ClinVar Miner

Variants in gene SCN5A

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Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
425 350 2419 1595 264 601 4553

Condition and significance breakdown #

Total conditions: 107
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
not provided 323 181 1651 1198 168 54 3275
Cardiac arrhythmia 40 40 1090 711 46 0 1907
Cardiovascular phenotype 84 74 572 531 29 0 1267
Brugada syndrome 1 56 65 224 66 34 267 605
not specified 1 2 173 240 139 0 476
Brugada syndrome 39 65 81 21 5 209 391
Long QT syndrome 3 27 20 135 33 27 0 236
Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1; Progressive familial heart block, type 1A; Ventricular fibrillation, paroxysmal familial, type 1; Dilated cardiomyopathy 1E; SUDDEN INFANT DEATH SYNDROME; Atrial fibrillation, familial, 10 14 18 168 9 4 0 211
Dilated cardiomyopathy 1E 7 4 140 29 15 0 192
Sick sinus syndrome 1 9 3 113 14 40 0 179
Congenital long QT syndrome 4 4 5 0 1 160 171
Progressive familial heart block, type 1A 5 0 128 27 11 0 170
Ventricular fibrillation, paroxysmal familial, type 1 1 0 123 28 13 0 165
SCN5A-related disorder 8 15 33 43 3 5 105
Cardiomyopathy 0 1 23 12 25 0 58
Long QT syndrome 7 4 22 4 3 0 38
Primary dilated cardiomyopathy 1 3 18 2 8 6 35
Brugada syndrome 1; Long QT syndrome 3 3 10 9 2 1 1 25
Brugada syndrome (shorter-than-normal QT interval) 8 6 0 0 0 0 14
Atrial fibrillation 0 2 3 1 0 10 13
Atrial fibrillation, familial, 10 8 0 3 0 0 0 11
Primary familial hypertrophic cardiomyopathy 0 0 11 0 0 0 11
SUDDEN INFANT DEATH SYNDROME 1 1 4 0 0 3 9
Arrhythmogenic right ventricular cardiomyopathy 1 0 6 1 0 0 8
Brugada syndrome 1; Long QT syndrome 3; Dilated cardiomyopathy 1E 2 5 1 0 0 0 8
Conduction system disorder 1 0 1 0 0 5 7
See cases 0 0 1 3 3 0 7
Familial isolated arrhythmogenic right ventricular dysplasia 6 0 0 0 0 0 6
Long QT syndrome 3; Brugada syndrome 0 0 4 0 2 0 6
Primary familial dilated cardiomyopathy 3 0 2 0 0 0 5
Hypertrophic cardiomyopathy 0 0 4 0 0 0 4
Ventricular tachycardia 0 1 1 1 0 1 4
Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1; Dilated cardiomyopathy 1E; SUDDEN INFANT DEATH SYNDROME 0 0 0 0 0 3 3
Brugada syndrome; Congenital long QT syndrome 1 2 0 0 0 0 3
Cardiac arrest 0 0 2 1 0 0 3
Death in infancy 3 0 0 0 0 0 3
Left ventricular noncompaction cardiomyopathy 0 1 1 1 0 0 3
Sudden cardiac death 0 0 1 1 1 0 3
ATRIAL STANDSTILL 1, DIGENIC 2 0 0 0 0 0 2
Acquired long QT syndrome 0 0 0 0 0 2 2
Acute myeloid leukemia 0 0 0 0 0 2 2
Atrioventricular block 0 0 0 0 0 2 2
Brugada syndrome 1; Dilated cardiomyopathy 1E 0 1 0 0 0 1 2
Brugada syndrome 1; Long QT syndrome 3; Progressive familial heart block, type 1A; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10 0 2 0 0 0 0 2
Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1; Progressive familial heart block, type 1A; Ventricular fibrillation, paroxysmal familial, type 1; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10 0 1 1 0 0 0 2
Brugada syndrome, lidocaine-induced 0 0 1 1 0 0 2
Catecholaminergic polymorphic ventricular tachycardia 1 0 0 2 0 0 0 2
Cervical cancer 0 0 0 0 0 2 2
Conduction disorder of the heart 0 1 1 0 0 0 2
Long QT syndrome 1 1 1 0 0 0 0 2
Long QT syndrome, drug-associated 0 0 1 2 0 0 2
Long QT syndrome; Brugada syndrome 0 0 1 0 1 0 2
Melanoma 0 0 0 0 0 2 2
Ovarian serous cystadenocarcinoma 0 0 0 0 0 2 2
Sick sinus syndrome 0 1 0 0 0 1 2
Sudden cardiac arrest 0 0 2 0 0 0 2
