| BRCA1 & BRCA2 | 
      Genetic | 
      Breast Cancer Risk | 
      General | 
      Breast and Ovarian Cancer | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | 23andMe Ancestry | 
      Ancestry | 
      Genetic Ancestry | 
      General | 
      Trait Analysis | 
      23andMe | 
      Not Required | 
    
    
      | Genetic Carrier Screening | 
      Carrier | 
      Carrier Status | 
      General | 
      Cystic Fibrosis, SMA | 
      Invitae | 
      FDA Approved | 
    
    
      | Clarity Genetic Test | 
      Diagnostic | 
      Hereditary Cancer | 
      Family | 
      Various Cancers | 
      Invitae | 
      FDA Approved | 
    
    
      | Cardio genomic panel | 
      Genetic | 
      Cardiovascular Disease | 
      Cardiac | 
      Hypertrophic Cardiomyopathy | 
      GeneDx | 
      FDA Approved | 
    
    
      | Whole Exome Sequencing | 
      Genetic | 
      Rare Disease Diagnosis | 
      General | 
      Various Rare Diseases | 
      Ambry Genetics | 
      Research Use | 
    
    
      | ExomePlus | 
      Genetic | 
      Hereditary Disorder | 
      General | 
      Genetic Syndromes | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | PGT-M | 
      Reproductive | 
      Embryo Testing | 
      Pregnant | 
      Genetic Disorders | 
      Natera | 
      FDA Approved | 
    
    
      | MTHFR Gene Test | 
      Genetic | 
      Thrombophilia Risk | 
      General | 
      MTHFR Mutation Effects | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genomic Health BreastRecurrence Score | 
      Diagnostic | 
      Breast Cancer Recurrence | 
      Oncology | 
      Breast Cancer Risk | 
      Genomic Health | 
      FDA Approved | 
    
    
      | Carrier Screening for 50 Diseases | 
      Carrier | 
      Carrier Status | 
      General | 
      Various Genetic Disorders | 
      Fulgent Genetics | 
      FDA Approved | 
    
    
      | Actionable Insights for Hereditary Cancer | 
      Diagnostic | 
      Hereditary Cancer Risk | 
      Family | 
      Various Cancers | 
      Foundation Medicine | 
      FDA Approved | 
    
    
      | Disease-Specific Panels | 
      Genetic | 
      Specific Conditions | 
      Special Population | 
      Specific Rare Diseases | 
      Multiple Labs | 
      Research Use | 
    
    
      | Familial Hypercholesterolemia Testing | 
      Genetic | 
      Cholesterol Disorders | 
      General | 
      Heart Disease Risk | 
      Various Labs | 
      FDA Approved | 
    
    
      | SNP Testing | 
      Ancestry | 
      Genetic Variants | 
      General | 
      Trait Analysis | 
      23andMe | 
      Not Required | 
    
    
      | Neurogenetics Panel | 
      Genetic | 
      Neurological Disorders | 
      General | 
      Neurodegenerative Diseases | 
      GeneDx | 
      FDA Approved | 
    
    
      | Pharmacogenomic Testing | 
      Pharmacogenomic | 
      Drug Response | 
      General | 
      Medication Metabolism | 
      Various Labs | 
      FDA Approved | 
    
    
      | Ancestry Composition Report | 
      Ancestry | 
      Ethnic Ancestry Composition | 
      General | 
      Genetic Traits | 
      Ancestry.com | 
      Not Required | 
    
    
      | Hemoglobinopathies Testing | 
      Carrier | 
      Sickle Cell Anemia, Thalassemia | 
      Ethnic Groups | 
      Sickle Cell Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Prenatal Genetic Testing | 
      Prenatal | 
      Fetal Genetic Conditions | 
      Pregnant | 
      Chromosomal Abnormalities | 
      Natera | 
      FDA Approved | 
    
    
      | Next Generation Sequencing Panels | 
      Genetic | 
      Broad Genetic Conditions | 
      General | 
      Various Genetic Disorders | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Hereditary Hemochromatosis Test | 
      Genetic | 
      Iron Overload Disorders | 
      General | 
      Hemochromatosis | 
      Various Labs | 
      FDA Approved | 
    
    
      | Microdeletion/Microduplication Testing | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Genetic Syndromes | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Cardiac Arrhythmia Panel | 
      Genetic | 
      Heart Rhythm Disorders | 
      Cardiac | 
      Arrhythmias | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Test for Gaucher Disease | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Gaucher's Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Cystic Fibrosis | 
      Carrier | 
      Cystic Fibrosis Carrier Status | 
      General | 
      Cystic Fibrosis | 
      Invitae | 
      FDA Approved | 
    
    
      | Non-Invasive Prenatal Testing | 
      Prenatal | 
      Fetal Chromosomal Abnormalities | 
      Pregnant | 
      Down Syndrome | 
      Natera | 
      FDA Approved | 
    
