NY State Informed Consent Tests
New York State clients are required by New York State regulations to have completed informed-consent forms on file. When ordering the following tests, all NYS clients are required to indicate to Mayo Clinic Laboratories that informed consent has been obtained.
- GAAWR | Acid Alpha-Glucosidase Reflex, Leukocytes
- GAAW | Acid Alpha-Glucosidase, Leukocytes
- ASMW | Acid Sphingomyelinase, Leukocytes
- APGP | Acute Porphyria Gene Panel, Varies
- ALAGP | Alagille Syndrome Gene Panel, Varies
- WAGDR | Alpha Globin Cluster Locus Deletion/Duplication, Blood
- AGDD | Alpha Globin Cluster Locus Deletion/Duplication, Varies
- WASEQ | Alpha Globin Gene Sequencing, Varies
- FUCW | Alpha-Fucosidase, Leukocytes
- AGABS | Alpha-Galactosidase, Blood Spot
- AGAW | Alpha-Galactosidase, Leukocytes
- AGAS | Alpha-Galactosidase, Serum
- WASQR | Alpha-Globin Gene Sequencing, Blood
- IDUAW | Alpha-L-Iduronidase, Leukocytes
- MANN | Alpha-Mannosidase, Leukocytes
- ALPGP | Alport Syndrome Gene Panel, Varies
- AIHL | Aminoglycoside-Induced Hearing Loss, Targeted Variant Testing, Droplet Digital PCR, Varies
- ALADW | Aminolevulinic Acid Dehydratase, Washed Erythrocytes
- ALAD | Aminolevulinic Acid Dehydratase, Whole Blood
- AECDP | Angioedema and Complement Disorders Gene Panel, Varies
- GNANT | Antithrombin Deficiency, SERPINC1 Gene, Next-Generation Sequencing, Varies
- APOL1 | APOL1 Genotype, Varies
- APOEG | Apolipoprotein E Genotyping, Blood
- ARVGG | Arrhythmogenic Cardiomyopathy Gene Panel, Varies
- ARSU | Arylsulfatase A, 24 Hour, Urine
- ARSAW | Arylsulfatase A, Leukocytes
- ARSBB | Arylsulfatase B, Blood Spot
- ARSBW | Arylsulfatase B, Leukocytes
- AHUGP | Atypical Hemolytic Uremic Syndrome (aHUS)/Thrombotic Microangiopathy (TMA) /Complement 3 Glomerulopathy (C3G) Gene Panel, Varies
- AHLP | AudioloGene Hearing Loss Panel, Varies
- ALPSG | Autoimmune Lymphoproliferative Syndrome (ALPS) Gene Panel, Varies
- AUTOG | Autoinflammatory Disorders Gene Panel, Varies
- BAP1Z | BAP1-Tumor Predisposition Syndrome, BAP1 Full Gene Analysis, Varies
- RBART | Bartter Syndrome Gene Panel, Varies
- BCELL | B-Cell and Antibody Deficiency Gene Panel, Varies
- BWRS | Beckwith-Wiedemann Syndrome/Russell-Silver Syndrome, Molecular Analysis, Varies
- WBSEQ | Beta Globin Gene Sequencing, Varies
- BGA | Beta-Galactosidase, Leukocytes
- WBGDR | Beta-Globin Gene Cluster Deletion/Duplication, Blood
- WBGDD | Beta-Globin Gene Cluster, Deletion/Duplication, Varies
- WBSQR | Beta-Globin Gene Sequencing, Blood
- GBAW | Beta-Glucosidase, Leukocytes
- GUSBB | Beta-Glucuronidase, Blood Spot
- GUSBW | Beta-Glucuronidase, Leukocytes
- BTDZ | Biotinidase Deficiency, BTD Full Gene Analysis, Varies
- BIOTS | Biotinidase, Serum
- BHDZ | Birt-Hogg-Dube Syndrome, FLCN, Full Gene Analysis, Varies
- GNBLC | Bleeding Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies
- GNBLF | Bleeding Disorders, Focused Gene Panel, Next-Generation Sequencing, Varies
- HBOCZ | BRCA1/BRCA2 Genes, Full Gene Analysis, Varies
- SCN5A | Brugada Syndrome, SCN5A Full Gene Analysis, Varies
