- Unknonw type - GTR - NCBI

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Unknonw type

offered by

GTR Test Accession:

Last updated in GTR:

At a Glance

Conditions (20):

Primary familial polycythemia due to EPO receptor mutation; Acquired polycythemia vera; Acute myeloid leukemia; ...

Genes (15):

ASXL1 (20q11.21), CALR (19p13.13), CBL (11q23.3), CSF3R (1p34.3), DNMT3A (2p23.3), ...

Conditions

Total conditions: 20

Condition/Phenotype	Identifier

Methodology

Total methods: 0

Method Category

Test method

Instrument *

* Instrument: Not provided

Technical Information

Recommended fields not provided:

Test Confirmation

Additional Information

Reviews:

PubMed Clinical Queries

Reviews in PubMed

Clinical resources:

Clinicaltrials.gov

Molecular resources:

View EPOR variations in ClinVar

View JAK2 variations in ClinVar

View SH2B3 variations in ClinVar

Coriell Institute for Medical Research

Practice guidelines:

EuroGenetest, 2012

Consumer resources:

Genetic Alliance

NCATS Office of Rare Diseases Research (GARD)

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in 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.