ClinVar Miner

Variants in gene LMNA

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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
413 348 1039 609 94 301 2169

Condition and significance breakdown #

Total conditions: 121
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Charcot-Marie-Tooth disease type 2 300 120 553 449 20 0 1442
not provided 113 96 345 91 64 255 765
Cardiovascular phenotype 73 36 220 186 4 0 516
Cardiomyopathy 10 17 265 194 18 0 494
Primary dilated cardiomyopathy 22 34 255 120 11 0 433
not specified 0 2 90 91 45 1 203
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Mandibuloacral dysplasia with type A lipodystrophy; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive; Restrictive dermopathy 2 10 11 125 20 1 0 167
Dilated cardiomyopathy 1A 47 41 59 10 4 6 148
Emery-Dreifuss muscular dystrophy 2, autosomal dominant 20 12 31 8 9 2 80
Congenital muscular dystrophy due to LMNA mutation 11 8 45 8 6 1 77
Familial partial lipodystrophy, Dunnigan type 16 9 31 5 12 0 71
Charcot-Marie-Tooth disease 2 3 22 25 7 0 58
LMNA-related disorder 13 5 17 19 1 0 55
Hutchinson-Gilford syndrome 7 11 17 0 5 17 49
Charcot-Marie-Tooth disease type 2B1 3 2 26 8 9 0 47
Mandibuloacral dysplasia with type A lipodystrophy 6 2 26 8 6 0 46
Lethal tight skin contracture syndrome 0 0 28 8 6 0 42
Emery-Dreifuss muscular dystrophy 1 0 22 5 12 0 40
Lipoatrophy with Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy, and Leukomelanodermic Papules 0 0 26 8 6 0 40
Primary familial dilated cardiomyopathy 11 4 2 0 0 0 17
Muscular dystrophy 9 3 0 0 0 0 12
Ovarian serous cystadenocarcinoma 0 0 0 0 0 11 11
Laminopathy 3 2 2 0 0 0 7
Thyroid cancer, nonmedullary, 1 0 0 0 0 0 7 7
Abnormality of the musculature 2 4 0 0 0 0 6
Monogenic diabetes 1 1 2 1 1 0 6
Congenital muscular dystrophy 2 2 0 1 0 0 5
Emery-Dreifuss muscular dystrophy 3, autosomal recessive 3 0 2 0 0 0 5
Heart-hand syndrome, Slovenian type 2 2 1 0 0 0 5
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome 2 0 2 0 0 0 4
Mandibuloacral dysplasia with type A lipodystrophy, atypical 4 0 0 0 0 0 4
Melanoma 0 0 0 0 0 4 4
Primary familial hypertrophic cardiomyopathy 0 1 3 0 0 0 4
Arrhythmogenic right ventricular cardiomyopathy 1 1 1 0 0 0 3
Cervical cancer 0 0 0 0 0 3 3
Charcot-Marie-Tooth disease type 2B1; Mandibuloacral dysplasia with type A lipodystrophy; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 3 0 0 0 0 3
Dilated cardiomyopathy 1S 2 1 0 0 0 0 3
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Mandibuloacral dysplasia with type A lipodystrophy; Lethal tight skin contracture syndrome; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 1 0 2 0 0 0 3
Familial cancer of breast 0 0 0 0 0 3 3
Hepatocellular carcinoma 0 0 0 0 0 3 3
Hutchinson-Gilford progeria syndrome, atypical 3 0 0 0 0 0 3
Lung cancer 0 0 0 0 0 3 3
Mandibuloacral dysplasia 1 2 1 0 0 0 3
Arrhythmogenic right ventricular dysplasia 9 0 2 0 0 0 0 2
Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 2 0 0 0 2
Cholangiocarcinoma 0 0 0 0 0 2 2
Dilated and arrhythmogenic cardiomyopathy 0 2 0 0 0 0 2
Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 0 0 0 2 2
Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Mandibuloacral dysplasia with type A lipodystrophy; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 0 0 0 2 2
Familial pancreatic carcinoma 0 0 0 0 0 2 2
Familial partial lipodystrophy 1 0 0 0 1 0 2
Gastric cancer 0 0 0 0 0 2 2
Hypertrophic cardiomyopathy 0 0 2 0 0 0 2
Left ventricular noncompaction 1 1 0 0 0 0 2
Lipodystrophy 0 1 1 0 0 0 2
Malignant tumor of urinary bladder 0 0 0 0 0 2 2
