Genetic Testing List

Fairview Diagnostic Laboratories Genetics Test List May 2009 CPT codes are listed in the Lab Guide on each test

TestCode Name MD 11q23 Gene Rearrangement Molecular Detection Acute Myeloid Leukemia: Molecular Detection of the AML1/ETO Chimeric MD Transcript APOET ADmark ApoE Genotype Analysis & Interpretation (Symptomatic) Alpha-1-Antitrypsin and Alpha-1-Antitrypsin Genotype with Reflex to Alpha-1- LSMISC Antitrypsin Phenotype TTR Amyloidosis Evaluation Anaplastic Large Cell Lymphoma: Molecular Detection of the NPMA/ALK MD Chimeric Transcript APRTAT Aprataxin DNA Sequencing Test LSMISC Ashkenazi Jewish Carrier Testing AIRET Autoimmune Polyglandular Syndrome (AIRE) Evaluation ADATAT Autosomal Dominant Ataxia Evaluation MD bcl-1 Gene Rearrangement, Molecular Detection MD bcl-2 Gene Rearangement, Molecular Detection BCR-ABL: Molecular Detection of Major Breakpoint Region, CML Type, MD Quantitative BCR-ABL: Molecular Detection of Minor Breakpoint Region, ALL Type, MD Qualitative BRCA12 BRAC Analysis, BRCA1 and BRCA2 Gene

BRCAMM BRAC Analysis, Multiple Mutation BRCASM BRAC Analysis, Single Mutation MD BRAF V600E Mutation CAV3T Caveolin 3 DNA Sequencing Test CMT1A Charcot-Marie-Tooth 1A CMTX1 Charcot-Marie-Tooth X-Linked COMCMT Charcot-Marie-Tooth, Complete PCOL12 Collagen Genes 1 & 2 COMP Gene Analysis in Multiple Epiphyseal Dysplasia (MED) and LSMISC Pseudoachondroplasia (PSACH) CATAXT Complete Ataxia Evaluation CADAS Complete CADASIL Evaluation

COMSPG Complete Hereditary Spastic Paraplegia Evaluation MYOTON Complete Myotonia Evaluation CMDEI Complete Myotonic Dystrophy Evaluation CON26 Connexin 26 DNA Sequencing Test MD Cystathionine B-Synthase, Genotype (833 & 919) CFMA Cystic Fibrosis Mutation Analysis CFSCR Cystic Fibrosis Screening DRPLA Dentatorubrapallidotuysian Atrophy DNA Test DM2DNT DM2 DNA Test MD DNA Marker Engraftment, Graft vs Host MD DNA Marker, Post BMT Engraftment MD DNA Marker, Pre BMT Engraftment DOMCMT Dominant Charcot-Marie-Tooth Evaluation DYTI Dystonia (DYT1) DNA Emery-Dreifuss Muscular Dystrophy: emerin and/or lamin A/C Mutation MD Detection by Sequencing

MD Ewing's Sarcoma: Molecular Detection of the EWS/FLI-1 Chimeric Transcript

Please contact the Fairview Diagnostic Laboratories Genetics Counselor at 612-624-8948 with questions or concerns. Test pricing can be obtained at the Fairview Consumer Price Line 612-672-1048 Fairview Diagnostic Laboratories Genetics Test List May 2009 CPT codes are listed in the Lab Guide on each test