    
      | Genetic Counseling Consultation | 
      Counseling | 
      Pre/Post Test Counseling | 
      General | 
      Genetic Testing Education | 
      Various Providers | 
      Not Applicable | 
    
    
      | Testing for Lynch Syndrome | 
      Genetic | 
      Colorectal Cancer Risk | 
      Family | 
      Lynch Syndrome | 
      Invitae | 
      FDA Approved | 
    
    
      | Genetic Testing for Spinal Muscular Atrophy | 
      Carrier | 
      SMA Carrier Status | 
      General | 
      SMA | 
      Invitae | 
      FDA Approved | 
    
    
      | Fragile X Syndrome Testing | 
      Genetic | 
      Intellectual Disability | 
      General | 
      Fragile X Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Familial Mediterranean Fever Testing | 
      Genetic | 
      Auto Inflammatory Syndromes | 
      Ethnic Groups | 
      FMF | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Ellis-van Creveld Syndrome | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      Ellis-van Creveld Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Alzheimer's Genetic Risk Testing | 
      Genetic | 
      Alzheimer's Disease Risk | 
      General | 
      AD Risk Factors | 
      Various Labs | 
      FDA Approved | 
    
    
      | ENDURE Genetic Testing | 
      Diagnostic | 
      Childhood Genetic Disorders | 
      Pediatrics | 
      Various Disorders | 
      Invitae | 
      FDA Approved | 
    
    
      | Expanded Carrier Screening | 
      Carrier | 
      Broad Disease Carrier Status | 
      General | 
      Various Genetic Disorders | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for Neurofibromatosis | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      Neurofibromatosis | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Beta Thalassemia | 
      Genetic | 
      Blood Disorders | 
      General | 
      Thalassemia | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Test for Tay-Sachs Disease | 
      Carrier | 
      Tay-Sachs Carrier Status | 
      Ethnic Groups | 
      Tay-Sachs Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for LADD Syndrome | 
      Genetic | 
      Entodermal Sinus Tumor Risk | 
      General | 
      LADD Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | TP53 Testing for Li-Fraumeni Syndrome | 
      Genetic | 
      Cancer Risk Assessment | 
      Family | 
      Li-Fraumeni Syndrome | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Duchenne Muscular Dystrophy Testing | 
      Genetic | 
      Muscular Disorders | 
      General | 
      Duchenne Muscular Dystrophy | 
      Various Labs | 
      FDA Approved | 
    
    
      | Germline Genetic Testing | 
      Genetic | 
      Inherited Cancer Risks | 
      Family | 
      Various Cancers | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Hormonal Genomic Testing | 
      Pharmacogenomic | 
      Hormonal Response | 
      General | 
      Endocrine Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Medication Couple Genotyping | 
      Pharmacogenomic | 
      Drug Interaction Risks | 
      General | 
      Medication Efficacy | 
      Various Labs | 
      FDA Approved | 
    
    
      | Hereditary Prostate Cancer Gene Panel | 
      Genetic | 
      Prostate Cancer Risk | 
      Family | 
      Prostate Cancer | 
      Invitae | 
      FDA Approved | 
    
    
      | Genetic Testing for Alport Syndrome | 
      Genetic | 
      Kidney Disorders | 
      General | 
      Alport Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Family Tree Genetic Access Testing | 
      Ancestry | 
      Ancestry Information | 
      General | 
      Family History | 
      FamilySearch | 
      Not Required | 
    