- BTKSG | Bruton Tyrosine Kinase, BTK Full Gene Analysis, Varies
- C9ORF | C9orf72 Hexanucleotide Repeat, Molecular Analysis, Varies
- CARBR | Carbamazepine Hypersensitivity Pharmacogenomics, Varies
- CSFP | Carrier Screen, Focused Panel, Varies
- CASRG | CASR Full Gene Sequencing with Deletion/Duplication, Varies
- CPVTG | Catecholaminergic Polymorphic Ventricular Tachycardia Gene Panel, Varies
- COMTQ | Catechol-O-Methyltransferase (COMT) Genotype, Varies
- CDKZ | CDKN1C Gene, Full Gene Analysis, Varies
- CHLGP | Cholestasis Gene Panel, Varies
- CMAPC | Chromosomal Microarray, Autopsy, Products of Conception, or Stillbirth
- CMAMT | Chromosomal Microarray, Autopsy/Products of Conception/Stillbirth, Tissue
- CMACB | Chromosomal Microarray, Congenital, Blood
- CMAP | Chromosomal Microarray, Prenatal, Amniotic Fluid/Chorionic Villus Sampling
- CHRAF | Chromosome Analysis, Amniotic Fluid
- CHRCV | Chromosome Analysis, Chorionic Villus Sampling
- CHRCB | Chromosome Analysis, Congenital Disorders, Blood
- CHRTI | Chromosome Analysis, Skin Biopsy
- COMID | Combined Humoral and Cell-Mediated Immunodeficiency Gene Panel, Varies
- CMITO | Combined Mitochondrial Full Genome and Nuclear Gene Panel, Varies
- CACMG | Comprehensive Arrhythmia and Cardiomyopathy Gene Panel, Varies
- CARGG | Comprehensive Arrhythmia Gene Panel, Varies
- CCMGG | Comprehensive Cardiomyopathy Gene Panel, Varies
- CVHBG | Comprehensive Cerebrovascular Gene Panel, Varies
- DWPAN | Comprehensive Distal Weakness Gene Panel, Varies
- EPPAN | Comprehensive Epilepsy With or Without Encephalopathy Gene Panel, Varies
- CAORG | Comprehensive Marfan, Loeys-Dietz, Ehlers-Danlos, and Aortopathy Gene Panel, Varies
- NEPHP | Comprehensive Nephrology Gene Panel, Varies
- MUPAN | Comprehensive Neuromuscular Gene Panel, Varies
- PEPAN | Comprehensive Peripheral Neuropathy Gene Panel, Varies
- CDGGP | Congenital Disorders of Glycosylation Gene Panel, Varies
- NCDA | Congenital Dyserythropoietic Anemia Gene Panel, Next-Generation Sequencing, Varies
- GNFIB | Congenital Fibrinogen Disorders, FGA, FGB, and FGG Genes, Next-Generation Sequencing, Varies
- CHDGG | Congenital Heart Disease Gene Panel, Varies
- CLADP | Congenital Lactic Acidosis Panel, Varies
- CSTB | CSTB Gene, Repeat Expansion Analysis, Varies
- CGPH | Custom Gene Panel, Hereditary, Next-Generation Sequencing, Varies
- CFSMN | Cystic Fibrosis and Spinal Muscular Atrophy Carrier Screen Panel, Varies
- CFTRN | Cystic Fibrosis Transmembrane Conductance Regulator, CFTR, Full Gene Analysis, Varies
- CFMP | Cystic Fibrosis, CFTR Gene, Variant Panel, Varies
- CKDGP | Cystic Kidney Disease Gene Panel, Varies
- CYSGP | Cystinuria Gene Panel, Varies
- 1A2Q | Cytochrome P450 1A2 Genotype, Varies
- 2B6Q | Cytochrome P450 2B6 Genotype, Varies
- 2C19R | Cytochrome P450 2C19 Genotype, Varies
- 2C9QT | Cytochrome P450 2C9 Genotype, Varies
- 2D6Q | Cytochrome P450 2D6 Comprehensive Cascade, Varies
- 3A4Q | Cytochrome P450 3A4 Genotype, Varies
- 3A5Q | Cytochrome P450 3A5 Genotype, Varies
- DRPL | Dentatorubral-Pallidoluysian Atrophy (DRPLA) Gene Analysis, Varies