F2MA Factor 2 (Prothrombin) by PCR F5MA Factor 5 by PCR FALS Familial Amyotrophic Lateral Sclerosis (SOD1) DNA Test FHM1 Familial Hemiplegic Migraine Type 1 DNA Test CASRT Familial Hypocalciuric Hypercalcemia (CASR) Evaluation LSMISC Fibrillin-1 Gene FKRP FKRP DNA Sequencing Test MD FLT3 Mutation Assays for AML FRAGX Fragile X Molecular Analysis FDXT Friedreich's Ataxia DNA Test FSHD FSHD DNA Test MODY2 GCK (MODY2) DNA Sequencing Test GDAP1 GDAP1 DNA Sequencing Test MD Gene Rearrangement, B-Cell, Immunoglobulin Heavy Chain, PCR MD Gene Rearrangement, T-Cell Receptor, PCR GM1TAB GM1 Triad Autoantibody Test MD Hemochromatosis Mutation Analysis (S65C, C282Y and H63D) HNPP Hereditary Pressure Palsey Neuropathy IMM HLA-A, B and C Typing, HLA Class I (Allele Resolution) IMM HLA-A, B, and C Typing, HLA Class I (Low Resolution) IMM HLA-DR and DQ Typing, HLA Class II (Allele Resolution) IMM HLA-DR and DQ Typing, HLA Class II (Low Resolution) LSMISC HR2 Haplotype (Factor VHR2), A4070G Polymorphism Huntington Disease Molecular Analysis Contact Genetics MD Counselor at 612-624-8948 prior to collection. LSMISC Hurlers Mucolipidosis Type II Gene Sequencing MD JAK2 V617F Mutation KCNJ KCNJ11 (CH) DNA Sequencing Test KENDNA Kennedy's Disease DNA Test LHON Leber Optic LITAF LITAF/SIMPLE DNA Sequencing Test LRRK2 LRRK2 DNA Test MD Medium Chain Acyl-Co-A Dehydrogenase (Mutation Analysis) CMT2A MFN2 DNA Sequencing Test Microsatellite Instability Testing for Hereditary Nonpolyposis Colorectal Cancer MD Screen (HNPCC) MTDNA Mitochondrial DNA Disorder, Genetic Analysis LSMISC Mitochondrial Myopathy Screen, Muscle MD MTHFR Genotype MPZ Myelin Protein Zero (MPZ) DNA Sequencing MD Myotonic Dystrophy Molecular Analysis MD Myotonic Dystrophy Molecular Southern Analysis PANTP Neonatal Alloimmune Thrombocytopenia Investigation AVPR2 Nephrogenic Diabetes Insipidus Evaluation LSMISC Neurofibromatosis T1 NFT2 Neurofibromatosis Type 2 DNA Test NFL Neurofilament Light DNA Sequencing Test SPG6 NIPA (SPG6) DNA Sequencing Test NPH1 NPH1 (FJN) Molecular Analysis NPHS2 NPHS2 (Podocin) Sequencing Analysis MD Nucleophosmin (NPM1) Analysis OCA1, Oculocutaneous Albinism Type 1, Mutation Detection by DNA MD Sequencing

LSMISC Ornithine Transcarbamylase Mutation Carrier Analysis MD p53 Mutation Detection by DNA Sequencing PARKIN Parkin DNA Test CMTAXO Partial CMT - Axonal Only PCMTDM Partial CMT Evaluation - Demyelinating Only MD PAX2 Gene Mutation CMT4F Periaxin DNA Sequencing Test PINK1 PINK1 DNA Sequencing Test MD PKU Mutation Detection by DNA Sequencing LSMISC Platelet Antigen Genotyping, Level 1 MD PML/RAR: Molecular Detection of Acute Promyelocytic Leukemia PMPSEQ PMP22 DNA Sequencing Test LSMISC Prader Willi/Angelman Syndrome Analysis PWAS Prader-Willi/Angelman Syndrome Molecular Detection SCA1 SCA1 DNA Test SCA10 SCA10 DNA Test SCA14 SCA14 DNA Test SCA17 SCA17 DNA Test SCA2B SCA2B DNA Test SCA3 SCA3 DNA Test SCA5 SCA5 DNA Test SCA6 SCA6 DNA Test SCA7 SCA7 DNA Test SCA8 SCA8 DNA Test SETX SETX DNA Sequencing Test SMACT Spinal Atrophy LSMISC Spinal Muscular Atrophy DNA Test SMAD Spinal Muscular Atrophy Test TPMTGE TPMT Genetics (genotype) MD Warfarin Sensitivity by CYP2C9 and VKORC1 Genotyping

Please contact the Fairview Diagnostic Laboratories Genetics Counselor at 612-624-8948 with questions or concerns. Test pricing can be obtained at the Fairview Consumer Price Line 612-672-1048