Diagnostic options · UAE
Molecular Diagnostics tests in Dubai & UAE
Compare available Molecular Diagnostics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.
Tests in this category
781
Listed price range
550.00–150,000.00 AED
Clinical preparation
Confirm test-specific instructions with your clinician or laboratory.
Compare available tests
Molecular Diagnostics test prices
Showing 151–165 of 781 matching tests.
| Test and description | Specimen | Typical duration | Price | Options |
|---|---|---|---|---|
|
TEST-5300
CHRNA1 Gene Slow‑Channel Congenital Myasthenic Syndrome Genetic Test
This genetic test identifies pathogenic variants in the CHRNA1 gene associated with slow-channel congenital myasthenic syndrome. |
Whole Blood, Buccal Swab, or FTA Card | 3–4 Weeks | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-2294
Chromosome 11p15 Silver‑Russell Syndrome Genetic Test
This test evaluates the chromosome 11p15 region for methylation defects, copy number variations, and uniparental disomy associated with Silver-Russell syndrome. |
Whole blood, extracted DNA, or dried blood spot (FTA card) | 3–4 weeks from sample receipt | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-2184
Chromosome 7q11.23 Williams-Beuren Syndrome Genetic Test
This diagnostic test evaluates for microdeletions on chromosome 7q11.23, which are characteristic of Williams-Beuren syndrome. |
Whole Blood, Dried Blood Spot (FTA card), or Extracted DNA | 3–4 Weeks | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-656
Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 1 Test
This test identifies key genetic mutations and deletions associated with Chronic Lymphocytic Leukemia (CLL). It provides crucial information for risk stratification and treatment p... |
Whole Blood (EDTA Tube) | 5 Days (Sample Mon, Report Sat) | 750.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-650
Chronic Lymphocytic Leukemia (CLL) Mutations Detection Panel 2 Test
This test detects key genetic mutations and copy number variations in CLL-associated genes to guide treatment and risk stratification. |
Peripheral Whole Blood (EDTA tube, lavender-top) | 6–7 Days (Sample Mon, Report Sat) | 750.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-654
Chronic Lymphocytic Leukemia (CLL) Prognostic Panel Test
This test evaluates key genetic and immunophenotypic markers in blood or bone marrow to assess the prognosis and guide treatment for Chronic Lymphocytic Leukemia (CLL). |
Whole Blood (EDTA) / Bone Marrow (Heparin) | 7 Business Days | 3,000.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-1718
Chronic Neutrophilic Leukemia (CNL) CSF3R & SETBP Mutation Analysis Test
This test identifies specific activating mutations in the CSF3R and SETBP1 genes, which are key diagnostic markers for Chronic Neutrophilic Leukemia (CNL). |
Bone marrow aspirate or peripheral blood | 7–8 business days | 1,600.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-1712
cKIT Mutation Screening (Exons 9, 11, 13, 17) Test
This test identifies activating or resistance mutations in the KIT gene within specific exons relevant to GIST. |
Tumor Tissue (FFPE block or biopsy slide) | 7–8 days | 1,600.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-5375
CLCN1 Gene Myotonia Congenita Genetic Test
