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Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

[Skin/hair/eye pigmentation 9, brown/nonbrown eyes], 611742 (ASIP 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

[Skin/hair/eye pigmentation 9, dark/light hair], 611742 (ASIP 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

Charcot-Marie-Tooth disease type 2A2 (CMT2A2, sequence analysis of MFN2 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

ASIP Single Gene

Fulgent Genetics
United States
11
  • 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 5 of 5

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.