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 |