Nonpapillary renal cell carcinoma 0 0 0 0 0 2 2
Primary dilated cardiomyopathy; Laminopathy 1 1 0 0 0 0 2
Restrictive dermopathy 2 2 0 0 0 0 0 2
See cases 2 0 0 0 0 0 2
Thymoma 0 0 0 0 0 2 2
Uterine carcinosarcoma 0 0 0 0 0 2 2
Uterine corpus endometrial carcinoma 0 0 0 0 0 2 2
Uveal melanoma 0 0 0 0 0 2 2
Autosomal recessive axonal hereditary motor and sensory neuropathy 1 0 0 0 0 0 1
Autosomal recessive limb-girdle muscular dystrophy type 2B 1 0 0 0 0 0 1
Autosomal semi-dominant severe lipodystrophic laminopathy 0 0 1 0 0 0 1
Bethlem myopathy 1A 0 1 0 0 0 0 1
Catecholaminergic polymorphic ventricular tachycardia 1 0 0 1 0 0 0 1
Collapse (finding); Family history of sudden cardiac death 0 0 1 0 0 0 1
Colon adenocarcinoma 0 0 0 0 0 1 1
Conduction system disorder 0 1 0 0 0 0 1
Dehydrated hereditary stomatocytosis 2 0 1 0 0 0 0 1
Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Congenital muscular dystrophy due to LMNA mutation 0 0 0 0 0 1 1
Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 0 0 0 1 1
Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant 0 0 1 0 0 0 1
Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Congenital muscular dystrophy due to LMNA mutation 1 0 0 0 0 0 1
Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 1 0 0 0 1
Dilated cardiomyopathy 1A; Familial partial lipodystrophy, Dunnigan type 0 0 1 0 0 0 1
Dilated cardiomyopathy 1A; Restrictive dermopathy 2 0 0 1 0 0 0 1
Dilated cardiomyopathy 1D 0 1 0 0 0 0 1
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive; Mandibuloacral dysplasia; Laminopathy; Restrictive dermopathy 2 0 0 1 0 0 0 1
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Mandibuloacral dysplasia with type A lipodystrophy; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive; Laminopathy; Restrictive dermopathy 2 0 0 1 0 0 0 1
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Familial partial lipodystrophy, Dunnigan type 0 0 1 0 0 0 1
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Familial partial lipodystrophy, Dunnigan type; Mandibuloacral dysplasia with type A lipodystrophy 0 1 0 0 0 0 1
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome; Dilated cardiomyopathy 1A; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation 0 1 0 0 0 0 1
Early onset multivalvular disease 0 1 0 0 0 0 1
Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Congenital muscular dystrophy due to LMNA mutation 1 0 0 0 0 0 1
Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 1 0 0 0 1
Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Heart-hand syndrome, Slovenian type; Mandibuloacral dysplasia with type A lipodystrophy; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 1 0 0 0 1
Hereditary liability to pressure palsies 0 0 1 0 0 0 1
Hutchinson-Gilford progeria syndrome, childhood-onset; Right ventricular cardiomyopathy 1 0 0 0 0 0 1
Hypertrophic cardiomyopathy 1 1 0 0 0 0 0 1
Inborn genetic diseases 1 0 0 0 0 0 1
Insulin-resistant diabetes mellitus AND acanthosis nigricans 0 0 1 0 0 0 1
Intellectual disability 0 0 1 0 0 0 1
LMNA-associated condition 0 1 0 0 0 0 1
Limb-girdle muscular dystrophy 0 1 0 0 0 0 1
Lipodystrophy - childhood onset 1 0 0 0 0 0 1
Long QT syndrome 0 0 0 0 1 0 1
Malignant tumor of esophagus 0 0 0 0 0 1 1
Maturity-onset diabetes of the young 0 0 0 1 0 0 1
Metabolic disease 0 0 1 0 0 0 1
Neuromuscular disease 1 0 0 0 0 0 1
Neuronopathy, distal hereditary motor, autosomal dominant 0 0 1 0 0 0 1
Papillary renal cell carcinoma type 1 0 0 0 0 0 1 1
Peripheral neuropathy 0 0 1 0 0 0 1
Polyneuropathy 0 0 1 0 0 0 1