    
      | Urothelial Carcinoma Risk Testing | 
      Genetic | 
      Bladder Cancer Risk | 
      General | 
      Urothelial Carcinoma | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Test for Osteogenesis Imperfecta | 
      Genetic | 
      Bone Disorders | 
      General | 
      Brittle Bone Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Comprehensive Metabolic Testing | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Various Metabolic Conditions | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Test for Methylenetetrahydrofolate Reductase | 
      Genetic | 
      Folic Acid Metabolism | 
      General | 
      MTHFR Variants | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Test for Netherton Syndrome | 
      Genetic | 
      Skin Disorders | 
      General | 
      Netherton Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Next Generation Sequencing for Mendelian Disorders | 
      Genetic | 
      Inherited Conditions | 
      General | 
      Mendelian Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Usher Syndrome | 
      Genetic | 
      Hearing and Vision Disorders | 
      General | 
      Usher Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for von Willebrand Disease | 
      Genetic | 
      Bleeding Disorders | 
      General | 
      Von Willebrand Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Progeria | 
      Genetic | 
      Aging Disorders | 
      General | 
      Progeria Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive Autism Spectrum Disorder Testing | 
      Genetic | 
      Developmental Disorders | 
      General | 
      ASD | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for HHT | 
      Genetic | 
      Vascular Disorders | 
      General | 
      Hereditary Hemorrhagic Telangiectasia | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for MCAD Deficiency | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Medium-Chain Acyl-CoA Dehydrogenase Deficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Panel for Inherited Cardiac Conditions | 
      Genetic | 
      Cardiomyopathy Risk | 
      Family | 
      Inherited Heart Disorders | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Kearns-Sayre Syndrome | 
      Genetic | 
      Mitochondrial Disorders | 
      General | 
      Kearns-Sayre Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Autosomal Dominant Polycystic Kidney Disease Testing | 
      Genetic | 
      Renal Disorders | 
      General | 
      ADPKD | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Mastocytosis | 
      Genetic | 
      Allergic Disorders | 
      General | 
      Mast Cell Disorders | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for PKU | 
      Genetic | 
      Metabolic Disorders | 
      Newborn | 
      Phenylketonuria | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Test for Birt-Hogg-Dubé Syndrome | 
      Genetic | 
      Cancer Risk | 
      General | 
      Birt-Hogg-Dubé Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive DNA Repair Gene Test | 
      Genetic | 
      Cancer Risk Assessment | 
      Family | 
      DNA Repair Disorders | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for Scurvy | 
      Genetic | 
      Vitamin Deficiency | 
      General | 
      Vitamin C Deficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Weissenbacher-Zweymüller Syndrome | 
      Genetic | 
      Rare Disorders | 
      General | 
      Weissenbacher-Zweymüller Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | APOE Genotyping for Alzheimer's Risk | 
      Genetic | 
      Risk Assessment | 
      General | 
      Alzheimer's Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Muir-Torre Syndrome | 
      Genetic | 
      Cancer Risk | 
      Family | 
      Muir-Torre Syndrome | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Neurofibromatosis Type 2 | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      Neurofibromatosis Type 2 | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hyperimmunoglobulin E Syndrome | 
      Genetic | 
      Immunodeficiency Disorders | 
      General | 
      Hyper-IgE Syndrome | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Retinoblastoma Genetic Testing | 
      Genetic | 
      Eye Cancer Risk | 
      Family | 
      Retinoblastoma | 
      Invitae | 
      FDA Approved | 
    
    
      | Genetic Panel for Myelodysplastic Syndromes | 
      Genetic | 
      Blood Disorders | 
      General | 
      Myelodysplastic Syndromes | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for Severe Combined Immunodeficiency | 
      Genetic | 
      Immunodeficiency Disorders | 
      Newborn | 
      SCID | 
      Various Labs | 
      FDA Approved | 
    
    
      | Test for Aicardi Syndrome | 
      Genetic | 
      Neurodevelopmental Disorders | 
      General | 
      Aicardi Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive Metabolism Panel | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Various Metabolic Conditions | 
      Invocation | 
      Research Use | 
    
    
      | Testing for THAP11-related Disorders | 
      Genetic | 
      Intellectual Disabilities | 
      General | 
      THAP11 Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Churg-Strauss Syndrome | 
      Genetic | 
      Systemic Vasculitis | 
      General | 
      Churg-Strauss Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | SAR1B Genetic Testing | 
      Genetic | 
      Lipid Disorders | 
      General | 
      SAR1B Deficiency | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for COACH Syndrome | 
      Genetic | 
      Mitochondrial Disorders | 
      General | 
      COACH Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Hereditary Breast and Ovarian Cancer Testing | 
      Genetic | 
      Cancer Risk | 
      Family | 
      BRCA1/2 Syndromes | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for Ornithine Transcarbamylase Deficiency | 
      Genetic | 
      Urea Cycle Disorders | 
      General | 
      OTC Deficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Iron Overload Genetic Testing | 
      Genetic | 
      Iron Metabolism Disorders | 
      General | 
      Hereditary Hemochromatosis | 
      GeneDx | 
      FDA Approved | 
    
    
      | Test for PODXL-related Disorders | 
      Genetic | 
      Kidney Disorders | 
      General | 
      PODXL Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Test for HUS | 
      Genetic | 
      Hemolytic Uremic Syndrome | 
      General | 
      HUS Risk | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for VACTERL Association | 
      Genetic | 
      Congenital Disorders | 
      General | 
      VACTERL Association | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Panel for Pancreatic Cancer Risk | 
      Genetic | 
      Pancreatic Cancer Assessment | 
      Family | 
      Pancreatic Cancer | 
      Invitae | 
      FDA Approved | 
    
