What follows is from The ARUP Consult Test Fact Sheets.
Test Fact Sheets 1 A B C D E F G H I J K L M N O P R S T U V W X Y 1 1p/19q Deletion in Oligodendrogliomas A Acute Lymphoblastic Leukemia FISH Panels Acute Myeloid Leukemia Mutation Panel by Next Generation Sequencing Adalimumab and Antibodies to Adalimumab Quantitation Aldosterone-Renin Ratio Alloimmune Hemolytic Disease of the Fetus and Newborn (RhCc, RhEe, RhD, or Kell Antigen Genotyping) Alpha Thalassemia Alpha-1-Antitrypsin Deficiency Testing Alpha-Iduronidase Enzyme Activity in Leukocytes Alport Syndrome Panel, Sequencing and Deletion/Duplication Alzheimer’s Disease Markers, CSF Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA Ankylosing Spondylitis (HLA-B27) Genotyping Antinuclear Antibody (ANA) With HEp-2 Substrate Antiphospholipid Syndrome Reflex Panel Aortopathy Panel, Sequencing and Deletion/Duplication APC- and MUTYH-Associated Polyposis Panel, Sequencing and Deletion/Duplication Apolipoprotein E (APOE) Genotyping, Alzheimer Disease Risk Apolipoprotein E Genotyping, Cardiovascular Disease Risk Ashkenazi Jewish Genetic Diseases Panel Autism and Intellectual Disability Comprehensive Panel Autoimmune CNS Demyelinating Disease Reflexive Panel Autoimmune Dysautonomia Panel, Serum Autoimmune Encephalopathy and Dementia Panel, Serum and CSF Autoimmune Epilepsy Panel, Serum and CSF Autoimmune Movement Disorder Panel, Serum and CSF Autoimmune Myelopathy Panel, Serum and CSF Autoimmune Neurologic Disease Panel With Reflex, Serum and CSF Autoimmune Neuromuscular Junction Reflexive Panel Autoimmune Pediatric CNS Disorders Panel, Serum and CSF Autoimmune Stiff-Person Disorders Panel, Serum and CSF Autoimmune Vision Loss Panel, Serum B B-Cell Acute Lymphoblastic Leukemia Minimal Residual Disease Detection by Flow Cytometry BCR-ABL1 (BCR::ABL1) Qualitative and Quantitative Testing BCR-ABL1 Mutation Analysis for Tyrosine Kinase Inhibitor Resistance Beckwith-Wiedemann and Russell-Silver Syndromes Beta Globin (HBB) Sequencing Biotinidase Deficiency (BTD) Sequencing Birt-Hogg-Dubé Syndrome Borrelia burgdorferi Antibodies With Reflex to ELISA BRAF Mutation Detection C C1q Antibody, IgG Calprotectin, Fecal by Immunoassay Capillary Malformation-Arteriovenous Malformation Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication Celiac Disease HLA-DQ Genotyping Celiac Disease Reflexive Cascade, Serum Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, CADASIL (NOTCH3), Sequencing Cerebral Cavernous Malformation Panel, Sequencing and Deletion/Duplication Charcot-Marie-Tooth Disease and Related Hereditary Neuropathies Chimerism Testing by Short Tandem Repeat (STR) Genotyping Chromogenic Factor VIII, Activity Chronic Lymphocytic Leukemia Minimal Residual Disease Detection by Flow Cytometry Chronic Lymphocytic Leukemia Mutation Panel by Next Generation Sequencing Cobalamin/Propionate/Homocysteine Metabolism-Related Disorders Panel Colorectal Cancer Mutation Panel Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication Creatine Disorders Panel Testing CSF Bilirubin in Subarachnoid Hemorrhage CYFRA 21-1 (Cytokeratin 19 Fragment) in Lung Cancer CYP2D6 Cystic Fibrosis (CFTR) Expanded Variant Panel Cystic Fibrosis (CFTR) Sequencing and Deletion/Duplication Cytochrome P450 Genotyping Cytogenomic Microarray, Oncology Cytogenomic Microarray, Products of Conception Cytogenomic SNP Microarray Cytogenomic SNP Microarray, Fetal D Dermatomyositis and Polymyositis Panel Dermatomyositis Autoantibody