Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
SmartMeds+ Pharmacogenomic Testing By Innovative GX Health Innovative Genomics InnovativeGx Health United States | 1 | 67 |
|
RPRD Diagnostics, LLC United States | 107 | 69 |
|
Genomind Pharmacogenetic Report Genomind, Inc. Genomind, Inc United States | 14 | 27 |
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Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 12 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 11 |
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Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 12 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 20 |
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Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 10 |
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MTHFR Gene Homocystinuria NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Tempus Labs, Inc. United States | 2 | 647 |
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Genetic Study of Hereditary Thrombophilia (11 genes, 15 variants) HeartGenetics, Genetics and Biotechnology, SA Portugal | 1 | 11 |
|
Centogene AG - the Rare Disease Company Germany | 316 | 314 |
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MTHFR - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 734 | 744 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Centogene AG - the Rare Disease Company Germany | 669 | 688 |
|
Centogene AG - the Rare Disease Company Germany | 829 | 848 |
|
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
|
Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States | 346 | 160 |
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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.