Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
cfDNA KRAS 12, 13, 61, 146 Blood Mayo Clinic Laboratories Mayo Clinic United States | 1 | 1 |
|
KRAS Somatic Mutation Analysis, Tumor Mayo Clinic Laboratories Mayo Clinic United States | 2 | 1 |
|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Centogene AG - the Rare Disease Company Germany | 58 | 28 |
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Centogene AG - the Rare Disease Company Germany | 67 | 33 |
|
Centogene AG - the Rare Disease Company Germany | 114 | 68 |
|
Centogene AG - the Rare Disease Company Germany | 156 | 107 |
|
Centogene AG - the Rare Disease Company Germany | 218 | 135 |
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Centogene AG - the Rare Disease Company Germany | 74 | 34 |
|
DCC - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 12 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 5 | 1 |
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AKT1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
|
EP300 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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FGFR3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 14 | 1 |
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FLCN - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
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MLH3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
NRAS - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 8 | 1 |
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PIK3CA - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 14 | 1 |
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TP53 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 12 | 1 |
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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.