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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Natera, Inc. United States | 265 | 274 |
|
Corticosterone Methyloxidase Deficiency (CYP11B2 Single Gene Test) Fulgent Genetics United States | 2 | 1 |
|
Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States | 716 | 335 |
|
Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States | 636 | 298 |
|
Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States | 661 | 306 |
|
Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States | 690 | 326 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Congenital Hypoaldosteronism due to CMO I Deficiency, Sequencing CYP11B2 Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
FAMILIAL HYPERRENINEMIC HYPOALDOSTERONISM TYPE 1 Laboratorio de Genetica Clinica SL Spain | 2 | 1 |
|
Familial hyperreninemic hypoaldosteronism type 1 Bioarray Spain | 1 | 1 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Corticosterone methyloxidase type 1 deficiency Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany | 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.