| التحليل / Test | التصنيف / Category | العينة / Sample | الأيام / Days | المرجع / Reference | السعر / Price | تفاصيل / Details | طلب / Request |
| ALK Rearrangement Test | Molecular Oncology | Tumor Tissue / FFPE | 10 | ALK rearrangement not detected. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Alport Syndrome Panel | Nephrogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,800.00 | تفاصيل / Details | طلب / Request |
| Array CGH / SNP Array | Cytogenetics and Chromosomal Testing | Blood / Tissue | 21 | No clinically significant copy number change detected. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Autism Spectrum Disorder Genetic Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,400.00 | تفاصيل / Details | طلب / Request |
| Avuncular DNA Test | DNA Relationship Testing | Buccal Swab | 7 | Relationship likelihood calculated from genetic markers. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Basic Carrier Screening Panel | Carrier Screening | Blood / Saliva | 14 | No pathogenic carrier variants identified in tested genes. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Biotinidase Deficiency - BTD Test | Newborn Screening | Blood / Dried Blood Spot | 14 | No pathogenic BTD variant detected. | 1,500.00 | تفاصيل / Details | طلب / Request |
| BRAF V600 Mutation Test | Molecular Oncology | Tumor Tissue / Plasma | 7 | BRAF V600 mutation not detected. | 1,600.00 | تفاصيل / Details | طلب / Request |
| BRCA1/BRCA2 Hereditary Breast and Ovarian Cancer Test | Cancer Genetic Testing | Blood / Saliva | 14 | No pathogenic or likely pathogenic variant detected. | 2,500.00 | تفاصيل / Details | طلب / Request |
| Brugada Syndrome Panel | Cardiogenetics | Blood / Saliva | 21 | No pathogenic variant detected in tested genes. | 4,200.00 | تفاصيل / Details | طلب / Request |
| CALR Mutation Test | Hematogenetics and Thrombophilia | Blood / Bone Marrow | 10 | CALR mutation not detected. | 1,600.00 | تفاصيل / Details | طلب / Request |
| Carrier Screening Panel | Carrier Screening | Blood / Saliva | 14 | No pathogenic carrier variants identified in tested genes. | 2,200.00 | تفاصيل / Details | طلب / Request |
| CFTR Cystic Fibrosis Mutation Test | Carrier Screening | Blood / Buccal Swab | 10 | No pathogenic CFTR variant detected. | 1,300.00 | تفاصيل / Details | طلب / Request |
| Chromosomal Microarray Analysis | Rare Disease Testing | Blood | 21 | No clinically significant copy number gain or loss detected. | 3,800.00 | تفاصيل / Details | طلب / Request |
| Complete Blood Count - CBC | Hematology | Whole Blood | 1 | According to age and sex reference range. | 180.00 | تفاصيل / Details | طلب / Request |
| Congenital Adrenal Hyperplasia - CYP21A2 Test | Endocrine and Metabolic Genetics | Blood / Saliva | 21 | No pathogenic CYP21A2 variant detected. | 3,500.00 | تفاصيل / Details | طلب / Request |
| CYP2C19 Genotyping | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal metabolizer genotype, commonly *1/*1 when applicable. | 900.00 | تفاصيل / Details | طلب / Request |
| CYP2C9 and VKORC1 Warfarin Sensitivity Test | Pharmacogenomics | Blood / Buccal Swab | 7 | Standard sensitivity genotype when no risk alleles are detected. | 1,100.00 | تفاصيل / Details | طلب / Request |
| CYP2D6 Genotyping and Copy Number | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal metabolizer activity score according to detected genotype. | 950.00 | تفاصيل / Details | طلب / Request |
| Dilated Cardiomyopathy Panel | Cardiogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,800.00 | تفاصيل / Details | طلب / Request |
| DPYD Fluoropyrimidine Toxicity Test | Pharmacogenomics | Blood / Buccal Swab | 7 | No tested DPYD decreased-function variant detected. | 1,200.00 | تفاصيل / Details | طلب / Request |
| Duchenne Muscular Dystrophy Carrier Test - DMD | Carrier Screening | Blood | 21 | No pathogenic DMD variant or deletion/duplication detected. | 3,000.00 | تفاصيل / Details | طلب / Request |
| EGFR Mutation Test | Molecular Oncology | Tumor Tissue / Plasma | 7 | No reportable EGFR mutation detected. | 1,800.00 | تفاصيل / Details | طلب / Request |