    
      | Genetic Testing for Phelan-McDermid Syndrome | 
      Genetic | 
      Developmental Disorders | 
      General | 
      Phelan-McDermid Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive Gastrointestinal Genetic Testing | 
      Genetic | 
      GI Disorders | 
      General | 
      Various GI Conditions | 
      Ambry Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for RASopathies | 
      Genetic | 
      Genetic Syndromes | 
      General | 
      RASopathies | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Prader-Willi Syndrome | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Prader-Willi Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Ehlers-Danlos Syndrome | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Ehlers-Danlos Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genomic Medicine in Diabetes Testing | 
      Genetic | 
      Diabetes Risk | 
      General | 
      Diabetes Mellitus | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Aaron's Syndrome | 
      Genetic | 
      Developmental Disorders | 
      General | 
      Aaron's Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Coffin-Lowry Syndrome | 
      Genetic | 
      X-linked Mental Retardation | 
      General | 
      Coffin-Lowry Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Klinefelter Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Klinefelter Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Cleft Lip/Palate Syndromes | 
      Genetic | 
      Congenital Defects | 
      General | 
      Cleft Lip/Palate | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Noonan Syndrome | 
      Genetic | 
      Growth Disorders | 
      General | 
      Noonan Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Turner Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Turner Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Risk Assessment for Diabetes | 
      Genetic | 
      Diabetes Traits | 
      General | 
      Type 1 and Type 2 Diabetes | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Williams Syndrome | 
      Genetic | 
      Developmental Disorders | 
      General | 
      Williams Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for X-linked Agammaglobulinemia | 
      Genetic | 
      Immunodeficiency Disorders | 
      General | 
      XLA | 
      GeneDx | 
      FDA Approved | 
    
    
      | Fragile X Expanded Allele Testing | 
      Genetic | 
      Autism and Developmental Delays | 
      General | 
      Fragile X Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Usher Syndrome Type 1 | 
      Genetic | 
      Hearing and Vision Disorders | 
      General | 
      Usher Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Polycystic Ovary Syndrome | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      PCOS Genetic Test | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Cowden Syndrome | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      Cowden Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Familial Meningioma | 
      Genetic | 
      Brain Tumor Risk | 
      Family | 
      Meningioma | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Myhre Syndrome | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      Myhre Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hibernating Big Arm Syndrome | 
      Genetic | 
      Rare Disorders | 
      General | 
      Hibernating Big Arm Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Langerhans Cell Histiocytosis | 
      Genetic | 
      Hematologic Disorders | 
      General | 
      LCH | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Warfarin Sensitivity | 
      Pharmacogenomic | 
      Drug Metabolism | 
      General | 
      Warfarin Sensitivity | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Bardet-Biedl Syndrome | 
      Genetic | 
      Genetic Syndromes | 
      General | 
      Bardet-Biedl Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Profile for Fertility | 
      Genetic | 
      Fertility Assessment | 
      General | 
      Fertility Issues | 
      Various Labs | 
      FDA Approved | 
    
    
      | Comprehensive Skin Cancer Genetic Testing | 
      Genetic | 
      Skin Cancer Risk | 
      General | 
      Skin Cancer Risk Assessment | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Marfan Syndrome | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Marfan Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hypohidrotic Ectodermal Dysplasia | 
      Genetic | 
      Skin Disorders | 
      General | 
      Ectodermal Dysplasia | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for VHL Syndrome | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      von Hippel-Lindau | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Noonan syndrome 3 | 
      Genetic | 
      Growth and Development | 
      General | 
      Noonan Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Smith-Lemli-Opitz Syndrome | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      SLO Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for ABCD Syndrome | 
      Genetic | 
      Developmental Delays | 
      General | 
      ABCD Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | MGMT Methylation Testing | 
      Diagnostic | 
      Brain Tumor Assessment | 
      Oncology | 