Panel Diabetes-Associated Autoantibodies Dihydropyrimidine Dehydrogenase (DPYD) Dihydropyrimidine Dehydrogenase (DPYD) and UPD Glucuronosyltransferase 1A1 (UGT1A1) Genotyping Dilated Cardiomyopathy Panel, Sequencing Direct Xa Inhibitor Levels Distal Arthrogryposis Panel Drug Detection Panel Testing, Meconium and Umbilical Cord Tissue Drug Profile, Expanded Targeted Panels Drug Profiles, Targeted by Mass Spectrometry and Enzyme Immunoassay Duchenne/Becker Muscular Dystrophy E Early-Onset Alzheimer’s Panel, Sequencing Emery-Dreifuss Muscular Dystrophy Panel, Sequencing ERBB2 (HER2/neu) (HercepTest) Testing Ethyl Glucuronide, Umbilical Cord Tissue, Qualitative Exome Sequencing Extended Myositis Panel F Factor V Leiden (F5) R506Q Variant Factor XIII Deficiency Testing Familial Hypercholesterolemia Panel, Sequencing Familial Mediterranean Fever (MEFV) Sequencing Familial Transthyretin Amyloidosis (TTR) Sequencing Fatty Acid Oxidation Disorders Panel, Sequencing Fragile X (FMR1) With Reflex to Methylation Analysis G Galactosemia Genetic Testing Gamma Globin (HBG1 and HBG2) Sequencing Gaucher Disease Genetic Carrier Screen (CF, FXS, and SMA) With Reflex to Methylation Genital Ulcer Disease Panel Genome Sequencing Glucose-6-Phosphate Dehydrogenase Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency by DNA Glycogen Storage Disorders Panel, Sequencing H Hemochromatosis (HFE) 3 Variants Hemoglobin Evaluation Reflexive Cascade Hemophilia A (F8) Genetic Testing Hepatitis C Virus (HCV) NS5A Drug Resistance by Sequencing Hepatocellular Carcinoma Serum Markers Hereditary Bone Marrow Failure Panel, Sequencing and Deletion/Duplication Hereditary Breast and Gynecologic Cancers Panel Hereditary Breast Cancer Panels (Including BRCA1 and BRCA2) Hereditary Cancer Panel Hereditary Central Nervous System Cancer Panel, Sequencing and Deletion/Duplication Hereditary Erythrocytosis Panel, Sequencing Hereditary Gastric Cancer Panel, Sequencing and Deletion/Duplication Hereditary Gastrointestinal Cancer Panels Hereditary Hearing Loss – GJB2 and GJB6 Testing Hereditary Hemolytic Anemia Cascade Hereditary Hemolytic Anemia Panel, Sequencing Hereditary Hemorrhagic Telangiectasia Panel Hereditary Melanoma Panel, Sequencing and Deletion/Duplication Hereditary Myeloid Neoplasms Panel, Sequencing Hereditary Pancreatic Cancer Panel, Sequencing and Deletion/Duplication Hereditary Paraganglioma-Pheochromocytoma Panels Hereditary Prostate Cancer Panel, Sequencing and Deletion/Duplication Hereditary Renal Cancer Panel Hereditary Retinoblastoma (RB1) Sequencing and Deletion/Duplication Hereditary Thyroid Cancer Panel, Sequencing and Deletion/Duplication Heterotaxy and Situs Inversus Panel HLA-B*15:02 Genotyping, Carbamazepine Hypersensitivity HLA-B*57:01 for Abacavir Sensitivity HLA-B*58:01 Genotyping, Allopurinol Hypersensitivity Holoprosencephaly Panel, Sequencing and Deletion/Duplication Huntington Disease (HD) CAG Repeat Expansion Hypertrophic Cardiomyopathy Panel, Sequencing I IDH1-IDH2 Mutation Detection Infliximab and Antibodies to Infliximab Quantitation Interstitial Lung Disease Autoantibody Panel IRF4/DUSP22 Gene Rearrangement by FISH J JAK2 (V617F) Mutation by ddPCR K Kappa/Lambda Quantitative Free Light Chain With Ratio, Serum KIT Molecular Testing Kratom, Umbilical Cord Tissue, Qualitative L Leukemia/Lymphoma Phenotyping Evaluation by Flow Cytometry Loeys-Dietz Syndrome Core Panel, Sequencing Long QT Panel, Sequencing and Deletion/Duplication Lung Cancer Mutation Panel