This genetic test evaluates the CLCN1 gene for mutations causing myotonia congenita, a rare inherited muscle stiffness disorder. |
Peripheral Whole Blood or Extracted DNA | 3–4 Weeks | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-1035
Clinical Exome Sequencing (NGS) Test
This test analyzes the coding regions of over 9,300 genes to identify genetic variants associated with rare and undiagnosed diseases. |
Peripheral whole blood (EDTA tube) | 4 weeks | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-467
Clinical Exome Sequencing for Couples (Preconception Carrier Screening) Test
This test analyzes the coding regions of over 20,000 genes in both partners to identify carrier status for autosomal recessive and X-linked disorders. |
Peripheral whole blood (2× 8.5 mL EDTA tubes) or buccal swab per partner | 14 business days | 5,000.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-451
Clinical Exome Trio Sequencing Test
This test identifies genetic variants in the coding regions of genes from a child and both parents to diagnose rare genetic disorders. |
Peripheral Whole Blood (3–5 mL per participant in EDTA tubes) or Saliva (Oragene OG-500 kit) | 21 Business Days | 7,500.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-668
Clopidogrel CYP2C19 Genotype Test
This test evaluates genetic variations in the CYP2C19 gene that influence the metabolism and effectiveness of the antiplatelet drug clopidogrel. |
Peripheral Whole Blood (EDTA Lavender Top Tube) | 7–10 business days | 6,000.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-672
Clostridium difficile (C. difficile) PCR Detection Test
This diagnostic test evaluates stool for the presence of the tcdB gene, a marker for toxigenic Clostridium difficile. |
Stool | 2–3 business days (batches Monday and Thursday) | 650.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
|
TEST-3453
CNGA3 Gene Achromatopsia Type 2 Genetic Test
This test identifies pathogenic variants within the CNGA3 gene associated with autosomal recessive achromatopsia type 2. |
Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card) | 3–4 Weeks | 2,800.00 AED | |
View test specifications and preparation Hide test specifications and preparation
|
||||
Category overview
Molecular Diagnostics: overview
When complex health questions arise, evaluating your health at the cellular level provides the definitive clarity necessary for proactive care. At DNA Labs UAE, our Molecular Diagnostics services harness the power of advanced nucleic acid amplification and real-time PCR technologies to detect diseases with unparalleled sensitivity. From identifying viral loads to pinpointing genetic markers, our specialized molecular testing in the UAE gives your healthcare provider the precise data needed to customize your medical strategy. Trust in one of the leading diagnostic labs in Dubai and the UAE to process your samples with rigorous confidentiality and exceptionally fast, accurate turnaround times. Step forward with absolute confidence. View our molecular diagnostics profiles below, request a seamless home sample collection, or contact our specialized team to book your test.
Before booking
Use the test details as a conversation starter
The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.
Explore this area
Related Molecular Diagnostics categories
- Genetic Disorder 2 tests
- Myopathy 1 test
- Myotonia Congenita 1 test