      Gliomas | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Test for KIF1A-related Disorders | 
      Genetic | 
      Neurodevelopmental Disorders | 
      General | 
      KIF1A Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Crigler-Najjar Syndrome | 
      Genetic | 
      Liver Disorders | 
      General | 
      Crigler-Najjar Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Wolfram Syndrome | 
      Genetic | 
      Diabetes Insipidus | 
      General | 
      Wolfram Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Thrombocytopenia-absent radius syndrome | 
      Genetic | 
      Blood Disorders | 
      General | 
      TAR Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Test for Cacna1c-related Disorders | 
      Genetic | 
      Cardiovascular Disorders | 
      General | 
      Cacna1c Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Huntington Disease | 
      Genetic | 
      Neurodegenerative Disorders | 
      General | 
      Huntington's Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Sperm Analysis | 
      Genetic | 
      Fertility Assessment | 
      General | 
      Sperm Quality Assessment | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for A-Beta-Syndrome | 
      Genetic | 
      Rare Disorders | 
      General | 
      A-Beta Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Pankreas Divisum | 
      Genetic | 
      Pancreatic Disorders | 
      General | 
      Pankreas Divisum | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Gaucher Disease Type 3 | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Gaucher Type 3 | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Tuberous Sclerosis | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      Tuberous Sclerosis | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Connexin 26-related Hearing Loss | 
      Genetic | 
      Hearing Disorders | 
      General | 
      Connexin 26 | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Dandy-Walker Malformation | 
      Genetic | 
      Brain Development Disorders | 
      General | 
      Dandy-Walker Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Maple Syrup Urine Disease | 
      Genetic | 
      Metabolic Disorders | 
      Newborn | 
      MSUD | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Turner Syndrome Mix | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Turner Syndrome Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Genomics in Cancer Treatment | 
      Genetic | 
      Cancer Treatment | 
      Oncology | 
      Targeted Therapy | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Lynch Syndrome Variants | 
      Genetic | 
      Colorectal Cancer Risk | 
      Family | 
      Lynch Variants | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Testing for Congenital Hypothyroidism | 
      Genetic | 
      Endocrine Disorders | 
      Newborn | 
      Congenital Hypothyroidism | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Eosinophilic Esophagitis | 
      Genetic | 
      GI Disorders | 
      General | 
      Eosinophilic Esophagitis | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Pediatric Neurology | 
      Genetic | 
      Neurological Disorders | 
      Pediatrics | 
      Pediatric Neurological Disorders | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for XLID | 
      Genetic | 
      Mental Retardation | 
      General | 
      X-Linked ID | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Test for 22q11.2 Deletion Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      22q11.2 Deletion | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for CADASIL | 
      Genetic | 
      Vascular Disorders | 
      General | 
      CADASIL | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Frasier Syndrome | 
      Genetic | 
      Kidney Disorders | 
      General | 
      Frasier Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Waterhouse-Friderichsen Syndrome | 
      Genetic | 
      Adrenal Disorders | 
      General | 
      Waterhouse-Friderichsen | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Becton-Dickinson Syndrome | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Becton-Dickinson Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Dystonia | 
      Genetic | 
      Movement Disorders | 
      General | 
      Dystonia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Medullary Thyroid Carcinoma | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Medullary Thyroid Cancer | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for HNRNPH2-related Disorders | 
      Genetic | 
      Neurodevelopmental Disorders | 
      General | 
      HNRNPH2 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for LADD Syndrome | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      LADD Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Pallister-Killian Mosaic Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Pallister-Killian Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Marfan-related Disorders | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Marfan Spectrum Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Williams-Beuren Syndrome | 
      Genetic | 
      Developmental Disorders | 
      General | 
      Williams-Beuren Syndrome | 
      Genetic Health | 
      FDA Approved | 
    
