GTR Home > Laboratories > Department of Clinical Genetics

Department of Clinical Genetics

GTR Lab ID: 320438, Last updated:2017-10-24


Conditions and tests

  • Breast-ovarian cancer, familial 11 test
  • Breast-ovarian cancer, familial 21 test
  • Cutaneous malignant melanoma 21 test
  • Hereditary angioedema type 11 test
  • Hereditary angioneurotic edema1 test
  • Hereditary C1 esterase inhibitor deficiency - dysfunctional factor1 test
  • Hereditary diffuse gastric cancer1 test
  • Hereditary pancreatitis1 test
  • Lynch syndrome1 test
  • Lynch syndrome I1 test
  • Lynch syndrome II1 test
  • Multiple endocrine neoplasia, type 21 test
  • Turcot syndrome1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Custom Deletion/Duplication Testing
  • Genetic counseling
  • Mutation Confirmation
  • Result interpretation

List of certifications/licenses


  • EMQN, Number: 0400, Expiration date: 2014-05-01

Participation in external programs

Standardization programs

  • Mutation-specific Databases
  • Other

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.

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