Sudden unexplained death 0 0 1 1 0 0 2
Uterine corpus endometrial carcinoma 0 0 0 0 0 2 2
Ventricular fibrillation 0 0 0 0 0 2 2
Wolff-Parkinson-White pattern 0 2 0 0 0 0 2
AV junctional rhythm 0 0 1 0 0 0 1
Atrial fibrillation; Brugada syndrome 0 0 0 1 0 0 1
Atrial standstill 2 0 1 0 0 0 0 1
Autism 0 0 1 0 0 0 1
Branchiootic syndrome 1 1 0 0 0 0 0 1
Brugada syndrome 1; Long QT syndrome 3; Progressive familial heart block, type 1A; Ventricular fibrillation, paroxysmal familial, type 1; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10 0 1 0 0 0 0 1
Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10 0 0 0 0 0 1 1
Brugada syndrome 1; Long QT syndrome 3; Ventricular fibrillation, paroxysmal familial, type 1 0 1 0 0 0 0 1
Brugada syndrome 1; Long QT syndrome 3; Ventricular fibrillation, paroxysmal familial, type 1; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10 0 0 1 0 0 0 1
Brugada syndrome 1; SUDDEN INFANT DEATH SYNDROME 1 0 0 0 0 0 1
Brugada syndrome 1; Sick sinus syndrome 1; Dilated cardiomyopathy 1E; SUDDEN INFANT DEATH SYNDROME; Long QT syndrome 0 0 0 0 0 1 1
Brugada syndrome 1; Ventricular fibrillation, paroxysmal familial, type 1 0 0 1 0 0 0 1
CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE 1 0 0 0 0 0 1
Cardiomyopathy; Long QT syndrome 0 0 0 0 1 0 1
Congenital heart disease 0 0 0 0 1 0 1
Death in early adulthood 1 0 0 0 0 0 1
Dilated cardiomyopathy 1A 0 0 1 0 0 0 1
Familial pancreatic carcinoma 0 0 0 0 0 1 1
Familial sick sinus syndrome 0 1 0 0 0 0 1
Fetal akinesia deformation sequence 1; Arthrogryposis multiplex congenita 0 1 0 0 0 0 1
Fetal anomalies with a likely genetic cause 0 1 0 0 0 0 1
HEART BLOCK, NONPROGRESSIVE 1 0 0 0 0 0 1
Heart failure 0 0 1 0 0 0 1
Inborn genetic diseases 0 1 0 0 0 0 1
Left ventricular noncompaction 1 0 0 1 0 0 0 1
Long QT syndrome 2 0 0 1 0 0 0 1
Long QT syndrome 2/3, digenic 1 0 0 0 0 0 1
Long QT syndrome 3, acquired, susceptibility to 1 0 0 0 0 0 1
Long QT syndrome 3/6, digenic 1 0 0 0 0 0 1
Long QT syndrome 3; Dilated cardiomyopathy 1E 1 0 0 0 0 0 1
Long QT syndrome 3; Sick sinus syndrome 1; Dilated cardiomyopathy 1E; Atrial fibrillation, familial, 10; Brugada syndrome 0 0 0 0 0 1 1
Lung cancer 0 0 0 0 0 1 1
Malignant tumor of urinary bladder 0 0 0 0 0 1 1
Nonpapillary renal cell carcinoma 0 0 0 0 0 1 1
Primary dilated cardiomyopathy; Brugada syndrome 1 0 0 0 0 0 1
Primary dilated cardiomyopathy; Cardiac arrhythmia; SUDDEN INFANT DEATH SYNDROME; Long QT syndrome; Brugada syndrome; Sick sinus syndrome 0 0 0 0 0 1 1
Primary dilated cardiomyopathy; Migraine; Hemiplegia 0 0 1 0 0 0 1
Pulmonary valve stenosis (rare); Ventricular tachycardia 0 0 0 1 0 0 1
Sarcoma 0 0 0 0 0 1 1
Sinoatrial node disorder 1 0 0 0 0 0 1
Sinoatrial node disorder; Brugada syndrome; Cardiac arrest 1 0 0 0 0 0 1
Squamous cell lung carcinoma 0 0 0 0 0 1 1
Syncope 0 1 0 0 0 0 1
Thyroid cancer, nonmedullary, 1 0 0 0 0 0 1 1
Torsades de pointes 0 0 0 0 0 1 1
Unexplained death in infancy and sudden unexplained death in childhood 1 0 0 0 0 0 1
Uterine carcinosarcoma 0 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 162
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 287 68 1449 1078 76 0 2958
Color Diagnostics, LLC DBA Color Health 34 34 774 590 46 0 1478
Ambry Genetics 72 61 550 531 29 0 1243
All of Us Research Program, National Institutes of Health 27 26 697 400 25 0 1175
GeneDx 90 93 476 199 178 1 1037
Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust 0 0 0 0 0 455 455