- DPYDQ | Dihydropyrimidine Dehydrogenase Genotype, Varies
- DPYDZ | Dihydropyrimidine Dehydrogenase, DPYD Full Gene Sequencing, Varies
- DCLNG | Dilated Cardiomyopathy and Left Ventricular Noncompaction Cardiomyopathy Gene Panel, Varies
- DMDZ | DMD Gene, Full Gene Analysis, Varies
- DBMD | Duchenne/Becker Muscular Dystrophy, DMD Gene, Large Deletion/Duplication Analysis, Varies
- EOIBD | Early Onset Monogenic Inflammatory Bowel Disease (IBD) Gene Panel, Varies
- EDSGG | Ehlers-Danlos Syndrome Gene Panel, Varies
- EBLPD | Epstein Barr Virus (EBV) Susceptibility and Lymphoproliferative Disorders Gene Panel, Varies
- REVE2 | Erythrocytosis Evaluation, Blood
- EPOR | Erythropoietin Receptor (EPOR) Gene, Exon 8 Sequencing, Whole Blood
- PANGP | Expanded Pancreatitis Gene Panel, Varies
- FABRZ | Fabry Disease, Full Gene Analysis, Varies
- F5DNA | Factor V Leiden (R506Q) Mutation, Blood
- GNF7 | Factor VII Deficiency, F7 Gene, Next-Generation Sequencing, Varies
- GNF13 | Factor XIII Deficiency, F13A1 and F13B Genes, Next-Generation Sequencing, Varies
- FMTT | Familial Variant, Targeted Testing, Varies
- CMPRE | Family Member Comparator Specimen for Exome Sequencing, Varies
- CMPRG | Family Member Comparator Specimen for Genome Sequencing, Varies
- HFAOP | Fatty Acid Oxidation Gene Panel, Varies
- FAO | Fatty Acid Oxidation Probe Assay, Fibroblast Culture
- MFBNG | FBN1 Full Gene Sequencing with Deletion/Duplication, Varies
- RFSGS | Focal Segmental Glomerulosclerosis (FSGS) and Nephrotic Syndrome Gene Panel, Varies
- ADPKP | Focused Autosomal Dominant Polycystic Kidney Disease Gene Panel, Varies
- PGXQP | Focused Pharmacogenomics Panel, Varies
- FXS | Fragile X Syndrome, Molecular Analysis, Varies
- FFRWB | Friedreich Ataxia, Frataxin, Quantitative, Blood
- FFRBS | Friedreich Ataxia, Frataxin, Quantitative, Blood Spot
- AFXN | Friedreich Ataxia, Repeat Expansion Analysis, Varies
- GALCR | Galactocerebrosidase Reflex, Leukocytes
- GALCW | Galactocerebrosidase, Leukocytes
- GALK | Galactokinase, Blood
- GALTP | Galactose-1-Phosphate Uridyltransferase Biochemical Phenotyping, Erythrocytes
- GALT | Galactose-1-Phosphate Uridyltransferase, Blood
- GCT | Galactosemia Reflex, Blood
- GALZ | Galactosemia, GALT Gene, Full Gene Analysis, Varies
- GALMP | Galactosemia, GALT Gene, Variant Panel, Varies
- WGSEQ | Gamma-Globin Full Gene Sequencing, Varies
- GATAS | GATA-Binding Protein 2, GATA2, Full Gene Analysis, Next-Generation Sequencing, Varies
- GBAZ | Gaucher Disease, Full Gene Analysis, Varies
- G6PDZ | Glucose-6-Phosphate Dehydrogenase (G6PD) Full Gene Sequencing, Varies
- GA2P | Glutaric Aciduria Type II Gene Panel, Varies
- GSDGP | Glycogen Storage Disease Gene Panel, Varies
- HMEP | Hemiplegic Migraine With or Without Epilepsy Gene Panel, Varies
- HBEL1 | Hemoglobin Electrophoresis Evaluation, Blood
- HAEV1 | Hemolytic Anemia Evaluation, Blood
- F8INP | Hemophilia A F8 Gene, Intron 1 and 22 Inversion Mutation Analysis, Prenatal
- F8INV | Hemophilia A F8 Gene, Intron 1 and 22 Inversion Mutation Analysis, Whole Blood
- F81P | Hemophilia A F8 Gene, Intron 1 Inversion Known Mutation Analysis, Prenatal
