Seattle Children's Hospital Genetics Laboratories

Personnel

Director: Cate Paschal, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
Director: James Bennett, PhD, MD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Associate Director
Director: Nya Nelson, PhD, MD, Lab Associate Director
Director: Anica Wandler, PhD, Lab Associate Director
Susan Schowalter, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
Phone: 206-987-5400
Email: labgc@seattlechildrens.org
Darci Sternen, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
Phone: 206-987-5400
Email: LabGC@seattlechildrens.org
Shelia Stumvoll, Administrator
Phone: 206-987-5066
Email: Sheila.Stumvoll@seattlechildrens.org

Conditions and tests

50 conditions/phenotypes with 3 tests
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Abnormality of the lymphatic system3 tests
Arteriovenous malformation2 tests
Basal ganglia calcification, idiopathic, 42 tests
Capillary malformation2 tests
Capillary malformation-arteriovenous malformation 13 tests
Capillary malformation-arteriovenous malformation 23 tests
Cardiofaciocutaneous syndrome 23 tests
Cardiofaciocutaneous syndrome 33 tests
Cerebral cavernous malformation2 tests
Cerebral cavernous malformation 22 tests
Cerebral cavernous malformation 32 tests
CLAPO syndrome3 tests
CLOVES syndrome3 tests
Costello syndrome3 tests
Cowden syndrome 12 tests
D-2-hydroxyglutaric aciduria 22 tests
Deafness-lymphedema-leukemia syndrome3 tests
Distichiasis-lymphedema syndrome3 tests
Encephalocraniocutaneous lipomatosis2 tests
Epidermal nevus3 tests
Glioma susceptibility 12 tests
Glomuvenous malformation2 tests
Hemangioma2 tests
Hennekam lymphangiectasia-lymphedema syndrome 13 tests
Hennekam lymphangiectasia-lymphedema syndrome 23 tests
Hereditary lymphedema type I3 tests
Hypotrichosis-lymphedema-telangiectasia syndrome3 tests
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome3 tests
Juvenile nasopharyngeal angiofibroma2 tests
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome2 tests
Large congenital melanocytic nevus3 tests
Lymphatic malformation2 tests
Lymphatic malformation 103 tests
Lymphatic malformation 123 tests
Lymphatic malformation 33 tests
Lymphatic malformation 43 tests
Lymphedema3 tests
Lymphedema-posterior choanal atresia syndrome3 tests
Megalencephaly-capillary malformation-polymicrogyria syndrome3 tests
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability3 tests
Multiple cutaneous and mucosal venous malformations2 tests
Myofibromatosis, infantile, 12 tests
Neurocutaneous melanocytosis3 tests
Noonan syndrome 33 tests
Noonan syndrome 63 tests
Primary intraosseous venous malformation2 tests
Telangiectasia, hereditary hemorrhagic, type 12 tests
Telangiectasia, hereditary hemorrhagic, type 22 tests
Telangiectasia, hereditary hemorrhagic, type 52 tests
Toriello-Lacassie-Droste syndrome3 tests

List of services

This lab has no services.

List of certifications/licenses

Certifications

CLIAHelpCertification number assigned by the Clinical Laboratory Improvement Amendments (CLIA) program to the laboratory director. Minimal field for US labs offering clinical tests. Optional field for international labs or US labs performing research tests. If pending renewal or record has not been updated, the expiration date may be in the past., Number: 50D0631879, Expiration date: 2025-06-30
CLIA, Number: 50D0931679, Expiration date: 2025-06-30
CAP, Number: 2463801, Expiration date: 2025-06-01

Participation in external programs

Data exchange Programs

Mutation-specific Databases

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.