Primary dilated cardiomyopathy; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Familial partial lipodystrophy, Dunnigan type; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive 0 0 0 0 0 1 1
Primary dilated cardiomyopathy; Hutchinson-Gilford syndrome 1 0 0 0 0 0 1
Primary dilated cardiomyopathy; Myocarditis 0 1 0 0 0 0 1
Primary dilated cardiomyopathy; Neuromuscular disease 0 1 0 0 0 0 1
Primary familial dilated cardiomyopathy; Peripheral neuropathy 0 1 0 0 0 0 1
Proximal muscle weakness 0 1 0 0 0 0 1
Sarcoma 0 0 0 0 0 1 1
Short stature; Microtia; Microretrognathia; 2-3 finger cutaneous syndactyly; Hypercholesterolemia; Decreased body weight; Round ear 1 0 0 0 0 0 1
Sick sinus syndrome 0 1 0 0 0 0 1
Sudden unexplained death 1 0 0 0 0 0 1
Variant of unknown significance 0 0 1 0 0 0 1
Ventricular tachycardia 0 1 0 0 0 0 1
Wolff-Parkinson-White pattern 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 150
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 300 120 553 450 20 0 1443
Ambry Genetics 69 29 207 186 4 0 495
Color Diagnostics, LLC DBA Color Health 7 4 249 193 13 0 466
GeneDx 82 50 152 63 72 0 419
All of Us Research Program, National Institutes of Health 5 6 244 119 6 0 380
Epithelial Biology; Institute of Medical Biology, Singapore 0 0 0 0 0 253 253
Fulgent Genetics, Fulgent Genetics 11 11 123 20 1 0 166
Eurofins Ntd Llc (ga) 24 5 116 7 8 0 160
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 18 28 43 29 9 1 128
Revvity Omics, Revvity 19 10 92 3 0 0 124
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 16 11 37 25 12 0 100
CeGaT Center for Human Genetics Tuebingen 13 8 45 32 0 0 98
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute 13 12 27 14 12 0 78
Athena Diagnostics 9 6 30 6 12 0 63
PreventionGenetics, part of Exact Sciences 8 4 15 27 8 0 62
Molecular Genetics Laboratory, London Health Sciences Centre 2 2 19 25 7 0 55
Genetic Services Laboratory, University of Chicago 23 9 11 7 4 0 54
Mayo Clinic Laboratories, Mayo Clinic 11 5 23 9 5 0 53
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario 3 8 24 7 9 0 51
OMIM 48 0 1 0 0 0 49
Clinical Genetics, Academic Medical Center 7 2 10 2 23 0 44
Illumina Laboratory Services, Illumina 3 1 28 13 12 0 44
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 5 4 14 11 10 0 44
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 3 2 13 13 12 0 43
Breakthrough Genomics, Breakthrough Genomics 0 0 2 10 30 0 42
Dr. Peter K. Rogan Lab, Western University 0 0 0 0 0 38 38
Genome Diagnostics Laboratory, University Medical Center Utrecht 5 5 5 12 10 0 37
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 16 4 10 0 0 0 30
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 2 3 7 8 7 0 27
GeneReviews 0 0 0 0 0 25 25
Blueprint Genetics 5 11 8 0 0 0 24
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 3 0 7 6 8 0 24
3billion 10 6 7 0 0 0 23
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 2 1 5 12 2 0 22
Clinical Genetics Laboratory, Skane University Hospital Lund 8 4 5 0 0 0 17
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 6 4 8 0 0 0 17
Stanford Center for Inherited Cardiovascular Disease, Stanford University 5 6 6 0 0 0 17
Baylor Genetics 3 1 12 0 0 0 16
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic 0 3 7 3 2 0 15
Institute of Human Genetics, University of Leipzig Medical Center 5 5 5 0 0 0 14
Kariminejad - Najmabadi Pathology & Genetics Center 2 6 6 0 0 0 14
AiLife Diagnostics, AiLife Diagnostics 3 3 7 0 0 0 13
CSER _CC_NCGL, University of Washington 1 0 10 1 0 0 12
New York Genome Center 2 1 9 0 0 0 12
Centre for Mendelian Genomics, University Medical Centre Ljubljana 3 1 6 0 0 0 10