    
      | Genetic Testing for Oligodontia | 
      Genetic | 
      Dental Disorders | 
      General | 
      Oligodontia Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Osteopetrosis | 
      Genetic | 
      Bone Density Disorders | 
      General | 
      Osteopetrosis | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Sotos Syndrome | 
      Genetic | 
      Growth Disorders | 
      General | 
      Sotos Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Neurodegenerative Conditions | 
      Genetic | 
      Neurodegeneration | 
      General | 
      Variety of Conditions | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for VATER Association | 
      Genetic | 
      Congenital Malformations | 
      General | 
      VATER Association | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Risk Testing for Drug Addiction | 
      Pharmacogenomic | 
      Substance Use Disorders | 
      General | 
      Addiction Profile | 
      Various Labs | 
      FDA Approved | 
    
    
      | Comprehensive Autism Genetic Testing | 
      Genetic | 
      Psychiatric Disorders | 
      General | 
      Autism Spectrum Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Argininosuccinate Lyase Deficiency | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Argininosuccinate Lyase Deficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Epilepsy | 
      Genetic | 
      Neurological Disorders | 
      General | 
      Epilepsy Types | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Sarcoidosis | 
      Genetic | 
      Inflammatory Disorders | 
      General | 
      Sarcoidosis Risks | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Barrett's Esophagus | 
      Genetic | 
      Esophageal Disorders | 
      General | 
      Barrett's Esophagus | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for CNS Disorders | 
      Genetic | 
      Central Nervous System Disorders | 
      General | 
      CNS Disorders | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Mitochondrial Encephalomyopathy | 
      Genetic | 
      Neuromuscular Disorders | 
      General | 
      Mitochondrial Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hypomagnesemia | 
      Genetic | 
      Electrolyte Disorders | 
      General | 
      Hypomagnesemia Risks | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Basal Cell Nevus Syndrome | 
      Genetic | 
      Skin Disorders | 
      General | 
      Basal Cell Nevus | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hyperparathyroidism | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Hyperparathyroidism | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Congenital Adrenal Hyperplasia | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Congenital Adrenal Hyperplasia | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Polygenic Risk Score | 
      Genetic | 
      Disease Risk Assessment | 
      General | 
      Polygenic Traits | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Multisystem Inflammatory Syndrome | 
      Genetic | 
      Inflammatory Disorders | 
      General | 
      MIS-C Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Albright Hereditary Osteodystrophy | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Albright Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Blue Rubber Bleb Nevus Syndrome | 
      Genetic | 
      Vascular Disorders | 
      General | 
      BRBNS | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Idiopathic Pulmonary Fibrosis | 
      Genetic | 
      Lung Disorders | 
      General | 
      IPF Risks | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for FAP | 
      Genetic | 
      Colon Cancer Risk | 
      General | 
      Familial Adenomatous Polyposis | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Testing for Borna Disease | 
      Genetic | 
      Viral Disorders | 
      General | 
      Borna Disease | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Fanconi Anemia | 
      Genetic | 
      Bone Marrow Disorders | 
      General | 
      Fanconi Anemia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Gitelman Syndrome | 
      Genetic | 
      Electrolyte Disorders | 
      General | 
      Gitelman Syndrome | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Sturge-Weber Syndrome | 
      Genetic | 
      Neurocutaneous Disorders | 
      General | 
      Sturge-Weber | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Bietti Crystalline Dystrophy | 
      Genetic | 
      Eye Disorders | 
      General | 
      Bietti Dystrophy | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Thalassemia Trait | 
      Carrier | 
      Blood Disorders | 
      General | 
      Thalassemia Trait | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Maple Syrup Urine Disease Carrier | 
      Carrier | 
      Metabolic Disorders | 
      General | 
      MSUD Carrier Status | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Multiple Endocrine Neoplasia | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      MEN Syndromes | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Glutaric Acidemia Type 1 | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Glutaric Acidemia | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for IDH1/IDH2 Mutations | 
      Genetic | 
      Tumor Genetics | 
      General | 
      IDH-mutant Tumors | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for G6PD Deficiency | 
      Genetic | 
      Blood Disorders | 
      General | 
      G6PD Deficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for KAT6A-related Disorders | 
      Genetic | 
      Neurodevelopmental Disorders | 
      General | 
      KAT6A Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Risk Testing for Obesity | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Weight Management | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Impaired Glucose Tolerance | 
      Genetic | 
      Diabetes Risks | 
      General | 
      Metabolic Assessment | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetics in Pregnancy Testing | 
      Genetic | 
      Prenatal Assessment | 
      Pregnant | 
      Family Planning | 
      Various Labs | 
      FDA Approved | 
    
    
      | Comprehensive Genetic Test for Skin Cancer | 
      Genetic | 
      Cancer Risk Assessment | 
      General | 
      Skin Cancer Markers | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Betel Nut-related Disorders | 
      Genetic | 
      Oral Disorders | 
      General | 
      Tobacco and Betel Nut Use | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Congenital Thrombocytopenia | 
      Genetic | 
      Blood Disorders | 
      General | 
      Congenital Thrombocytopenia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Dystrophic Epidermolysis Bullosa | 
      Genetic | 
      Skin Disorders | 
      General | 
      Dystrophic EB | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Klinefelter Syndrome Carrier Status | 
      Carrier | 
      Chromosomal Disorders | 
      General | 
      Klinefelter Traits | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Achondrogenesis | 
      Genetic | 
      Skeletal Dysplasia | 
      General | 
      Achondrogenesis | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Temporal Lobe Epilepsy | 
      Genetic | 
      Neuromuscular Disorders | 
      General | 
      Temporal Epilepsy Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive Cardiomyopathy Genetic Panel | 
      Genetic | 
      Cardiac Disorders | 
      General | 
      Cardiomyopathy | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Ehlers-Danlos Syndrome Hypermobile Type | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Hypermobile EDS | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for PAX6-related Disorders | 
      Genetic | 
      Eye Disorders | 
      General | 
      PAX6 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for CXL Syndrome | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      CXL Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Pheochromocytoma | 
      Genetic | 
      Tumor Risk Assessment | 
      Family | 
      Pheochromocytoma | 
      Invitae | 
      FDA Approved | 
    