- F81B | Hemophilia A F8 Gene, Intron 1 Inversion Known Mutation, Whole Blood
- F822B | Hemophilia A F8 Gene, Intron 22 Inversion Known Mutation, Whole Blood
- F822P | Hemophilia A F8 Gene, Intron 22 Inversion Mutation Analysis, Prenatal
- GNHMA | Hemophilia A, F8 Gene, Next-Generation Sequencing, Varies
- GNHMB | Hemophilia B, F9 Gene, Next-Generation Sequencing, Varies
- GNF11 | Hemophilia C (Factor XI Deficiency), F11 Gene, Next-Generation Sequencing, Varies
- GNANG | Hereditary Angioedema Focused Gene Panel, Next-Generation Sequencing, Varies
- BRGYP | Hereditary Breast/Gynecologic Cancer Panel, Varies
- COMCP | Hereditary Common Cancer Panel, Varies
- CDHZ | Hereditary Diffuse Gastric Cancer Syndrome, CDH1, Full Gene Analysis, Varies
- ENDCP | Hereditary Endocrine Cancer Panel, Varies
- NHEM | Hereditary Erythrocytosis Focused Gene Panel, Next-Generation Sequencing, Varies
- NHEP | Hereditary Erythrocytosis Gene Panel, Next-Generation Sequencing, Varies
- HEMP | Hereditary Erythrocytosis Mutations, Whole Blood
- XCP | Hereditary Expanded Cancer Panel, Varies
- CRCGP | Hereditary Gastrointestinal Cancer Panel, Varies
- HFET | Hereditary Hemochromatosis, HFE Variant Analysis, Varies
- NHHA | Hereditary Hemolytic Anemia Gene Panel, Next-Generation Sequencing, Varies
- HHTGG | Hereditary Hemorrhagic Telangiectasia and Vascular Malformations Gene Panel, Varies
- LRCCZ | Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome, FH, Full Gene Analysis, Varies
- PANCP | Hereditary Pancreatic Cancer Panel, Varies
- HPANP | Hereditary Pancreatitis Gene Panel, Varies
- HPGLP | Hereditary Paraganglioma/Pheochromocytoma Panel, Varies
- PRS8P | Hereditary Prostate Cancer Panel, Varies
- RENCP | Hereditary Renal Cancer Panel, Varies
- GNHTC | Hereditary Thrombocytopenia Gene Panel, Next-Generation Sequencing, Varies
- GNADM | Hereditary Thrombotic Thrombocytopenic Purpura, ADAMTS13 Gene, Next-Generation Sequencing, Varies
- THYRP | Hereditary Thyroid Cancer Panel, Varies
- WILMP | Hereditary Wilms Tumor Panel, Varies
- NAGW | Hexosaminidase A and Total Hexosaminidase, Leukocytes
- NAGS | Hexosaminidase A and Total Hexosaminidase, Serum
- NAGR | Hexosaminidase A and Total, Leukocytes/Molecular Reflex, Whole Blood
- MUGS | Hexosaminidase A, Serum
- HL57R | HLA-B*57:01 Genotype, Pharmacogenomics, Varies
- HL58R | HLA-B*5801 Genotype, Allopurinol Hypersensitivity, Varies
- MPS2Z | Hunter Syndrome, Full Gene Analysis, Varies
- HAD | Huntington Disease, Molecular Analysis, Varies
- MPS1Z | Hurler Syndrome, Full Gene Analysis, Varies
- HCHLG | Hypercholesterolemia Gene Panel, Varies
- HIESG | Hyper-IgE Syndrome Gene Panel, Varies
- HYPTG | Hypertriglyceridemia Gene Panel, Varies
- HCMGG | Hypertrophic Cardiomyopathy Gene Panel, Varies
- HYPBG | Hypobetalipoproteinemia Gene Panel, Varies
- HIF2A | Hypoxia-Inducible Factor Alpha (EPAS1/HIF2A) Gene, Exons 9 and 12 Sequencing, Whole Blood
- IPFGP | Idiopathic Pulmonary Fibrosis Gene Panel, Varies
- I2SB | Iduronate-2-Sulfatase, Blood Spot
- I2SWB | Iduronate-2-Sulfatase, Leukocytes