Sangiuolo Lab - Medical Genetics Laboratory, Tor Vergata University 3 6 1 0 0 0 10
Mendelics 2 4 2 0 1 0 9
Biesecker Lab/Clinical Genomics Section, National Institutes of Health 0 0 3 1 3 0 7
Dasa 5 2 0 0 0 0 7
Genomic Research Center, Shahid Beheshti University of Medical Sciences 2 2 2 0 1 0 7
Juno Genomics, Hangzhou Juno Genomics, Inc 3 4 0 0 0 0 7
MGZ Medical Genetics Center 0 5 2 0 0 0 7
Molecular Genetics, Royal Melbourne Hospital 2 2 2 1 0 0 7
Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego 2 1 1 1 1 0 6
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 2 2 2 0 0 0 6
Inherited Neuropathy Consortium 0 0 6 0 0 0 6
Institute of Human Genetics, University of Wuerzburg 0 2 4 0 0 0 6
Neuberg Centre For Genomic Medicine, NCGM 4 1 1 0 0 0 6
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 1 3 2 0 0 0 6
Cohesion Phenomics 0 0 0 0 5 0 5
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 5 5
Institute of Immunology and Genetics Kaiserslautern 2 0 3 0 0 0 5
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 2 2 1 0 0 0 5
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 4 1 0 0 0 0 5
University of Washington Center for Mendelian Genomics, University of Washington 0 0 5 0 0 0 5
Variantyx, Inc. 3 2 0 0 0 0 5
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 1 0 2 0 1 0 4
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 1 0 2 0 1 0 4
Clinical Center for Gene Diagnosis and Therapy, Department of Cardiovascular Surgery, The Second Xiangya Hospital of Central South University 2 1 1 0 0 0 4
Clinical Genomics Laboratory, Stanford Medicine 0 0 4 0 0 0 4
GenomeConnect, ClinGen 0 0 0 0 0 4 4
Institut für Laboratoriums- und Transfusionsmedizin, Herz- und Diabeteszentrum Nordrhein-Westfalen 2 2 0 0 0 0 4
Institute Of Molecular Biology And Genetics, Federal Almazov National Medical Research Centre 1 2 1 0 0 0 4
Johns Hopkins Genomics, Johns Hopkins University 2 1 1 0 0 0 4
Laboratory of Genetics, Children's Clinical University Hospital Latvia 2 0 0 2 0 0 4
Personalized Diabetes Medicine Program, University of Maryland School of Medicine 0 0 2 1 1 0 4
School of Medicine, Universitat de Girona 0 0 4 0 0 0 4
Cambridge Genomics Laboratory, East Genomic Laboratory Hub, NHS Genomic Medicine Service 1 1 1 0 0 0 3
Department of Pathology and Laboratory Medicine, Sinai Health System 0 1 2 0 0 0 3
Dubai Health Genomic Medicine Center, Dubai Health 1 1 1 0 0 0 3
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 1 2 0 0 0 3
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 1 2 0 0 0 0 3
Institute of Human Genetics Munich, TUM University Hospital 0 3 0 0 0 0 3
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 3 0 0 0 0 0 3
MVZ Martinsried, Medicover Genetics 1 2 0 0 0 0 3
Phosphorus, Inc. 0 0 3 0 0 0 3
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute 1 0 1 0 0 0 2
Center for Genetic Medicine Research, Children's National Medical Center 0 1 1 0 0 0 2
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 2 0 0 0 2
Center for Human Genetics, University of Leuven 0 1 1 0 0 0 2
Center of Excellence for Medical Genomics, Chulalongkorn University 2 0 0 0 0 0 2
Centre of Medical Genetics, University Hospital Muenster 1 1 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 0 1 0 0 0 2
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 0 2 0 0 0 0 2
Department of Human Genetics, Hannover Medical School 1 1 0 0 0 0 2
Department of Medical Genetics, National Institute of Health 2 0 0 0 0 0 2
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences 0 2 0 0 0 0 2