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 25 14 113 89 41 0 282
Vandenberg Lab, The Victor Chang Cardiac Research Institute 0 0 0 0 0 265 265
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 8 17 78 61 30 0 194
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute 22 23 58 68 23 0 194
Fulgent Genetics, Fulgent Genetics 12 12 149 9 4 0 186
Illumina Laboratory Services, Illumina 2 1 139 53 43 0 174
CeGaT Center for Human Genetics Tuebingen 14 8 44 53 8 0 127
Mayo Clinic Laboratories, Mayo Clinic 7 6 51 19 27 0 110
Clinical Genetics, Academic Medical Center 11 0 20 6 70 0 107
PreventionGenetics, part of Exact Sciences 2 5 27 47 20 0 101
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 8 3 18 33 31 0 93
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 5 3 28 26 30 0 92
Roden Lab, Vanderbilt University Medical Center 0 13 34 31 0 0 78
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 2 0 11 35 18 0 66
Breakthrough Genomics, Breakthrough Genomics 0 0 4 31 30 0 65
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 20 11 31 1 0 0 63
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 5 0 11 40 4 0 60
AiLife Diagnostics, AiLife Diagnostics 4 7 46 0 0 0 57
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario 0 1 18 10 23 0 52
Genome Diagnostics Laboratory, University Medical Center Utrecht 1 3 6 27 15 0 52
MVZ Martinsried, Medicover Genetics 19 12 21 0 0 0 52
Mendelics 4 0 29 6 13 0 52
Blueprint Genetics 4 7 31 6 0 0 48
Athena Diagnostics 0 2 9 10 24 0 45
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals 2 6 25 9 3 0 45
OMIM 43 0 0 0 0 0 43
Clinical Genetics Laboratory, Skane University Hospital Lund 11 4 22 0 0 0 37
Stanford Center for Inherited Cardiovascular Disease, Stanford University 2 4 27 1 2 0 36
Revvity Omics, Revvity 3 5 27 0 0 0 35
CSER _CC_NCGL, University of Washington 0 2 24 8 0 0 34
Eurofins Ntd Llc (ga) 1 0 15 2 15 0 33
Biesecker Lab/Clinical Genomics Section, National Institutes of Health 0 1 17 8 6 0 32
Institute of Human Genetics, University of Leipzig Medical Center 3 8 9 0 2 0 22
Juno Genomics, Hangzhou Juno Genomics, Inc 5 13 4 0 0 0 22
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 4 12 2 0 1 0 18
Dr. Peter K. Rogan Lab, Western University 0 0 0 0 0 16 16
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 2 14 0 0 0 16
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 14 0 0 0 14
3billion 4 1 6 0 1 0 12
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 3 2 6 1 0 0 12
Neuberg Centre For Genomic Medicine, NCGM 0 0 12 0 0 0 12
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 5 7 0 0 0 0 12
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 3 6 2 0 0 0 11
KardioGenetik, Herz- und Diabeteszentrum NRW 2 2 7 0 0 0 11
Dasa 5 4 0 0 1 0 10
Baylor Genetics 2 1 6 0 0 0 9
Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego 1 1 2 4 1 0 9
Centre for Mendelian Genomics, University Medical Centre Ljubljana 2 3 5 0 0 0 9
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia 0 0 5 2 3 0 9
New York Genome Center 1 1 7 0 0 0 9
Cohesion Phenomics 0 0 0 0 8 0 8
GenomeConnect, ClinGen 0 0 0 0 0 8 8
Institute of Immunology and Genetics Kaiserslautern 1 4 3 0 0 0 8
Molecular Genetics, Royal Melbourne Hospital 0 1 7 0 0 0 8
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 4 3 0 0 0 0 7
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine 6 0 0 0 0 0 6
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 1 3 2 0 0 0 6
