U.S. flag

An official website of the United States government

Filters

reset all

Other countries

Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 2, Mutations (c.232 G>A,c.232 G>C) SDHAF2/PGL2 Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Comprehensive Hereditary Cancer Panel

Baylor Genetics
United States
13261
  • E Sequence analysis of select exons

Hereditary Endocrine Cancer Panel

Baylor Genetics
United States
5115
  • E Sequence analysis of select exons

Hereditary Paraganglioma/Pheochromocytoma Panel

Baylor Genetics
United States
219
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Renal Cancer Panel

Baylor Genetics
United States
4113
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Paraganglioma-pheochromocytoma 2 (PGL2) syndrome , Hereditary: SDHAF2 gene mutation analysis (c.232G>A, c.232G>C)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • E Sequence analysis of select exons

Results: 1 to 6 of 6

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.