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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Genomind Pharmacogenetic Report Genomind, Inc. Genomind, Inc United States | 14 | 27 |
|
ANK3 Gene Mental retardation, autosomal recessive type 37 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Health in Code Spain | 1 | 218 |
|
Brugada syndrome / J wave syndrome Health in Code Spain | 1 | 25 |
|
Cardiovascular Diseases_General Panel Health in Code Spain | 1 | 380 |
|
Ventricular arrhythmia and sudden death without structural heart disease Health in Code Spain | 1 | 77 |
|
Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease Health in Code Spain | 1 | 53 |
|
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease Health in Code Spain | 1 | 141 |
|
Health in Code Spain | 1 | 23 |
|
Inherited Cardiovascular Diseases and Sudden Death Panel Health in Code Spain | 1 | 213 |
|
Health in Code Spain | 1 | 23 |
|
ANK3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 734 | 744 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
|
Genetic Services Laboratory University of Chicago United States | 6 | 216 |
|
Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.