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GTR Home > Laboratories > Northwest Clinical Genomics Laboratory

Northwest Clinical Genomics Laboratory

GTR Lab ID: 505538, Last updated:2024-03-28

Personnel

  • Director: Christina Lockwood, PhD, ABMGG Board Certified, FACMG, Diplomate of the American Board of, Lab Director
    Phone: 206-543-5464
    Fax: 206-616-1899
    Email: tinalock@uw.edu
  • Dru Leistritz, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
    Phone: 206-543-5464
    Fax: 206-616-1899
    Email: dru2@uw.edu

Conditions and tests

  • 3-Methylglutaconic aciduria type 21 test
  • Arrhythmogenic right ventricular cardiomyopathy2 tests
  • Arrhythmogenic right ventricular dysplasia 21 test
  • Arrhythmogenic right ventricular dysplasia 51 test
  • Arrhythmogenic right ventricular dysplasia 91 test
  • Atrial fibrillation, familial, 122 tests
  • Atrial septal defect 51 test
  • Atrial septal defect 71 test
  • Autosomal recessive limb-girdle muscular dystrophy1 test
  • Brugada syndrome2 tests
  • Cardio-facio-cutaneous syndrome1 test
  • Catecholaminergic polymorphic ventricular tachycardia1 test
  • Catecholaminergic polymorphic ventricular tachycardia 11 test
  • Catecholaminergic polymorphic ventricular tachycardia 21 test
  • Catecholaminergic polymorphic ventricular tachycardia 51 test
  • Centronuclear myopathy1 test
  • Congenital long QT syndrome1 test
  • Costello syndrome1 test
  • Danon disease1 test
  • Desmin-related myofibrillar myopathy1 test
  • Dilated cardiomyopathy 1A1 test
  • Dilated cardiomyopathy 1C1 test
  • Dilated cardiomyopathy 1D1 test
  • Dilated cardiomyopathy 1DD1 test
  • Dilated cardiomyopathy 1EE1 test
  • Dilated cardiomyopathy 1G1 test
  • Dilated cardiomyopathy 1L1 test
  • Dilated cardiomyopathy 1P1 test
  • Distal myopathy, Tateyama type1 test
  • Fabry disease, cardiac variant1 test
  • Familial atrial fibrillation1 test
  • Familial restrictive cardiomyopathy1 test
  • Glycogen storage disease II, adult form1 test
  • Hereditary amyloidosis1 test
  • Hereditary disease2 tests
  • Hypertrichotic osteochondrodysplasia Cantu type1 test
  • Hypertrophic cardiomyopathy2 tests
  • Hypertrophic cardiomyopathy 21 test
  • Hypertrophic cardiomyopathy 61 test
  • KCNQ1-related acquired long QT syndrome1 test
  • Lethal acantholytic epidermolysis bullosa1 test
  • Long QT syndrome 1/2, digenic1 test
  • Long QT syndrome 101 test
  • Long QT syndrome 121 test
  • Long QT syndrome 131 test
  • Long QT syndrome 141 test
  • Long QT syndrome 151 test
  • Long QT syndrome 21 test
  • Long QT syndrome 31 test
  • Long QT syndrome 41 test
  • Long QT syndrome 51 test
  • Long QT syndrome 61 test
  • Long QT syndrome 92 tests
  • Myofibrillar myopathy1 test
  • Myofibrillar myopathy 61 test
  • Myosin storage myopathy1 test
  • Noonan syndrome1 test
  • Noonan syndrome with multiple lentigines1 test
  • Primary dilated cardiomyopathy1 test
  • Primary familial hypertrophic cardiomyopathy1 test
  • Progressive familial heart block type IB1 test
  • Qualitative or quantitative defects of dystrophin1 test
  • Sinoatrial node dysfunction and deafness1 test
  • Ventricular fibrillation, paroxysmal familial, 21 test
  • Ventricular tachycardia1 test
  • Wolff-Parkinson-White pattern1 test
  • X-linked Emery-Dreifuss muscular dystrophy1 test

List of services

  • Custom Sequence Analysis
  • Insurance billing
  • Insurance preauthorization
  • Whole Exome Sequencing

List of certifications/licenses

Certifications

  • CLIAHelp, Number: 50D0631935, Expiration date: 2025-09-05
  • CAP, Number: 2463701, Expiration date: 2025-09-05

Participation in external programs

Standardization programs

  • Locus-specific Databases
  • Mutation-specific Databases
  • Other

Data exchange Programs

  • 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.