    
      | Testing for Cohen Syndrome | 
      Genetic | 
      Neurodevelopmental Disorders | 
      General | 
      Cohen Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Comprehensive Genetic Testing for Thyroid Disorders | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Thyroid Conditions | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Pathogenic FAP Variants | 
      Genetic | 
      Cancer Risk | 
      Family | 
      Familial Adenomatous Polyposis | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Nonsense-Mediated Decay Disorders | 
      Genetic | 
      Genetic Disorders | 
      General | 
      Nonsense-Mediated Decay | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Galactosemia | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Galactosemia Carrier Status | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Mucopolysaccharidosis IX | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      MPS IX | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for cystic fibrosis carriers | 
      Carrier | 
      Lung Disease | 
      General | 
      Cystic Fibrosis | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Hereditary Nonpolyposis Colorectal Cancer | 
      Genetic | 
      Cancer Risk Assessment | 
      Family | 
      Lynch Syndrome | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Genetic Testing for Type 1 Diabetes Risk | 
      Genetic | 
      Diabetes Risk | 
      General | 
      Type 1 Diabetes Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Digan Syndrome | 
      Genetic | 
      Developmental Disorders | 
      General | 
      Digan Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Lichtenstein's Disease | 
      Genetic | 
      Skin Disorders | 
      General | 
      Lichtenstein's Disease | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Hypertrophic Cardiomyopathy | 
      Genetic | 
      Cardiac Disorders | 
      Family | 
      HCM Risk Assessment | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Renal Tubular Acidosis | 
      Genetic | 
      Kidney Disorders | 
      General | 
      RTA Type | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Retinitis Pigmentosa | 
      Genetic | 
      Eye Disorders | 
      General | 
      Retinitis Pigmentosa | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Ocular Albinism | 
      Genetic | 
      Eye Disorders | 
      General | 
      Ocular Albinism | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Prostate Cancer Risk | 
      Genetic | 
      Cancer Risk Assessment | 
      Family | 
      Prostate Cancer | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Testing for Becker Muscular Dystrophy | 
      Genetic | 
      Muscular Disorders | 
      General | 
      Becker's Dystrophy | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Myotonic Dystrophy Type 2 | 
      Genetic | 
      Muscular Disorders | 
      General | 
      Myotonic Dystrophy | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for KCNQ2-related disorders | 
      Genetic | 
      Neurological Disorders | 
      General | 
      KCNQ2 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Spinocerebellar Ataxia | 
      Genetic | 
      Movement Disorders | 
      General | 
      Spinocerebellar Ataxia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Non-Syndromic Hearing Loss | 
      Genetic | 
      Hearing Disorders | 
      General | 
      Hearing Loss Genes | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Semi-Dominant Ehlers-Danlos Syndrome | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Semi-Dominant EDS | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Marfan Syndrome | 
      Genetic | 
      Connective Tissue Disorders | 
      General | 
      Marfan Traits | 
      Myriad Genetics | 
      FDA Approved | 
    
    
      | Testing for Malignant Hyperthermia | 
      Genetic | 
      Anesthetic Complications | 
      General | 
      Malignant Hyperthermia Risk | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Schimke Immuno-osseous Dysplasia | 
      Genetic | 
      Immune Disorders | 
      General | 
      Schimke Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Rheumatoid Factor | 
      Genetic | 
      Autoimmune Disorders | 
      General | 
      Rheumatoid Arthritis | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Neurodegenerative Diseases Testing | 
      Genetic | 
      Neurodegenerative Disorders | 
      General | 
      Dementia Risk Assessments | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for PCH | 
      Genetic | 
      Cerebellar Ataxia | 
      General | 
      PCH Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Pituitary Disorders | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Pituitary Conditions | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Kearns-Sayre Syndrome | 
      Genetic | 
      Mitochondrial Disorders | 
      General | 
      Kearns-Sayre Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Ca2+ Channelopathies | 
      Genetic | 
      Neuromuscular Disorders | 
      General | 
      Ca2+ Channel Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Fetal Alcohol Spectrum Disorders | 
      Genetic | 
      Developmental Delays | 
      General | 
      FASD Risk Assessment | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Chiari Malformation | 
      Genetic | 
      Neurological Disorders | 
      General | 
      Chiari Malformation | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Holoprosencephaly | 
      Genetic | 
      Brain Development Disorders | 
      General | 
      Holoprosencephaly Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Phosphomannomutase 2 Deficiency | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      PMM2 Deficiency | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Tetrahydrobiopterin Deficiency | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      PKU Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for SLC16A12-related disorders | 
      Genetic | 
      Kidney Disorders | 
      General | 
      SLC16A12 Deficiency | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for TMED10 | 
      Genetic | 
      Neuromuscular Disorders | 
      General | 
      TMED10 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Urethral Atresia | 
      Genetic | 
      Congenital Defects | 
      General | 
      Urethral Atresia Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for X-Linked SCID | 
      Genetic | 
      Immunodeficiency Disorders | 
      General | 
      X-Linked Severe Combined Immunodeficiency | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for AAAS-associated Disorders | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      AAAS Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Pulmonary Alveolar Proteinosis | 
      Genetic | 
      Lung Disorders | 
      General | 
      Pulmonary Alveolar Proteinosis | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Dipeptidyl Peptidase-4 Deficiency | 
      Genetic | 
      Glyco-Disorders | 
      General | 
      DPP-IV Deficiency | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for ALL | 
      Genetic | 
      Blood Disorders | 
      General | 
      Acute Lymphoblastic Leukemia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Cystic Fibrosis Modifier Genes | 
      Genetic | 
      Lung Disorders | 
      General | 
      CF Modifiers | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Rabson-Mendenhall Syndrome | 
      Genetic | 
      Endocrine Disorders | 
      General | 
      Rabson-Mendenhall Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Severe Scissor-Gait Dystonia | 
      Genetic | 
      Neuromuscular Disorders | 
      General | 
      Scissor-Gait | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Efficacy of Anti-Psychotic Drugs | 
      Pharmacogenomic | 
      Psychiatric Disorders | 
      General | 
      Anti-Psychotic Response | 
      Various Labs | 
      FDA Approved | 
    