- IMMAU | Inborn Errors of Immunity with Immune Dysregulation and Autoimmunity Gene Panel, Varies
- INFXP | Infliximab Quantitation with Antibodies to Infliximab, Serum
- ATAXP | Inherited Ataxia Gene Panel, Varies
- BMFGP | Inherited Bone Marrow Failure Gene Panel, Varies
- CMSP | Inherited Congenital Myasthenic Syndrome Gene Panel, Varies
- EDMDP | Inherited Emery-Dreifuss Gene Panel, Varies
- AFTDP | Inherited Frontotemporal Dementia and Amyotrophic Lateral Sclerosis Gene Panel, Varies
- LGCMP | Inherited Limb-Girdle Muscular Dystrophy and Congenital Myasthenic Syndrome Gene Panel, Varies
- IMSNP | Inherited Motor and Sensory Neuropathy Gene Panel, Varies
- MNDP | Inherited Motor Neuron Disease Gene Panel, Varies
- IMNP | Inherited Motor Neuropathy Gene Panel, Varies
- MDYSP | Inherited Muscular Dystrophy Gene Panel, Varies
- PARDP | Inherited Parkinson Disease Gene Panel, Varies
- RABMP | Inherited Rhabdomyolysis and Metabolic Myopathy Panel, Varies
- ISNP | Inherited Sensory Neuropathy Gene Panel, Varies
- SMCP | Inherited Skeletal Muscle Channelopathy Gene Panel, Varies
- ISPP | Inherited Spastic Paraplegia Gene Panel, Varies
- IL28Q | Interleukin 28B (IL28B) Variant (rs12979860), Varies
- LIPOG | Lipodystrophy Gene Panel, Varies
- LQTSG | Long QT Syndrome Gene Panel, Varies
- LYNCP | Lynch Syndrome Panel, Varies
- LALB | Lysosomal Acid Lipase, Blood
- LALBS | Lysosomal Acid Lipase, Blood Spot
- PLSD | Lysosomal and Peroxisomal Disorders Screen, Blood Spot
- LSDGP | Lysosomal Storage Disease Gene Panel, Varies
- LSD6W | Lysosomal Storage Disorders, Six-Enzyme Panel, Leukocytes
- GNMTC | Macro/Microthrombocytopenia Gene Panel, Next-Generation Sequencing, Varies
- MSUDP | Maple Syrup Urine Disease Gene Panel, Varies
- MFRGG | Marfan, Loeys-Dietz, and Aortopathy Gene Panel, Varies
- MATCC | Maternal Cell Contamination, Molecular Analysis, Varies
- MCP2Z | MECP2 Gene, Full Gene Analysis, Varies
- MCADZ | Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Full Gene Analysis, Varies
- MEV1 | Methemoglobinemia Evaluation, Blood
- MMAGP | Methylmalonic Aciduria Gene Panel, Varies
- MPAGP | Methylmalonic Aciduria-Propionic Aciduria Combined Gene Panel, Varies
- DMITO | Mitochondrial DNA Deletion Heteroplasmy, ddPCR, Varies
- MITOP | Mitochondrial Full Genome Analysis, Next-Generation Sequencing (NGS), Varies
- MLHPB | MLH1 Hypermethylation Analysis, Blood
- MP8BS | Mucopolysaccharidoses, Eight-Enzyme Panel, Blood Spot
- MP9W | Mucopolysaccharidoses, Nine-Enzyme Panel, Leukocytes
- MPS3W | Mucopolysaccharidosis III, Four-Enzyme Panel, Leukocytes
- MPS3B | Mucopolysaccharidosis III, Three-Enzyme Panel, Blood Spot
- MPS4B | Mucopolysaccharidosis IV Enzyme Panel, Blood Spot
- MPS4W | Mucopolysaccharidosis IV Enzyme Panel, Leukocytes
- RETZZ | Multiple Endocrine Neoplasia Type 2 Syndrome, RET, Full Gene Analysis, Varies
- MSDBS | Multiple Sulfatase Deficiency, Blood Spot
- MSDW | Multiple Sulfatase Deficiency, Leukocytes
- GNMY9 | MYH9-Related Disorders, MYH9 Gene, Next-Generation Sequencing, Varies
- NAT2Q | N-Acetyltransferase 2 (NAT2) Genotype, Varies