| Epidermolysis Bullosa Panel | Dermatogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Epilepsy Genetic Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested epilepsy genes. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Expanded Carrier Screening Panel | Carrier Screening | Blood / Saliva | 21 | No pathogenic carrier variants identified in tested genes. | 4,500.00 | تفاصيل / Details | طلب / Request |
| Factor V Leiden Mutation Test | Hematogenetics and Thrombophilia | Blood / Buccal Swab | 7 | Factor V Leiden variant not detected. | 700.00 | تفاصيل / Details | طلب / Request |
| Familial Adenomatous Polyposis - APC Test | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic APC variant detected. | 2,700.00 | تفاصيل / Details | طلب / Request |
| Familial Hypercholesterolemia Panel | Cardiogenetics | Blood / Saliva | 21 | No pathogenic variant detected in tested genes. | 3,800.00 | تفاصيل / Details | طلب / Request |
| Familial Hyperinsulinism Panel | Endocrine and Metabolic Genetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,000.00 | تفاصيل / Details | طلب / Request |
| Familial Mediterranean Fever - MEFV Test | Carrier Screening | Blood / Saliva | 14 | No pathogenic MEFV variant detected. | 1,400.00 | تفاصيل / Details | طلب / Request |
| Fasting Blood Glucose | Clinical Chemistry | Serum / Plasma | 1 | 70 - 99 mg/dL. | 90.00 | تفاصيل / Details | طلب / Request |
| Fetal RHD Genotyping | Prenatal Genetic Testing | Maternal Blood | 10 | Fetal RHD not detected when applicable. | 1,600.00 | تفاصيل / Details | طلب / Request |
| FISH Aneuploidy Panel | Cytogenetics and Chromosomal Testing | Blood / Amniotic Fluid / Tissue | 7 | No tested aneuploidy detected. | 1,800.00 | تفاصيل / Details | طلب / Request |
| FISH Microdeletion Panel | Cytogenetics and Chromosomal Testing | Blood | 10 | No tested microdeletion detected. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Fragile X - FMR1 CGG Repeat Analysis | Rare Disease Testing | Blood | 14 | Normal range: approximately 5 to 44 CGG repeats. | 1,800.00 | تفاصيل / Details | طلب / Request |
| Fragile X Premutation Carrier Test - FMR1 | Carrier Screening | Blood | 14 | Normal range: approximately 5 to 44 CGG repeats. | 1,800.00 | تفاصيل / Details | طلب / Request |
| G6PD Gene Mutation Test | Carrier Screening | Blood / Buccal Swab | 10 | No tested pathogenic G6PD variant detected. | 900.00 | تفاصيل / Details | طلب / Request |
| GALT Galactosemia Genetic Test | Newborn Screening | Blood / Dried Blood Spot | 14 | No pathogenic GALT variant detected. | 1,600.00 | تفاصيل / Details | طلب / Request |
| Grandparent DNA Test | DNA Relationship Testing | Buccal Swab | 7 | Relationship likelihood calculated from genetic markers. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Hearing Loss Newborn Genetic Panel | Newborn Screening | Blood / Buccal Swab | 21 | No pathogenic variant detected in tested hearing loss genes. | 3,200.00 | تفاصيل / Details | طلب / Request |
| Hemophilia A Carrier Test - F8 | Carrier Screening | Blood | 21 | No pathogenic F8 variant detected. | 2,800.00 | تفاصيل / Details | طلب / Request |
| Hemophilia B Carrier Test - F9 | Carrier Screening | Blood | 21 | No pathogenic F9 variant detected. | 2,600.00 | تفاصيل / Details | طلب / Request |
| Hereditary Cancer Panel | Cancer Genetic Testing | Blood / Saliva | 21 | No clinically significant pathogenic variant detected. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Hereditary Pancreatic Cancer Panel | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic or likely pathogenic variant detected. | 3,700.00 | تفاصيل / Details | طلب / Request |
| Hereditary Prostate Cancer Panel | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic or likely pathogenic variant detected. | 3,600.00 | تفاصيل / Details | طلب / Request |
| HLA Typing - High Resolution | HLA and Immunogenetics | Blood / Buccal Swab | 14 | HLA genotype reported according to tested loci. | 4,500.00 | تفاصيل / Details | طلب / Request |
| HLA Typing - Low Resolution | HLA and Immunogenetics | Blood / Buccal Swab | 10 | HLA genotype reported according to tested loci. | 2,200.00 | تفاصيل / Details | طلب / Request |
| HLA-A*31:01 Screening | Pharmacogenomics | Blood / Buccal Swab | 7 | Negative for HLA-A*31:01 allele. | 800.00 | تفاصيل / Details | طلب / Request |