- Genetic Eye Diseases 1 test
- Nanopore Sequencing 1 test
- Genetic for Adrenal Hyperplasia 1 test
- NCL Panel 1 test
- Genetic for Anemia 1 test
- Neonatal Diabetes 1 test
- Genetic for Cardiac Arrhythmias 1 test
- Nephrology Genetics 1 test
- Genetic for Cardiac Disorders 1 test
- Nephrotic Syndrome Genetics 1 test
- Genetic for Cardiomyopathy 1 test
- Neuraminidase Deficiency 1 test
- Genetic for Charcot-Marie-Tooth Disease 1 test
- Genetic for Ciliary Dyskinesia 1 test
- Neurofibromatosis 2 tests
- Genetic for Connective Tissue Disorders 1 test
- Neurofibromatosis Type 1 1 test
- Genetic for Diabetes 2 tests
- Genetic for Epilepsy 1 test
- Genetic for Glaucoma 1 test
- Neurogenetic Panel 1 test
- Genetic for Hypercholesterolemia 1 test
- Genetic for Immunodeficiency 3 tests
- Neurologic Genetic Disorders 1 test
- Genetic for Kidney Disorders 1 test
- Neurological Disorders Genetics 1 test
- Genetic for MODY 1 test
- Genetic for Muscular Dystrophy 1 test
- Neurological Genetic Panel 1 test
- Genetic for Neurologic Disorders 1 test
- Genetic for Neurological Disorders 2 tests
- Neurology Genetic 1 test
- Genetic for Neuropathies 1 test
- Neuromuscular Disease Genetics 1 test
- Genetic Metabolic Disorders 3 tests
- Genetic Mutation 2 tests
- Neuromuscular Panel 1 test
- Genetic Mutation Analysis 11 tests
- Neuropathy 1 test
- Genetic Mutation Detection 1 test
- Neutropenia 1 test
- Next Generation Sequencing 5 tests
- Genetic Nephrology 1 test
- NGS Gene Panels 1 test
- Genetic Neurology 1 test
- NGS Gene Sequencing 1 test
- Genetic Neuropathy 1 test
- NGS Library Prep 1 test
- NGS Library Preparation 1 test
- Genetic Resistance 1 test
- NGS Panels 1 test
- Niemann-Pick Disease 1 test
- Genetic Skin Disorders 1 test
- Nipah Virus 1 test
- Genetic Susceptibility 7 tests
- NOD2 1 test
- Noonan Syndrome 1 test
- Genetics 1 test
- NPM1 Mutation 1 test
- Genome Sequencing 7 tests
- Nucleic Acid Extraction 2 tests
- Genomic Profiling 2 tests
- Genomic Sequencing 5 tests
- Oncogene 5 tests
- 16S rRNA Sequencing 2 tests
- Genomics 4 tests
- Oncogene Mutation 1 test
- AAT Deficiency 1 test
- Genotyping 6 tests
- Oncogene Mutation Analysis 2 tests
- Acute Myeloid Leukemia Genetic 1 test
- GIST 1 test
- Oncogenetics 6 tests
- Acute Myeloid Leukemia Genetics 1 test
- Glaucoma Genetics 1 test
- Oncogenetics Panel 1 test
- Adenovirus PCR 1 test
- Glioma Panel 1 test
- Oncologic Mutation Analysis 1 test
- Adrenal Hyperplasia 1 test
- Glucocorticoid Deficiency 1 test
- Oncology 1 test
- Oncology Genetic 3 tests
- Albinism Genetics 1 test
- Glycogen Storage Diseases 1 test
- Oncology Genetics 17 tests
- Alkaptonuria 1 test
- GMO 8 tests
- Oncology Genomics 1 test
- Alpha Thalassemia 1 test
- GMO Detection 2 tests
- Oncology Molecular 1 test
- Oncology Mutation Analysis 1 test
- Gynecological Genetics 1 test
- Oncology Mutation Panel 2 tests
- Alzheimer Disease Genetic 3 tests
- HBV Genotyping 1 test
- Oncology Panel 5 tests
- Alzheimer Disease Genetics 1 test
- HCV 1 test
- HCV Genotyping 1 test
- AML Panel 1 test
- Ancestry 1 test
- Androgen Insensitivity 1 test
- Optic Atrophy Genetic 1 test
- Anemia Genetics 1 test
- Oral Microbiology 1 test
- Angelman Syndrome 1 test
- Hematologic Malignancies 1 test
- Antiviral Resistance 1 test
- Hematologic Oncology 1 test
- Pachyonychia Congenita 1 test