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 4 0 2 0 6
Genetics and Molecular Pathology, SA Pathology 2 3 1 0 0 0 6
ISCA Site 6 0 0 0 3 3 0 6
Center for Medical Genetics Ghent, University of Ghent 0 5 0 0 0 0 5
Clinical Genomics Laboratory, Stanford Medicine 1 0 4 0 0 0 5
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 2 1 1 0 1 0 5
Genetics and Genomics Program, Sidra Medicine 0 1 4 0 0 0 5
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 5 5
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 2 3 0 0 0 0 5
MGZ Medical Genetics Center 0 2 3 0 0 0 5
Robert's Program, Boston Children's Hospital 1 1 3 0 0 0 5
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 1 0 0 2 1 0 4
Division of Human Genetics, Children's Hospital of Philadelphia 2 0 2 0 0 0 4
GeneReviews 0 0 0 0 0 4 4
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 2 1 0 0 0 4
Institute of Human Genetics, Heidelberg University 3 1 0 0 0 0 4
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 1 3 0 0 0 4
Phosphorus, Inc. 0 0 3 1 0 0 4
Center for Human Genetics, University of Leuven 0 0 3 0 0 0 3
Dept of Medical Biology, Uskudar University 2 0 1 0 0 0 3
Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences 3 0 0 0 0 0 3
Institute of Human Genetics Munich, TUM University Hospital 1 2 0 0 0 0 3
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 0 1 2 0 0 0 3
Lildballe Lab, Aarhus University Hospital 0 2 0 1 0 0 3
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 0 0 2 0 0 0 2
CENTOGENE GmbH and LLC - Guiding Precision Medicine 0 1 1 0 0 0 2
Center for Human Genetics and Genomic Medicine, Uniklinik Rwth Aachen 1 1 0 0 0 0 2
Centre of Medical Genetics, University of Antwerp 1 1 0 0 0 0 2
Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University 0 0 2 0 0 0 2
Clinical Genetics Laboratory, Region Ostergotland 0 2 0 0 0 0 2
Clinical Genetics and Genomics, Karolinska University Hospital 0 2 0 0 0 0 2
Clinical Genomics Laboratory, Washington University in St. Louis 1 1 0 0 0 0 2
Department of Genetics and Molecular Biology, Isfahan University of Medical Sciences 0 2 0 0 0 0 2
Department of Traditional Chinese Medicine, Fujian Provincial Hospital 1 0 1 0 0 0 2
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ 0 0 2 0 0 0 2
Genomics England Pilot Project, Genomics England 1 1 0 0 0 0 2
Gharavi Laboratory, Columbia University 1 1 0 0 0 0 2
Human Genetics Bochum, Ruhr University Bochum 1 1 0 0 0 0 2
Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital 2 0 0 0 0 0 2
Johns Hopkins Genomics, Johns Hopkins University 1 0 1 0 0 0 2
Klaassen Lab, Charite University Medicine Berlin 0 0 2 0 0 0 2
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 0 0 0 1 1 0 2
Laboratory of Genetics and Molecular Cardiology, University of São Paulo 0 0 2 0 0 0 2
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 2 0 0 0 0 2
Medical Genetics Clinic, University of Catania 0 1 1 0 0 0 2
North West Genomic Laboratory Hub, Manchester University NHS Foundation Trust 1 1 0 0 0 0 2
OLLIN Analises Genomicas, OLLIN 1 1 0 0 0 0 2
Research Unit of Cardiovascular and Metabolic Disease, Inserm 0 2 0 0 0 0 2
SIB Swiss Institute of Bioinformatics 0 1 1 0 0 0 2
UCLA Clinical Genomics Center, UCLA 0 2 0 0 0 0 2
deCODE genetics, Amgen 0 2 0 0 0 0 2
Beijing Key Laboratry for Genetics of Birth Defects, Beijing Children's Hospital 0 1 0 0 0 0 1
Biology Molecular and Stem Cell Facilities Laboratory, National Cardiovascular Center, Harapan Kita Hospital 1 0 0 0 0 0 1
