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Results: 1 to 20 of 25

Tests names and labsConditionsGenes and analytesMethods

Hemochromatosis type 3

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperferritinemia Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
1515
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis via the TFR2 Gene

PreventionGenetics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Hemochromatosis NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
77
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TFR2. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

TFR2. Detection of the mutations p.Arg30ProfsX31, p.Met172Lys, p.Tyr250X and p.Ala621_Gln624del by sequencing

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

Adult Hereditary Hemochromatosis type 3

Diagnostics in Iron Metabolism Diseasess (DIRON) Josep Carreras Leukaemia Research Institute
Spain
11
  • C Sequence analysis of the entire coding region

TFR2 Gene Sequencing

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • C Sequence analysis of the entire coding region

Hemochromatosis NGS Panel

DDC Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
157
  • C Sequence analysis of the entire coding region

CarrierMap

Recombine
United States
299297
  • T Targeted variant analysis

Hemochromatosis type 3

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

TFR2 Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Genetic disorders with abnormal pigmentation Panel

CeGaT GmbH
Germany
2932
  • C Sequence analysis of the entire coding region

Hemochromatosis type 3, Hereditary: TFR2 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Hemochromatosis type 3, Hereditary: TFR2 gene mutation screening

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • T Targeted variant analysis

TFR2

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Hemochromatosis Panel

Invitae
United States
65
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemochromatosis

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Hemochromatosis

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Hemochromatosis type 3, Hereditary: TFR2 gene, Y250X mutation

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • T Targeted variant analysis

Results: 1 to 20 of 25

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.