| HLA-B*15:02 Screening | Pharmacogenomics | Blood / Buccal Swab | 7 | Negative for HLA-B*15:02 allele. | 800.00 | تفاصيل / Details | طلب / Request |
| HLA-B*57:01 Screening | Pharmacogenomics | Blood / Buccal Swab | 7 | Negative for HLA-B*57:01 allele. | 800.00 | تفاصيل / Details | طلب / Request |
| HLA-B27 Test | HLA and Immunogenetics | Blood / Buccal Swab | 7 | HLA-B27 not detected. | 900.00 | تفاصيل / Details | طلب / Request |
| HLA-DQ2/DQ8 Celiac Disease Test | HLA and Immunogenetics | Blood / Buccal Swab | 7 | HLA-DQ2/DQ8 not detected. | 1,100.00 | تفاصيل / Details | طلب / Request |
| Hypertrophic Cardiomyopathy Panel | Cardiogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,800.00 | تفاصيل / Details | طلب / Request |
| Ichthyosis Genetic Panel | Dermatogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,000.00 | تفاصيل / Details | طلب / Request |
| Inherited Cardiac Disease Panel | Cardiogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested cardiac genes. | 5,600.00 | تفاصيل / Details | طلب / Request |
| Inherited Kidney Disease Panel | Nephrogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,600.00 | تفاصيل / Details | طلب / Request |
| Inherited Metabolic Disorders Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,800.00 | تفاصيل / Details | طلب / Request |
| Inherited Retinal Disease Panel | Ophthalmogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,600.00 | تفاصيل / Details | طلب / Request |
| Intellectual Disability and Developmental Delay Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,600.00 | تفاصيل / Details | طلب / Request |
| JAK2 V617F Mutation Test | Hematogenetics and Thrombophilia | Blood / Bone Marrow | 7 | JAK2 V617F mutation not detected. | 1,500.00 | تفاصيل / Details | طلب / Request |
| Karyotype Analysis - Blood | Cytogenetics and Chromosomal Testing | Blood | 14 | Normal chromosomal complement. | 1,800.00 | تفاصيل / Details | طلب / Request |
| KRAS/NRAS Mutation Test | Molecular Oncology | Tumor Tissue / Plasma | 7 | No reportable KRAS/NRAS mutation detected. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Leber Congenital Amaurosis Panel | Ophthalmogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Liquid Biopsy ctDNA Panel | Cancer Genetic Testing | Blood | 14 | No reportable ctDNA variant detected in tested regions. | 7,000.00 | تفاصيل / Details | طلب / Request |
| Liver Function Tests | Clinical Chemistry | Serum | 1 | According to lab reference range. | 250.00 | تفاصيل / Details | طلب / Request |
| Long QT Syndrome Panel | Cardiogenetics | Blood / Saliva | 21 | No pathogenic variant detected in tested genes. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Lynch Syndrome Panel - MLH1/MSH2/MSH6/PMS2/EPCAM | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic Lynch syndrome-related variant detected. | 3,800.00 | تفاصيل / Details | طلب / Request |
| Male Infertility Genetic Panel | Reproductive Genetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Male Infertility Y Chromosome Microdeletion Test | Reproductive Genetics | Blood / Buccal Swab | 14 | No AZF microdeletion detected. | 1,800.00 | تفاصيل / Details | طلب / Request |
| Maternity DNA Test - STR Profile | DNA Relationship Testing | Buccal Swab | 7 | Inclusion reference: probability of maternity usually greater than 99.9%. | 1,600.00 | تفاصيل / Details | طلب / Request |
| Maturity-Onset Diabetes of the Young - MODY Panel | Endocrine and Metabolic Genetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,800.00 | تفاصيل / Details | طلب / Request |
| Mitochondrial Genome Sequencing | Rare Disease Testing | Blood / Buccal Swab | 30 | No pathogenic mitochondrial DNA variant detected. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Monogenic Obesity Panel | Endocrine and Metabolic Genetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,800.00 | تفاصيل / Details | طلب / Request |
| MPL Mutation Test | Hematogenetics and Thrombophilia | Blood / Bone Marrow | 10 | MPL mutation not detected. | 1,600.00 | تفاصيل / Details | طلب / Request |
| MSI / MMR Molecular Test | Molecular Oncology | Tumor Tissue / Blood | 10 | Microsatellite stable / no abnormality detected when applicable. | 2,500.00 | تفاصيل / Details | طلب / Request |