Breda Genetics srl, Breda Genetics srl 0 0 1 0 0 0 1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 0 1 0 0 0 1
Cambridge Genomics Laboratory, East Genomic Laboratory Hub, NHS Genomic Medicine Service 0 0 1 0 0 0 1
Cardiac Research Department, West China Second University Hospital 1 0 0 0 0 0 1
Cardiology unit, Meyer University Hospital 0 0 1 0 0 0 1
Cardiovascular Center, Jinshazhou Hospital of Guangzhou University of Chinese Medicine 1 0 0 0 0 0 1
Center for Human Genetics, Inc, Center for Human Genetics, Inc 1 0 0 0 0 0 1
Center for Molecular Medicine, Children’s Hospital of Fudan University 1 0 0 0 0 0 1
Center for Personalized Medicine, Children's Hospital Los Angeles 0 0 1 0 0 0 1
Centre for Addiction & Mental Health, Centre for Addiction & Mental Health 0 0 1 0 0 0 1
Cirak Lab, University Hospital Cologne 0 1 0 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 1 0 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 0 0 1 0 0 0 1
Department of Human Genetics, Hannover Medical School 0 1 0 0 0 0 1
Diagnostics Centre, Carl Von Ossietzky University Oldenburg 0 1 0 0 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 0 0 0 1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center 0 1 0 0 0 0 1
Donald Williams Parsons Laboratory, Baylor College of Medicine 1 0 0 0 0 0 1
Dubai Health Genomic Medicine Center, Dubai Health 0 0 0 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 1 0 0 0 0 1
GOSgene, University College London Great Ormond Street Institute of Child Health 0 1 0 0 0 0 1
Gemeinschaftspraxis fuer Humangenetik Dresden 1 0 0 0 0 0 1
GeneID Lab - Advanced Molecular Diagnostics 0 1 0 0 0 0 1
Genesis Genoma Lab, Genesis Genoma Lab 0 1 0 0 0 0 1
Genesolutions, Medical Genetics Institutes, Ho Chi Minh City, Vietnam 0 1 0 0 0 0 1
Genetic Services Laboratory, University of Chicago 0 0 1 0 0 0 1
Genetics Laboratory, Great Ormond Street Hospital NHS Foundation Trust, North Thames Genomic Laboratory Hub 0 1 0 0 0 0 1
GenomeConnect - Brain Gene Registry 0 0 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 1 0 0 1 0 0 1
ITMI 0 0 1 0 0 0 1
Institute for Genetics of Heart Diseases, University Hospital Muenster 0 1 0 0 0 0 1
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 0 1 0 0 0 0 1
Institute of Human Genetics, University of Goettingen 0 0 1 0 0 0 1
Institute of Human Genetics, University of Wuerzburg 0 1 0 0 0 0 1
Laan Lab, Human Genetics Research Group, University of Tartu 0 1 0 0 0 0 1
Laboratory of Genetics, Children's Clinical University Hospital Latvia 0 0 0 1 0 0 1
Medical Research Institute, Tokyo Medical and Dental University 0 1 0 0 0 0 1
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology 0 1 0 0 0 0 1
Molecular Genetics Laboratory, Motol Hospital 0 1 0 0 0 0 1
Muscat Medical Center, Bion Medical Genetic Lab 1 0 0 0 0 0 1
National Institute of Allergy and Infectious Diseases - Centralized Sequencing Program, National Institutes of Health 0 0 1 0 0 0 1
Pediatrics, West China Second University Hospital, Sichuan University 0 1 0 0 0 0 1
Provincial Medical Genetics Program of British Columbia, University of British Columbia 0 0 1 0 0 0 1
Servicio Canario de Salud, Hospital Universitario Nuestra Sra. de Candelaria 0 1 0 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 0 0 1
University of Washington Department of Laboratory Medicine, University of Washington 0 0 1 0 0 0 1

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