Lupus Anticoagulant Reflex Panel Lynch Syndrome Panel, Sequencing and Deletion/Duplication M Malignant Hyperthermia Panel, Sequencing Marfan Syndrome (FBN1) Sequencing and Deletion/Duplication Maternal Serum Screening Maturity-Onset Diabetes of the Young and Neonatal Diabetes Panel, Sequencing Measles Virus by Qualitative PCR Medium Chain Acyl-CoA Dehydrogenase (ACADM) 2 Variants Melanoma Mutation Panel Methylenetetrahydrofolate Reductase (MTHFR) Testing Multiple Endocrine Neoplasia Type 1 (MEN1) Sequencing and Deletion/Duplication Multiple Endocrine Neoplasia Type 2, RET Sequencing Multiple Myeloma Minimal Residual Disease Detection by Flow Cytometry Multiple Myeloma Panel by FISH Myasthenia Gravis Testing MYD88 L265P Mutation Detection by PCR, Quantitative Myeloid Malignancies Mutation and Copy Number Variation Panel by Next Generation Sequencing Myotonic Dystrophy Type 1 (DMPK) N Neurofibromatosis Type 1 and Legius Syndrome Panel, Sequencing and Deletion/Duplication Noninvasive Prenatal Aneuploidy Screen by Cell-Free DNA Sequencing Noonan Spectrum Disorders Panel O Opioid Receptor, mu OPRM1 Genotype, 1 Variant Osteogenesis Imperfecta and Low Bone Density Panel, Sequencing P Pancreatitis Panel Paraneoplastic Reflexive Panel, Serum and CSF Paroxysmal Nocturnal Hemoglobinuria Testing PD-L1 by Immunohistochemistry Periodic Fever Syndromes Panel, Sequencing and Deletion/Duplication Peroxisomal Disorders Panel, Sequencing Pharmacogenetics Panel for Psychotropics Phospho-Tau 217, Plasma Plasminogen Activator Inhibitor-1 (SERPINE1) Genotyping Platelet Antigen Genotyping Panel Pneumonia Panel by PCR Polymyositis Panel Primary Antibody Deficiency Panel, Sequencing and Deletion/Duplication Primary Ciliary Dyskinesia Panel Primary Membranous Nephropathy Comprehensive Autoantibody Panel Procalcitonin Prolonged Clot Time Reflexive Profile Prothrombin (F2) c.*97G>A (G20210A) Pathogenic Variant Pulmonary Arterial Hypertension Panel, Sequencing and Deletion/Duplication R Rapid Acute Myeloid Leukemia Targeted Therapy Mutation Panel RBC Band 3 Protein Reduction in Hereditary Spherocytosis Red Blood Cell Antigen Genotyping Respiratory Pathogen Molecular Panel Testing S SHOX Deficiency Disorders, Sequencing and Deletion/Duplication Shwachman-Diamond Syndrome Skeletal Dysplasia Panel, Sequencing and Deletion/Duplication Solid Tumor Mutation Panel, Sequencing Soluble Mesothelin-Related Peptides (MESOMARK) Spinal Muscular Atrophy Copy Number Analysis Stickler Syndrome Panel, Sequencing Succinylacetone, Quantitative, Urine – Tyrosinemia Type 1 T Tay-Sachs Disease (HEXA) Sequencing and Deletion/Duplication TFE3 (Xp11.2) Gene Rearrangement by FISH Thiopurine Metabolites in Red Blood Cells Thiopurine Methyltransferase, RBC Thrombotic Risk Reflex Panel Toll-Like Receptor Function Testing TPMT and NUDT15 TPSAB1 Copy Number Analysis by ddPCR Tuberous Sclerosis Complex Panel, Sequencing and Deletion/Duplication U UGT1A1 Gene Analysis Urticaria-Inducing Activity and Urticaria-Induced Basophil Activation V Vaginitis Panel by TMA Vascular Malformations Panel, Sequencing and Deletion/Duplication Very Long-Chain Acyl-CoA Dehydrogenase (ACADVL) Deficiency Very Long-Chain and Branched-Chain Fatty Acids Profile Von Willebrand Disease (VWF) Sequencing W Warfarin Sensitivity (CYP2C9, CYP2C cluster, CYP4F2, VKORC1) Genotyping Wilson Disease (ATP7B) Sequencing X X-Chromosome Inactivation Analysis Y Y Chromosome Microdeletions
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