| mtDNA Maternal Lineage Test | DNA Relationship Testing | Buccal Swab / Blood | 14 | mtDNA haplotypes compared for maternal lineage consistency. | 2,800.00 | تفاصيل / Details | طلب / Request |
| MTHFR C677T/A1298C Mutation Test | Rare Disease Testing | Blood / Buccal Swab | 7 | Wild type: C677C and A1298A. | 700.00 | تفاصيل / Details | طلب / Request |
| MUTYH-Associated Polyposis Test | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic MUTYH variant detected. | 2,300.00 | تفاصيل / Details | طلب / Request |
| Neuromuscular Disorders Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,500.00 | تفاصيل / Details | طلب / Request |
| Newborn Genetic Screening Panel | Newborn Screening | Dried Blood Spot / Blood | 14 | No pathogenic variants detected in screened genes. | 2,800.00 | تفاصيل / Details | طلب / Request |
| Newborn Metabolic Disease Gene Panel | Newborn Screening | Blood / Dried Blood Spot | 21 | No pathogenic variants detected in tested genes. | 4,200.00 | تفاصيل / Details | طلب / Request |
| NIPT - Trisomy 21/18/13 Screening | Prenatal Genetic Testing | Maternal Blood | 10 | Low risk for Trisomy 21, Trisomy 18, and Trisomy 13. | 3,000.00 | تفاصيل / Details | طلب / Request |
| NIPT Expanded Aneuploidy Screening | Prenatal Genetic Testing | Maternal Blood | 12 | Low risk for screened aneuploidies. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Oculocutaneous Albinism Panel | Dermatogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,600.00 | تفاصيل / Details | طلب / Request |
| Optic Atrophy Genetic Panel | Ophthalmogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,000.00 | تفاصيل / Details | طلب / Request |
| Paternity DNA Test - STR Profile | DNA Relationship Testing | Buccal Swab | 7 | Inclusion reference: probability of paternity usually greater than 99.9%. | 1,600.00 | تفاصيل / Details | طلب / Request |
| PGT-A Preimplantation Genetic Testing for Aneuploidy | Reproductive Genetics | Embryo Biopsy | 14 | Euploid result when no tested aneuploidy is detected. | 6,500.00 | تفاصيل / Details | طلب / Request |
| PGT-M Monogenic Disorder Testing | Reproductive Genetics | Embryo Biopsy | 21 | Familial pathogenic variant not detected. | 9,000.00 | تفاصيل / Details | طلب / Request |
| PGT-SR Structural Rearrangement Testing | Reproductive Genetics | Embryo Biopsy | 21 | Balanced/normal result according to tested rearrangement. | 8,500.00 | تفاصيل / Details | طلب / Request |
| Pharmacogenomics Comprehensive Panel | Pharmacogenomics | Blood / Buccal Swab | 14 | Drug response interpretation depends on detected genotype. | 3,500.00 | تفاصيل / Details | طلب / Request |
| Pharmacogenomics CYP2C19 Test | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal metabolizer genotype, commonly *1/*1 when applicable. | 900.00 | تفاصيل / Details | طلب / Request |
| Pharmacogenomics CYP2D6 Test | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal metabolizer activity score according to detected genotype. | 950.00 | تفاصيل / Details | طلب / Request |
| POI Premature Ovarian Insufficiency Panel | Reproductive Genetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 4,500.00 | تفاصيل / Details | طلب / Request |
| Polycystic Kidney Disease Panel - PKD1/PKD2 | Nephrogenetics | Blood / Saliva | 30 | No pathogenic PKD1/PKD2 variant detected. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Prenatal Chromosomal Microarray | Prenatal Genetic Testing | Amniotic Fluid / CVS | 21 | No clinically significant copy number gain or loss detected. | 4,500.00 | تفاصيل / Details | طلب / Request |
| Prenatal Karyotype Analysis | Prenatal Genetic Testing | Amniotic Fluid / CVS | 14 | Normal chromosomal complement. | 2,500.00 | تفاصيل / Details | طلب / Request |
| Primary Immunodeficiency Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,800.00 | تفاصيل / Details | طلب / Request |
| Products of Conception Genetic Testing | Cytogenetics and Chromosomal Testing | POC Tissue | 21 | No clinically significant chromosomal abnormality detected. | 4,200.00 | تفاصيل / Details | طلب / Request |
| Prothrombin G20210A Mutation Test | Hematogenetics and Thrombophilia | Blood / Buccal Swab | 7 | Prothrombin G20210A variant not detected. | 700.00 | تفاصيل / Details | طلب / Request |