- RSCGP | Nephrocalcinosis, Nephrolithiasis, and Renal Electrolyte Imbalance Gene Panel, Varies
- NF1Z | Neurofibromatosis Type 1, NF1, Full Gene Analysis, Varies
- NCLGP | Neuronal Ceroid Lipofuscinosis (Batten Disease) Gene Panel, Varies
- NCLBS | Neuronal Ceroid Lipofuscinosis, Two-Enzyme Panel, Blood Spot
- NCLW | Neuronal Ceroid Lipofuscinosis, Two-Enzyme Panel, Leukocytes
- NADF | Newborn Aneuploidy Detection, FISH, Blood
- NSRGG | Noonan Syndrome and Related Conditions Gene Panel, Varies
- NTC3Z | NOTCH3 Gene, Full Gene Analysis, Varies
- NMITO | Nuclear Mitochondrial Gene Panel, Next-Generation Sequencing, Varies
- WESPR | Panel to Whole Exome Sequencing Reflex Test, Varies
- PDGP | Peroxisomal Disorder Gene Panel, Varies
- STK1Z | Peutz-Jeghers Syndrome, STK11, Full Gene Analysis, Varies
- PHCGD | Phagocytic Disorders and Chronic Granulomatous Disease Gene Panel, Varies
- PHEGP | Phenylalanine Disorders Gene Panel, Varies
- PMMIL | Phosphomannomutase and Phosphomannose Isomerase, Leukocytes
- PKLRZ | PKLR Full Gene Analysis, Varies
- GNPLT | Platelet Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies
- GNPFD | Platelet Function Defect Gene Panel, Next-Generation Sequencing, Varies
- GNSPD | Platelet Storage Pool Deficiency Gene Panel, Next-Generation Sequencing, Varies
- PMPDD | PMP22 Gene, Large Deletion/Duplication Analysis, Varies
- PD2T | Pompe Disease Second-Tier Newborn Screening, Blood Spot
- PDBS | Pompe Disease, Blood Spot
- GAAZ | Pompe Disease, Full Gene Analysis, Varies
- PBGDW | Porphobilinogen Deaminase, Washed Erythrocytes
- PBGD_ | Porphobilinogen Deaminase, Whole Blood
- PCGP | Porphyria Comprehensive Gene Panel, Varies
- PMAOG | Postmortem Aortopathy Gene Panel, Tissue
- PMARG | Postmortem Arrhythmia Gene Panel, Tissue
- PMCAG | Postmortem Cardiomyopathy and Arrhythmia Gene Panel, Tissue
- PMCMG | Postmortem Cardiomyopathy Gene Panel, Tissue
- PCMSP | Postmortem Inherited Congenital Myasthenia Syndrome Gene Panel, Tissue
- PMHLH | Postmortem Primary Hemophagocytic Lymphohistiocytosis (HLH) Gene Panel, Tissue
- PWAS | Prader-Willi/Angelman Syndrome, Molecular Analysis, Varies
- PADF | Prenatal Aneuploidy Detection, FISH
- PCDGG | Primary Ciliary Dyskinesia Gene Panel, Varies
- HLHGP | Primary Hemophagocytic Lymphohistiocytosis Gene Panel, Varies
- PRKSG | PRKAR1A Full Gene Sequencing with Deletion/Duplication, Varies
- PHD2 | Prolyl Hydroxylase Domain-2 (PHD2/EGLN1) Gene Sequencing, Whole Blood
- FIBDD | PROMETHEUS IBD sgi Diagnostic
- GNPRC | Protein C Deficiency, PROC Gene, Next-Generation Sequencing, Varies
- GNPRS | Protein S Deficiency, PROS1 Gene, Next-Generation Sequencing, Varies
- PTNT | Prothrombin G20210A Mutation, Blood
- PRSSZ | PRSS1 Gene, Full Gene Analysis, Varies
- PSYQP | Psychotropic Pharmacogenomics Gene Panel, Varies
- PTNZ | PTEN Hamartoma Tumor Syndrome, PTEN Full Gene Analysis, Varies
- BRTP | Rapid Hereditary Breast Cancer Treatment Decision Panel, Varies
- NCYB | Recessive Congenital Methemoglobinemia, CYB5 and CYB5 Reductase Genetic Analysis, Next-Generation Sequencing, Varies
- NENZ | Red Blood Cell Enzyme Disorders Gene Panel, Next-Generation Sequencing, Varies