    
      | Genetic Testing for Y-chromosome microdeletions | 
      Genetic | 
      Infertility | 
      General | 
      Male Infertility | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Cystinosis Carrier Status | 
      Carrier | 
      Metabolic Disorders | 
      General | 
      Cystinosis | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Alport Syndrome Carrier Status | 
      Carrier | 
      Kidney Disorders | 
      General | 
      Alport Carrier Risk | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Hearing Loss due to Connexin 30 | 
      Genetic | 
      Hearing Disorders | 
      General | 
      Connexin 30 | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for SAA-related Disorders | 
      Genetic | 
      Immuno-inflammatory Disorders | 
      General | 
      SAA Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Agammaglobulinemia | 
      Genetic | 
      Immunodeficiency Disorders | 
      General | 
      XLA Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for MCL1 Associated Disorders | 
      Genetic | 
      Cancer Risk | 
      General | 
      MCL1 Associated Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for AKU | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      Alcaptonuria | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Brachyplasia | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      Brachyplasia | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for WAGR Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      WAGR Syndrome | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Spondyloepiphyseal Dysplasia | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      SED Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Examining Mycobacterium leprae strains | 
      Genetic | 
      Infectious Diseases | 
      General | 
      Leprosy Genetics | 
      Various Labs | 
      FDA Approved | 
    
    
      | Testing for Wiskott-Aldrich Syndrome | 
      Genetic | 
      Immunodeficiency Disorders | 
      General | 
      WAS Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for GJB2-Related Hearing Loss | 
      Genetic | 
      Hearing Disorders | 
      General | 
      GJB2 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for MCD | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      MCD Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for RET Pathway Disorders | 
      Genetic | 
      Tumor Syndromes | 
      General | 
      RET Pathway Tumors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Secondary Male Infertility | 
      Genetic | 
      Infertility | 
      General | 
      Infertility Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Thymoma Genotyping | 
      Genetic | 
      Tumor Markers | 
      General | 
      Thymoma Genetic Assessment | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for LCH | 
      Genetic | 
      Hematologic Disorders | 
      General | 
      LCH Genetic Profile | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Turner Syndrome Associated Variants | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      Turner Traits | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Erythropoietic Protoporphyria | 
      Genetic | 
      Skin Disorders | 
      General | 
      EPP Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Rare Tumor Panel | 
      Genetic | 
      Tumor Risk | 
      General | 
      Rare Tumors Risk Assessment | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for ATAXIA | 
      Genetic | 
      Neuropathy Disorders | 
      General | 
      Ataxia Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for MUD | 
      Genetic | 
      Hematologic Disorders | 
      General | 
      MUD Genetic Profile | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Infantile-onset Pompe Disease | 
      Genetic | 
      Muscle Disorders | 
      General | 
      Pompe Disease Risk | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for NOS3 | 
      Genetic | 
      Cardiac Disorders | 
      General | 
      NOS3 Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for Familial Hypercholesterolemia | 
      Genetic | 
      Lipid Disorders | 
      General | 
      Lipid Metabolism Issues | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Test for Sarcopenia-related Disorders | 
      Genetic | 
      Muscle Weakness Disorders | 
      General | 
      Sarcopenia Risk Assessment | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for TTS Syndrome | 
      Genetic | 
      Skeletal Disorders | 
      General | 
      TTS Risks | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for EDD | 
      Genetic | 
      Genetic Predisposition Disorders | 
      General | 
      EDD Risk Factors | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for TSEN54 Mutation-induced Disorders | 
      Genetic | 
      Neurodegenerative Disorders | 
      General | 
      TSEN54 Risks | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for X-linked Myotubular Myopathy | 
      Genetic | 
      Muscle Disorders | 
      General | 
      Myotubular Myopathy | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for WI38-related Disorders | 
      Genetic | 
      Aging Disorders | 
      General | 
      WI38 Risks | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for Anemia Risk Factors | 
      Genetic | 
      Blood Disorders | 
      General | 
      Anemia Variants | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for ENPP1 Deficiency | 
      Genetic | 
      Metabolic Disorders | 
      General | 
      ENPP1 Disorders | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Testing for EPI | 
      Genetic | 
      Pancreatic Disorders | 
      General | 
      Exocrine Pancreatic Insufficiency | 
      GeneDx | 
      FDA Approved | 
    
    
      | Testing for 15q Duplication Syndrome | 
      Genetic | 
      Chromosomal Disorders | 
      General | 
      15q Duplication | 
      GeneDx | 
      FDA Approved | 
    
    
      | Genetic Risk Testing for Polygenic Obesity | 
      Genetic | 
      Obesity Risk | 
      General | 
      Polygenic Obesity | 
      GeneDx | 
      FDA Approved |