs of abuse using liquid chromatography/tandem mass spectrometry (LC-MS/MS), with detection limits varying by substance.
random urine 50 ml (minimum 5 ml)
Toxicology Panel,Drug Abuse Testing
11147
Ethylbenzene (Sum of mandelic acid and phenyl- glyoxylic acid )(HPLC):
1,620 THB
Measures levels of ethylbenzene metabolites (mandelic acid and phenylglyoxylic acid) in urine, used to assess occupational exposure.
Random Urine 10-20 mL (End of Shift)
Occupational Health Panel,Toxicology Testing
11142
JAK2 V617F mutation:
7,088 THB
Detects JAK2 V617F mutation, associated with myeloproliferative disorders like polycythemia vera, using allele-specific PCR (AS-PCR).
EDTA whole blood 3-5 ml or EDTA bone marrow 3-5 ml
Myeloproliferative Disease Panel,JAK2 Testing
11143
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Anti-Desmoglein 1 (Dsg1) Ab:
2,860 THB
Description: Detects antibodies to desmoglein 1, used to diagnose pemphigus foliaceus, an autoimmune skin disease causing skin blistering.
Specimen: serum 1-2 ml.
Related Tests: Autoimmune Panel,Skin Disorder Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Specific IgE for Gluten(f79):
2,600 THB
Description: Measures specific IgE antibodies to gluten, used to diagnose gluten sensitivity or wheat allergies.
Specimen: serum 1 ml
Related Tests: Celiac Disease Panel,Food Allergy Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
FoundationOne Liquid (ACT) (FOUNDATION MEDICINE, INC.):
293,930 THB
Description: Analyzes blood samples from patients with solid tumors (lung, breast, colon, etc.) using next-generation sequencing to detect genomic alterations.
Specimen: Whole blood in FoundationOne Liquid collection tubes (Streck BCT tube X 2) 1. ( Streck tube ) 2. + Request+Consent form Load Salesforce 3.
Related Tests: Cancer Genomic Panel,Liquid Biopsy Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Pregnenolone, LC/MS/MS [Questdiagnostic]:
32,220 THB
Description: Measures pregnenolone hormone levels, used to assess adrenal function and hormonal balance.
Specimen: Serum 2 ml (DO NOT USE GEL TUBES)
Related Tests: Hormonal Panel,Adrenal Function Tests
Add to WishlistRemove from Wishlist
Add to Wishlist
ANORA Miscarriage testing(BCC):
51,200 THB
Description: Detects chromosomal abnormalities, large deletions or duplications, and uniparental disomy in miscarriage tissue to determine causes of pregnancy loss.
Specimen: 0.5 mm^3 tissue in container with NSS and maternal blood in Special kit **Fresh tissue in NSS and maternal EDTA blood 4-6 ml are alter- native in case of no anora kit** // PBS/NSS NSS BCC 17/11/22
Related Tests: Genetic Miscarriage Panel,Chromosomal Abnormality Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
FoundationOne HEME (Longitudinal Program case):
214,760 THB
Description: Next-generation sequencing test for hematologic cancers (leukemia, sarcoma), identifying genomic alterations, including base substitutions, insertions, deletions, and rearrangements.
Specimen: Turnaround Time 1 month
Add to WishlistRemove from Wishlist
Add to Wishlist
Gene Agnostic Parallel (GTP) (Gene Agnostic):
212,459 THB
Description: Gene-agnostic parallel sequencing test to identify genetic mutations associated with cancer.
Specimen: 1. Blood in streck tube (there are 2 streck tubes) and 2. FFPE tissue in collection kits
Related Tests: Hereditary Cancer Panel,Genetic Screening
Add to WishlistRemove from Wishlist
Add to Wishlist
Screening for common drug(Urine):
10,238 THB
Description: Screens for common drugs of abuse using liquid chromatography/tandem mass spectrometry (LC-MS/MS), with detection limits varying by substance.
Specimen: random urine 50 ml (minimum 5 ml)
Related Tests: Toxicology Panel,Drug Abuse Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
Ethylbenzene (Sum of mandelic acid and phenyl- glyoxylic acid )(HPLC):
1,620 THB
Description: Measures levels of ethylbenzene metabolites (mandelic acid and phenylglyoxylic acid) in urine, used to assess occupational exposure.
Specimen: Random Urine 10-20 mL (End of Shift)
Related Tests: Occupational Health Panel,Toxicology Testing
Add to WishlistRemove from Wishlist
Add to Wishlist
JAK2 V617F mutation:
7,088 THB
Description: Detects JAK2 V617F mutation, associated with myeloproliferative disorders like polycythemia vera, using allele-specific PCR (AS-PCR).
Specimen: EDTA whole blood 3-5 ml or EDTA bone marrow 3-5 ml
Related Tests: Myeloproliferative Disease Panel,JAK2 Testing
Add to WishlistRemove from Wishlist
Add to Wishlist