- NMEM | Red Blood Cell Membrane Disorders Gene Panel, Next-Generation Sequencing, Varies
- HEXBZ | Sandhoff Disease, HEXB Gene, Full Gene Analysis, Varies
- SEP9Z | SEPTIN9 Gene, Full Gene Analysis, Varies
- SERPZ | SERPINA1 Gene, Full Gene Analysis, Varies
- SCIDP | Severe Combined Immunodeficiency (SCID) Gene Panel, Varies
- SCCNP | Severe Congenital and Cyclic Neutropenia Gene Panel, Varies
- SCTF | Sex Chromosome Determination, FISH, Tissue
- SRYF | Sex-Determining Region Y, Yp11.3 Deletion, FISH
- SQTSG | Short QT Syndrome Gene Panel, Varies
- DHCRZ | Smith Lemli Opitz Syndrome, DHCR7 Gene, Full Gene Analysis, Varies
- SMN1Z | SMN1 Gene, Full Gene Analysis, Varies
- SOD1Z | SOD1 Gene, Full Gene Analysis, Varies
- SLC1Q | Solute Carrier Organic Anion Transporter Family Member 1B1 (SLCO1B1) Genotype, Statin, Varies
- SMNCS | Spinal Muscular Atrophy Carrier Screening, Deletion/Duplication Analysis, Varies
- SMNDX | Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies
- SBULB | Spinobulbar Muscular Atrophy (Kennedy Disease), Molecular Analysis, Varies
- SCAP | Spinocerebellar Ataxia Repeat Expansion Panel, Varies
- SCARA | Spinocerebellar Ataxia Type 1, 2, 3, 6, or 7, Repeat Expansion Analysis, Varies
- HEXAZ | Tay-Sachs Disease, HEXA Gene, Full Gene Analysis, Varies
- TELDP | Telomere Biology Disorders Gene Panel, Varies
- THEV1 | Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
- TPNUQ | Thiopurine Methyltransferase (TPMT) and Nudix Hydrolase (NUDT15) Genotyping, Varies
- TPMT3 | Thiopurine Methyltransferase Activity Profile, Erythrocytes
- AATHR | Thrombophilia Profile, Plasma and Whole Blood
- GNTHR | Thrombosis Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies
- TTRZ | TTR Gene, Full Gene Analysis, Varies
- TSCP | Tuberous Sclerosis Gene Panel, Varies
- TYRGP | Tyrosine Disorders Gene Panel, Varies
- UGTFZ | UDP-Glucuronosyltransferase 1A1 (UGT1A1), Full Gene Sequencing, Varies
- UNIPD | Uniparental Disomy, Varies
- UCDP | Urea Cycle Disorders Gene Panel, Varies
- U1A1Q | Uridine Diphosphate (UDP) Glucuronosyltransferase 1A1 TA Repeat Genotype, UGT1A1, Varies
- GALE | Uridine Diphosphate-Galactose 4' Epimerase, Blood
- UPGDW | Uroporphyrinogen Decarboxylase, Washed Erythrocytes
- UPGD | Uroporphyrinogen Decarboxylase, Whole Blood
- UPGC | Uroporphyrinogen III Synthase (Co-Synthase), Erythrocytes
- VLCZ | Very Long Chain Acyl-CoA Dehydrogenase Deficiency, Full Gene Analysis, Varies
- VHLE | VHL Gene, Erythrocytosis, Mutation Analysis, Varies
- VIRID | Viral Susceptibility, Defects in Intrinsic and Innate Immunity, Gene Panel, Varies
- VHLZZ | Von Hippel Lindau Syndrome, VHL, Full Gene Analysis, Varies
- GNVWD | von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies
- WARSQ | Warfarin Response Genotype, Varies
- WESMT | Whole Exome and Mitochondrial Genome Sequencing, Varies
- WESDX | Whole Exome Sequencing for Hereditary Disorders, Varies
- WGSDX | Whole Genome Sequencing for Hereditary Disorders, Varies
- WNDZ | Wilson Disease, ATP7B Full Gene Sequencing with Deletion/Duplication, Varies