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 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 12 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 11 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 12 |
|
Genesys Diagnostics Genesys Diagnostics, Inc. United States | 1 | 20 |
|
F2 Gene Factor II deficiency NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
F2 Gene Thrombophilia due to thrombin defect NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
F2 Gene Dysprothrombinemia NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Gravity Pharmacogenetics Comprehensive Profile Gravity Diagnostics United States | 86 | 17 |
|
Genetic study of pharmacogenetics HeartGenetics, Genetics and Biotechnology, SA Portugal | 1 | 26 |
|
F2 Gene, Full Gene Next-Generation Sequencing Mayo Clinic Laboratories Mayo Clinic United States | 1 | 1 |
|
Genetic Study of Hereditary Thrombophilia (11 genes, 15 variants) HeartGenetics, Genetics and Biotechnology, SA Portugal | 1 | 11 |
|
Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
|
Invitae United States | 24 | 8 |
|
Eugenomic S.L. Spain | 1 | 16 |
|
Eugenomic S.L. Spain | 1 | 21 |
|
F2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 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 | 669 | 688 |
|
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.