- APOC2 Gene 1 test
- Hematological Disorders 1 test
- Palmoplantar Keratoderma 1 test
- APOL1 Gene 1 test
- Hematology Genetics 2 tests
- Pan-Cancer Panel 1 test
- APRT Deficiency 1 test
- Hemochromatosis 3 tests
- Pancreatitis Panel 1 test
- Aptamer Selection 1 test
- Paraganglioma Gene 1 test
- Aptamer Sequencing 1 test
- Hemoglobinopathy Screening 1 test
- Paraganglioma Genetics 1 test
- Arbovirus PCR 2 tests
- Parainfluenza Virus 1 test
- Ataxia 1 test
- Parasite 1 test
- Ataxia Genetic Panel 1 test
- Hemophilia Genetic 1 test
- Parentage 1 test
- Ataxia Panel 2 tests
- Hemophilia Panel 1 test
- Parkinson Disease 1 test
- Authentication 2 tests
- Hemorrhagic Fever Viruses 1 test
- Parkinson's Disease Genetic 1 test
- Autoimmune Genetics 1 test
- Hepatitis B Genotyping 1 test
- Parkinson's Disease Genetics 2 tests
- AVPR2 Gene 1 test
- Hepatitis B Panel 1 test
- Parkinson's Genetic 1 test
- Hepatitis B Viral Load 1 test
- Parvovirus B19 2 tests
- Hepatitis C 9 tests
- Paternity 4 tests
- Bacterial Typing 1 test
- Hepatitis C Genotyping 1 test
- Paternity and Relationship DNA 1 test
- Hepatitis D 1 test
- BCR-ABL 6 tests
- Hepatitis E 2 tests
- Pendred Syndrome 1 test
- BCR-ABL Quantitation 1 test
- Hepatitis G Virus 1 test
- BCR-ABL1 1 test
- HER2 2 tests
- Pharmacogenetics 11 tests
- BCR-ABL1 Mutation Analysis 2 tests
- Bioinformatics 1 test
- Hereditary Cancer Genetics 4 tests
- Pheochromocytoma Genetic 1 test
- BK Virus 1 test
- Hereditary Cancer Panel 3 tests
- Pheochromocytoma Genetics 1 test
- Bocavirus 1 test
- Piebaldism 1 test
- Bone Disorders 1 test
- Pigmentary Disorders 1 test
- Bone Marrow Failure 1 test
- Pituitary Adenoma Genetics 1 test
- Bovine Genotyping 1 test
- Hereditary Hearing Loss Genetic Panel 1 test
- BRAF Mutation 2 tests
- Hereditary Hematologic Disorders 1 test
- BRCA Gene 1 test
- Hereditary Hemochromatosis 2 tests
- Breast Cancer 1 test
- Hereditary Prostate Cancer 1 test
- Preimplantation Genetic 1 test
- Hereditary Retinal Diseases 1 test
- Hereditary Retinal Dystrophy 1 test
- CALR Gene 1 test
- Hereditary Retinoblastoma 1 test
- CALR Mutation 1 test
- Hereditary Skin Disorders 1 test
- Cancer Gene Panel 6 tests
- Cancer Gene Panels 3 tests
- Hereditary Spherocytosis 2 tests
- Primary Ciliary Dyskinesia Genetics 1 test
- Hereditary Stomatocytosis 1 test
- Hereditary Syndromes 1 test
- Primary Immunodeficiency Genetic 2 tests
- Cancer Genomic Profiling 1 test
- Herpes Simplex Virus 4 tests
- Primary Immunodeficiency Genetics 1 test
- Cancer Genomics 3 tests
- Herpesvirus Detection 1 test
- Progressive Intrahepatic Cholestasis 1 test
- Cancer Genomics Panel 1 test
- HEV Viral Load 1 test
- Prostate Cancer Screening 1 test
- Cancer Mutation Panel 5 tests
- Hi-C Sequencing 1 test
- Psoriasis Genetic 1 test
- Pulmonary Fibrosis Genetics 1 test
- Cancer Panels 3 tests
- HIV Genotyping and Resistance 1 test
- Rabies 2 tests
- Cancer Predisposition Genetic 1 test
- Rare Genetic Disease 1 test
- Cancer Screening 1 test
- RAS Mutation Panel 2 tests
- Cancer Susceptibility 1 test
- HLA-B27 1 test
- Recurrent Pregnancy Loss Genetics 1 test
- Cardiac Genetic 3 tests
- Homologous Recombination Deficiency 1 test
- Relationship DNA 3 tests
- Cardiac Genetics Panel 1 test
- HPV 4 tests
- Renal Genetics 1 test
- Cardiogenetic 1 test
- HPV Genotyping 1 test
- Cardiogenetics 6 tests
