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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

Riboflavin deficiency, 615026, Autosomal dominant; RBFVD (Maternal riboflavin deficiency) (SLC52A1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Riboflavin deficiency, 615026, Autosomal dominant; RBFVD (Maternal riboflavin deficiency) (SLC52A1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Disorders of Fatty Acid Oxidation (FAOD) Panel

PreventionGenetics, part of Exact Sciences
United States
3232
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Comprehensive Neuropathies Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
223106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Elevated C4 and C5 (Multiple Acyl-CoA Dehydrogenase deficiency) Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
99
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC52A1 Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 7 of 7

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.