Department of Rehabilitation Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea 1 0 1 0 0 0 2
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 2 0 0 0 2
First Genomix Gene Laboratory, Genetic Diagnostics Department 0 2 0 0 0 0 2
Genetics and Molecular Pathology, SA Pathology 0 2 0 0 0 0 2
Gharavi Laboratory, Columbia University 1 0 1 0 0 0 2
Human Genetics Bochum, Ruhr University Bochum 1 0 1 0 0 0 2
Institute of Human Genetics, University of Goettingen 0 2 0 0 0 0 2
KTest Genetics, KTest 1 1 0 0 0 0 2
Klaassen Lab, Charite University Medicine Berlin 0 1 1 0 0 0 2
Loeys Lab, Universiteit Antwerpen 1 0 1 0 0 0 2
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 0 2 0 0 0 2
Molecular Genetics Laboratory, Motol Hospital 2 0 0 0 0 0 2
North West Genomic Laboratory Hub, Manchester University NHS Foundation Trust 0 2 0 0 0 0 2
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 2 0 0 0 0 0 2
Rajaie Cardiovascular, Medical and Research Center, Iran University of Medical Sciences 1 1 0 0 0 0 2
Solve-RD Consortium 0 2 0 0 0 0 2
Suma Genomics 0 2 0 0 0 0 2
Translational Genomics Laboratory, University of Maryland School of Medicine 1 1 0 0 0 0 2
Undiagnosed Diseases Network, NIH 0 2 0 0 0 0 2
Andelfinger Lab, Centre de Recherche, CHU Sainte Justine 1 0 0 0 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 1 0 0 0 0 0 1
Center for Human Genetics and Genomic Medicine, Uniklinik Rwth Aachen 0 0 1 0 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 0 0 0 0 1
Claritas Genomics 0 0 1 0 0 0 1
Clinical Biomedical Laboratory, Shriners Hospital For Children - Canada 0 1 0 0 0 0 1
Clinical Genetics Laboratory, Region Ostergotland 1 0 0 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 0 1 0 0 0 0 1
Clinical Omics and Informatics (COIN) Unit, Neuroscience Institute, University Of Cape Town 0 1 0 0 0 0 1
Department of Cardiovascular Medicine, The University of Tokyo, Graduate School of Medicine 0 1 0 0 0 0 1
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 0 1 0 0 0 0 1
Dept. of Medical Genetics, Telemark Hospital Trust, Telemark Hospital Trust 0 1 0 0 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 0 0 0 1
Eurofins-Biomnis 1 0 0 0 0 0 1
Genome Diagnostics Laboratory, Amsterdam University Medical Center 0 0 1 0 0 0 1
Genomics of Heart & Lung Disease, Institut Universitaire de Cardiologie Et de Pneumologie de Québec - Université Laval 0 1 0 0 0 0 1
HUSP Clinical Genetics Laboratory, Hospital Universitario San Pedro De Logroño (HUSP) 0 0 1 0 0 0 1
Imagene.me medical diagnostic laboratory, IMAGENE.ME SA 1 0 0 0 0 0 1
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden 1 0 0 0 0 0 1
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 1 0 0 0 0 0 1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 0 0 0 0 0 1
Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg 1 0 0 0 0 0 1
KardioGenetik, Herz- und Diabeteszentrum NRW 0 0 1 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 0 1
Laan Lab, Human Genetics Research Group, University of Tartu 0 1 0 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 1 0 0 0 0 0 1
Laboratory of Medical Genetics, Tor Vergata University 1 0 0 0 0 0 1
Laboratório de Neurologia Aplicada e Experimental, Faculdade de Medicina de Ribeirao Preto – Universidade de Sao Paulo 0 0 1 0 0 0 1
Narges Medical Genetic and Prenatal Diagnosis Lab 0 1 0 0 0 0 1
SIB Swiss Institute of Bioinformatics 0 1 0 0 0 0 1
SNPedia 0 0 0 0 0 1 1
Service of Pediatric Gastrohepatology and Metabolic Diseases, University of Medicine of Tirana 0 1 0 0 0 0 1
UCLA Clinical Genomics Center, UCLA 1 0 0 0 0 0 1

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