- HSV PCR 1 test
- Respiratory Infection Panel 1 test
- Cardiomyopathy 2 tests
- Human Herpesvirus 1 test
- Hyperchylomicronemia Genetic 1 test
- Respiratory Virus 1 test
- Hypertrophic Cardiomyopathy 1 test
- Respiratory Virus Detection 1 test
- Hypobetalipoproteinemia 1 test
- Hypotrichosis 2 tests
- Retinal Dystrophy Genetic 1 test
- Cataract Genetics 1 test
- CCHS Genetic 1 test
- Cell Line Authentication 1 test
- Ichthyosis Vulgaris 1 test
- RNA Extraction 3 tests
- IGHV Mutation Status 1 test
- RNA Sequencing 14 tests
- Charcot-Marie-Tooth Genetic 1 test
- IgVH Mutation Analysis 1 test
- Chemotherapy Sensitivity 1 test
- Salmonella Typhi 1 test
- Chikungunya 1 test
- Immunodeficiency Gene Sequencing 1 test
- Sandhoff Disease 1 test
- Chikungunya Virus 1 test
- Sarcoma Panel 1 test
- Chimerism 2 tests
- SCA 1 test
- Chimerism Analysis 4 tests
- Chimerism Study 1 test
- Sequencing Analysis 1 test
- In Situ Hybridization 1 test
- Chromatin Accessibility 1 test
- Infectious Disease PCR 5 tests
- Sequencing Library Preparation 1 test
- Chromatin Analysis 2 tests
- Infertility Genetics 1 test
- Chromatin Conformation 1 test
- Sickle Cell 1 test
- Chromatin Conformation Analysis 1 test
- Influenza PCR 1 test
- Sickle Cell Disease 1 test
- Influenza Viral Load 1 test
- Silver-Russell Syndrome 1 test
- Inherited Anemias 1 test
- Inherited Cardiac Arrhythmia 1 test
- Ciliopathy 1 test
- Inherited Disease Panel 1 test
- CLL Prognostic Panel 1 test
- Clonality 1 test
- Clostridium difficile 1 test
- Inherited Retinal Diseases 1 test
- Inherited Retinal Disorders 1 test
- Skeletal Dysplasia Genetic 1 test
- CMT1A Genetic 1 test
- Inherited Retinal Dystrophies 3 tests
- SMA 2 tests
- CMV PCR 1 test
- Solid Tumor Panel 1 test
- CMV Viral Load 1 test
- Inherited Thrombocytopenia 1 test
- Solid Tumor Profiling 1 test
- Intellectual Disability Panel 1 test
- Species Identification 4 tests
- Coagulation Factor Deficiencies 1 test
- Iron-Refractory Anemia 1 test
- Spinal Muscular Atrophy 4 tests
- Comprehensive Genomic Profiling 1 test
- JAK2 Mutation 5 tests
- Congenital Disorders of Glycosylation 2 tests
- JAK2 Mutation Analysis 3 tests
- Spinocerebellar Ataxia Genetic 1 test
- Congenital Myasthenic Syndrome 3 tests
- JAK2 Mutations 1 test
- Copy Number Variation 1 test
- Kallmann Syndrome 1 test
- STI PCR 2 tests
- KIT Mutation 1 test
- Coronaviruses 1 test
- KRAS Mutation 2 tests
- Targeted Gene Sequencing 2 tests
- COVID-19 1 test
- Lafora Disease Genetic 1 test
- Targeted Sequencing 1 test
- CPA1 Gene Mutation 1 test
- LDLR Gene Mutation 1 test
- TB 1 test
- Leigh Syndrome Genetics 1 test
- CYP2C19 Genotyping 1 test
- Telomere 1 test
- Cystic Fibrosis 4 tests
- Leukemia FISH 1 test
- Thalassemia Genetics 2 tests
- Cystinuria 2 tests
- Leukemia Fusion Gene Analysis 1 test
- Thalassemia Mutation Panel 1 test
- Leukemia Fusion Genes 1 test
- Thalassemia Panel 1 test
- Leukemia Gene Fusion 1 test
- Leukemia Gene Rearrangements 1 test
- Delta-Beta Thalassemia 1 test
- Leukemia Genetic 2 tests
- Thrombophilia Genetic 1 test
- Leukemia Genetic Panel 1 test
- Thrombophilia Genetics 2 tests
- Dengue PCR 1 test
- Thrombophilia Genotyping 1 test
- Thrombophilia Mutation 1 test
- Diabetes Genetics 1 test
- Leukemia Mutation Analysis 1 test
- Leukemia Mutations 1 test
- Thyroid Cancer Genetics 1 test
