UAB Medical Genomics Laboratory

UAB Medical Genomics Laboratory, MGL
UAB Medicine (UAB)
Department: Hospital Labs
720 20th Street South Suite 330
Birmingham, Alabama, United States 35294-0024
Phone: 205-934-5562
Fax: 205-996-2929
Email: medgenomics@uabmc.edu
Online Contact: https://www.uab.edu/medicine/genetics/medical-genomics-laboratory/contact-us
Website: https://www.uab.edu/medicine/genetics/medical-genomics-laboratory

Submissions in ClinVar
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GTR Lab ID: 221768, Last updated:2024-07-22
Annual Review past due read more

Personnel

Director: Yunjia Chen, PhD, FACMG, Lab Director
Email: yunjiachen@uabmc.edu
Director: Yulong Fu, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
Phone: 205-934-5562
Fax: 205-996-2929
Email: yulongfu@uabmc.edu
Ryan Lauterbach, BS, Genetic Counselor Assistant
Phone: 205-934-7387
Fax: 205-966-2929
Email: rlauterbach@uabmc.edu
Contact note: medgenomics@uabmc.edu
Victoria Moy, MS, Genetic Counselor
Phone: 205-934-5528
Fax: 205-996-2929
Email: vmoy@uabmc.edu
Amber Richardson, BSc, MLS(ASCP), Administrator
Phone: 205-934-5562
Email: aprichardson@uabmc.edu
Brandon Shaw, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
Phone: 205-934-1520
Fax: 205-966-2929
Email: brandonshaw@uabmc.edu
Contact note: medgenomics@uabmc.edu
Ying Wang, MS, MBA, Laboratory Manager
Phone: 205-934-9889
Fax: 205-996-2929
Email: yingw@uab.edu
Contact note: 205-934-5562

Conditions and tests

37 conditions/phenotypes with 23 tests
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Atypical teratoid rhabdoid tumor2 tests
Bannayan-Riley-Ruvalcaba syndrome1 test
Cafe au lait spots, multiple1 test
Capillary malformation-arteriovenous malformation syndrome1 test
Cardiofaciocutaneous syndrome 12 tests
Costello syndrome3 tests
Familial meningioma1 test
Fragile X syndrome1 test
Juvenile myelomonocytic leukemia2 tests
Legius syndrome5 tests
Macrocephaly-autism syndrome1 test
Malignant rhabdoid tumor, somatic2 tests
Medium-chain acyl-coenzyme A dehydrogenase deficiency1 test
Meningioma1 test
Neurofibromatosis, familial spinal3 tests
Neurofibromatosis, type 18 tests
Neurofibromatosis, type 27 tests
Neurofibromatosis-Noonan syndrome2 tests
Noonan syndrome2 tests
Noonan syndrome with multiple lentigines2 tests
Noonan syndrome-like disorder with loose anagen hair2 tests
Parkes Weber syndrome1 test
Proteus syndrome1 test
Proteus-like syndrome1 test
PTEN hamartoma tumor syndrome1 test
Rhabdoid tumor1 test
Rhabdoid tumor predisposition syndrome 12 tests
Rhabdoid tumor predisposition syndrome 22 tests
Schwannomatosis1 test
Schwannomatosis 15 tests
Schwannomatosis 21 test
SCHWANNOMATOSIS, SOMATIC1 test
Schwannomatosis-1, susceptibility to1 test
Tuberous sclerosis 11 test
Tuberous sclerosis 21 test
Tuberous sclerosis syndrome1 test
Von Hippel-Lindau syndrome1 test

List of services

Insurance billing
Insurance preverification
Biopsy-based/mosaicism analysis
Clinical Testing/Confirmation of Mutations Identified Previously: Order Code: KT2
Custom Deletion/Duplication Testing: Order Code: KT2
Custom Sequence Analysis: Order Code: KT2
Carrier testing: Order Code: KT2 or KT2-NG
Prenatal testing: Order Code: PT2
Maternal cell contamination study (MCC): Order Code: PT2

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: 01D0301478, Expiration date: 2025-11-28
CAP, Number: 1544506, Expiration date: 2025-02-05

Licenses

CA - California Department of Public Health CDPH, Number: CDS-90006628, Expiration date: 2025-04-27
MD - Maryland Department of Health and Mental Hygiene DHMH, Number: 1517
PA - Pennsylvania Department of Health PADOH, Number: 33933, Expiration date: 2024-08-15

Participation in external programs

Standardization programs

Locus-specific Databases
Mutation-specific Databases

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