| PTEN Cowden Syndrome Test | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic PTEN variant detected. | 2,500.00 | تفاصيل / Details | طلب / Request |
| Rapid Prenatal Aneuploidy QF-PCR | Prenatal Genetic Testing | Amniotic Fluid / CVS | 5 | No evidence of tested trisomy or sex chromosome aneuploidy. | 1,600.00 | تفاصيل / Details | طلب / Request |
| RET MEN2 / Medullary Thyroid Cancer Test | Cancer Genetic Testing | Blood / Saliva | 14 | No pathogenic RET variant detected. | 2,300.00 | تفاصيل / Details | طلب / Request |
| Retinitis Pigmentosa Panel | Ophthalmogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,200.00 | تفاصيل / Details | طلب / Request |
| ROS1 Rearrangement Test | Molecular Oncology | Tumor Tissue / FFPE | 10 | ROS1 rearrangement not detected. | 2,200.00 | تفاصيل / Details | طلب / Request |
| SCID Newborn Genetic Test | Newborn Screening | Blood / Dried Blood Spot | 21 | No pathogenic variant detected in tested genes. | 3,500.00 | تفاصيل / Details | طلب / Request |
| Sibling DNA Test | DNA Relationship Testing | Buccal Swab | 7 | Relationship likelihood calculated from genetic markers. | 2,200.00 | تفاصيل / Details | طلب / Request |
| Single Gene Prenatal Diagnosis | Prenatal Genetic Testing | Amniotic Fluid / CVS | 14 | Familial pathogenic variant not detected. | 3,000.00 | تفاصيل / Details | طلب / Request |
| Skeletal Dysplasia Panel | Rare Disease Testing | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,500.00 | تفاصيل / Details | طلب / Request |
| SLCO1B1 Statin Myopathy Risk Test | Pharmacogenomics | Blood / Buccal Swab | 7 | No increased-risk SLCO1B1 genotype detected. | 900.00 | تفاصيل / Details | طلب / Request |
| SMA - SMN1 Copy Number Test | Carrier Screening | Blood / Saliva | 10 | SMN1 copy number: 2 or more copies. | 1,400.00 | تفاصيل / Details | طلب / Request |
| Steroid Resistant Nephrotic Syndrome Panel | Nephrogenetics | Blood / Saliva | 30 | No pathogenic variant detected in tested genes. | 5,200.00 | تفاصيل / Details | طلب / Request |
| Thalassemia Alpha Globin Gene Test - HBA1/HBA2 | Carrier Screening | Blood | 14 | No pathogenic alpha globin deletion or variant detected. | 1,500.00 | تفاصيل / Details | طلب / Request |
| Thalassemia Beta Globin Gene Test - HBB | Carrier Screening | Blood | 14 | No pathogenic HBB variant detected. | 1,500.00 | تفاصيل / Details | طلب / Request |
| Thrombophilia Genetic Panel | Hematogenetics and Thrombophilia | Blood / Buccal Swab | 10 | No tested thrombophilia risk variant detected. | 1,800.00 | تفاصيل / Details | طلب / Request |
| TP53 Li-Fraumeni Syndrome Test | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic TP53 variant detected. | 2,600.00 | تفاصيل / Details | طلب / Request |
| TPMT and NUDT15 Thiopurine Sensitivity Test | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal metabolizer genotype when no decreased-function allele is detected. | 1,300.00 | تفاصيل / Details | طلب / Request |
| Trio Whole Exome Sequencing | Rare Disease Testing | Blood / Saliva | 45 | No pathogenic or likely pathogenic variant related to the indication detected. | 18,000.00 | تفاصيل / Details | طلب / Request |
| Tumor NGS Solid Tumor Panel | Cancer Genetic Testing | Tumor Tissue / FFPE | 21 | No reportable clinically significant variant detected in tested regions. | 6,500.00 | تفاصيل / Details | طلب / Request |
| UGT1A1 Irinotecan Toxicity Test | Pharmacogenomics | Blood / Buccal Swab | 7 | Normal UGT1A1 activity genotype when applicable. | 1,000.00 | تفاصيل / Details | طلب / Request |
| VHL Disease Genetic Test | Cancer Genetic Testing | Blood / Saliva | 21 | No pathogenic VHL variant detected. | 2,400.00 | تفاصيل / Details | طلب / Request |
| Whole Exome Sequencing | Rare Disease Testing | Blood / Saliva | 45 | No pathogenic or likely pathogenic variant related to the indication detected. | 8,500.00 | تفاصيل / Details | طلب / Request |
| Whole Genome Sequencing | Rare Disease Testing | Blood / Saliva | 60 | No pathogenic or likely pathogenic variant related to the indication detected. | 15,000.00 | تفاصيل / Details | طلب / Request |
| Y-STR Paternal Lineage Test | DNA Relationship Testing | Buccal Swab / Blood | 10 | Y-STR haplotypes compared for paternal lineage consistency. | 2,500.00 | تفاصيل / Details | طلب / Request |