- DNA 2 tests
- Thyroid Cancer Panels 1 test
- DNA Analysis 1 test
- Thyroid Genetic 4 tests
- Leukemia PCR 2 tests
- TMB and MSI 1 test
- DNA Methylation 3 tests
- Leukocyte Adhesion Deficiency 1 test
- DNA Methylation Analysis 5 tests
- Library Preparation 5 tests
- Transcriptome Analysis 1 test
- Limb-Girdle Muscular Dystrophy 3 tests
- Transcriptome Sequencing 2 tests
- DNA Relationship 2 tests
- Lipoprotein Disorders 1 test
- Transcriptomics 6 tests
- DNA Sequencing 8 tests
- Liquid Biopsy 5 tests
- TTV 1 test
- Dystonia 1 test
- Dystonia Genetic 2 tests
- Long QT Syndrome Genetic 1 test
- Tuberculosis Drug Resistance 1 test
- Ectodermal Dysplasia 1 test
- EGFR 3 tests
- Tumor Profiling 3 tests
- EGFR Mutation 1 test
- Lynch Syndrome 2 tests
- Uniparental Disomy 1 test
- ENT Genetic Panel 1 test
- Vector-Borne Viral Panel 1 test
- Enzyme Panel 1 test
- Malaria PCR 2 tests
- Epigenetics 4 tests
- Male Fertility 1 test
- Viral Genomics 1 test
- Epigenomics 1 test
- Epilepsy Gene Panel 2 tests
- Marfan Syndrome 1 test
- Viral Metagenomics 1 test
- MED25 Gene 1 test
- Viral Panel 2 tests
- Megaloblastic Anemia Genetic 1 test
- Epilepsy Panel 1 test
- Melanoma Genetic 1 test
- Viral RNA Detection 3 tests
- MEN1 1 test
- Viral Sequencing 1 test
- Exome Sequencing 12 tests
- Meningioma Genetic 1 test
- Meningitis Panel 1 test
- von Willebrand Disease 1 test
- Fanconi Anemia Panel 1 test
- VZV PCR 1 test
- FGFR2 Gene 2 tests
- Metabolic Disorders Panel 1 test
- West Nile Virus 1 test
- Whole Genome Sequencing (Bacterial) 1 test
- Williams-Beuren Syndrome 1 test
- FLT3 Mutation 2 tests
- Y Chromosome Microdeletion 3 tests
- FLT3 Mutations 1 test
- Methylation Analysis 1 test
- Methylmalonic Aciduria 1 test
- Fragile X 1 test
- Fungal Detection 1 test
- Microbial Genome Sequencing 1 test
- Fungal Panel 1 test
- Mineralization Disorders 1 test
- Fungal Sequencing 1 test
- Mitochondrial 1 test
- Fusion Gene 1 test
- Mitochondrial Diseases 1 test
- Fusion Gene Analysis 1 test
- Mitochondrial Disorder 1 test
- Fusion Gene Detection 2 tests
- Fusion Transcript PCR 1 test
- Mitochondrial Gene Sequencing 1 test
- G6PD Deficiency 1 test
- G6PD Genetic 1 test
- MODY 4 tests
- Gaucher Disease 3 tests
- MODY Genetic 3 tests
- Gaucher Disease Genetic 1 test
- MODY Panel 1 test
- Gene Analysis 1 test
- Monogenic Diabetes Genetic 1 test
- Gene Expression 3 tests
- Gene Expression Analysis 1 test
- MPN Mutation Panel 1 test
- Gene Fusion 1 test
- MPN Panel 2 tests
- Gene Fusion Panels 1 test
- MRD Monitoring 2 tests
- Gene Load 1 test
- MSI 1 test
- Gene Mutation 1 test
- MTHFR Gene Mutation 1 test
- Gene Panel 3 tests
- Gene Panels 2 tests
- Multiple Myeloma Genetics 1 test
- Gene Quantification 2 tests
- Gene Rearrangement 5 tests
- Gene-Specific 1 test
- Muscular Dystrophy Panel 2 tests
- Mutation Analysis 2 tests
- Genetic - Single Gene 2 tests
- Myasthenic Syndrome 1 test
- Genetic Abnormalities 1 test
- Genetic Cardiac 1 test
- Myelodysplastic Syndrome 1 test
- Genetic Cardiomyopathy 1 test
- Myeloid Leukemia Genetics 1 test
- Genetic Cardiovascular 1 test
- Myeloid Panel 2 tests
- Genetic Carrier 1 test
- Myeloproliferative Disorder 1 test
- Genetic Carrier Screening 1 test
- Myeloproliferative Disorders 2 tests
- Myeloproliferative Neoplasm Panel 1 test
- Genetic Diabetes 2 tests
- MYH7 Gene 1 test