ClinVar Miner

Variants in gene COL2A1

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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
732 532 1112 1314 303 25 3527

Condition and significance breakdown #

Total conditions: 83
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
not provided 580 334 911 1275 266 1 3112
Stickler syndrome type 1 77 49 92 26 33 2 272
COL2A1-related disorder 26 37 51 67 2 1 183
not specified 2 7 12 76 78 0 163
Inborn genetic diseases 12 9 123 10 0 0 154
Type 2 collagenopathy 17 7 38 14 69 1 146
Connective tissue disorder 5 14 13 24 17 0 72
Spondyloepiphyseal dysplasia congenita 30 17 5 0 0 0 50
Achondrogenesis type II 18 22 8 1 0 0 49
Spondyloperipheral dysplasia 13 14 8 0 0 0 35
Stickler syndrome 26 5 1 0 0 0 32
Stickler syndrome, type I, nonsyndromic ocular 13 8 10 0 0 0 30
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Multiple epiphyseal dysplasia, Beighton type; Legg-Calve-Perthes disease; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Stickler syndrome, type I, nonsyndromic ocular; Vitreoretinopathy with phalangeal epiphyseal dysplasia; Spondyloepiphyseal dysplasia, Stanescu type; Spondyloepimetaphyseal dysplasia, Strudwick type 9 8 9 0 0 0 26
Kniest dysplasia 14 7 3 0 0 0 24
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Multiple epiphyseal dysplasia, Beighton type; Legg-Calve-Perthes disease; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondylometaphyseal dysplasia - Sutcliffe type; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Stickler syndrome, type I, nonsyndromic ocular; Vitreoretinopathy with phalangeal epiphyseal dysplasia; Spondyloepiphyseal dysplasia, Stanescu type; Spondyloepimetaphyseal dysplasia, Strudwick type 2 0 6 11 3 0 22
Spondyloepimetaphyseal dysplasia, Strudwick type 11 7 0 0 0 0 17
Spondyloepiphyseal dysplasia, Stanescu type 5 3 4 0 1 0 13
Retinal dystrophy 3 3 6 0 0 0 12
Autosomal dominant COL2A1-related disorders 4 6 0 0 0 0 10
Platyspondylic dysplasia, Torrance type 3 5 0 0 0 1 9
Avascular necrosis of femoral head, primary, 1 3 3 1 0 0 0 6
See cases 2 4 0 0 0 0 6
Multiple epiphyseal dysplasia, Beighton type 3 1 1 0 0 0 5
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Multiple epiphyseal dysplasia, Beighton type; Legg-Calve-Perthes disease; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondylometaphyseal dysplasia; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Stickler syndrome, type I, nonsyndromic ocular; Spondyloepiphyseal dysplasia, Stanescu type 3 0 1 0 0 0 4
COL2A1-related skeletal dysplasia 2 1 0 0 0 1 4
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Multiple epiphyseal dysplasia, Beighton type; Legg-Calve-Perthes disease; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondylometaphyseal dysplasia, Schmidt type; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Stickler syndrome, type I, nonsyndromic ocular; Vitreoretinopathy with phalangeal epiphyseal dysplasia; Spondyloepiphyseal dysplasia, Stanescu type; Spondyloepimetaphyseal dysplasia, Strudwick type 0 3 0 0 0 0 3
Hypochondrogenesis 3 0 0 0 0 0 3
MASS syndrome 0 2 1 0 0 0 3
Spondyloepiphyseal dysplasia with metatarsal shortening 2 1 0 0 0 0 3
Spondylometaphyseal dysplasia - Sutcliffe type 0 0 0 0 0 3 3
Achondrogenesis type II; Kniest dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Hypochondrogenesis; Spondyloepimetaphyseal dysplasia, Strudwick type 0 0 0 0 0 2 2
Autosomal dominant rhegmatogenous retinal detachment 2 0 0 0 0 0 2
Cervical cancer 0 0 0 0 0 2 2
Fetal anomalies with a likely genetic cause 0 1 1 0 0 0 2
Hearing impairment 0 0 1 0 1 0 2
Intellectual disability 0 0 0 2 0 0 2
Legg-Calve-Perthes disease 1 1 0 0 0 0 2
Melanoma 0 0 0 0 0 2 2
Namaqualand hip dysplasia 2 0 0 0 0 0 2
Otospondylomegaepiphyseal dysplasia, autosomal dominant 2 0 0 0 0 0 2
Otospondylomegaepiphyseal dysplasia, autosomal recessive 1 0 1 0 0 0 2
Ovarian serous cystadenocarcinoma 0 0 0 0 0 2 2
Spondylometaphyseal dysplasia 0 0 2 0 0 0 2
Spondylometaphyseal dysplasia, Schmidt type 2 0 0 0 0 0 2
Thymoma 0 0 0 0 0 2 2
Uterine corpus endometrial carcinoma 0 0 0 0 0 2 2
Abnormal cartilage collagen 0 0 1 0 0 0 1
Abnormality of the skeletal system 0 1 0 0 0 0 1
Acetabular dysplasia 1 0 0 0 0 0 1
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Legg-Calve-Perthes disease; Kniest dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondyloepiphyseal dysplasia with metatarsal shortening; Spondyloepiphyseal dysplasia, Stanescu type 0 0 0 0 0 1 1
Achondrogenesis type II; Avascular necrosis of femoral head, primary, 1; Multiple epiphyseal dysplasia, Beighton type; Legg-Calve-Perthes disease; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondylometaphyseal dysplasia; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Stickler syndrome, type I, nonsyndromic ocular; Epiphyseal dysplasia, multiple, 6; Stickler syndrome, type 4; Spondyloepiphyseal dysplasia, Stanescu type 0 0 1 0 0 0 1
Achondrogenesis type II; Kniest dysplasia; Namaqualand hip dysplasia; Spondyloperipheral dysplasia; Platyspondylic dysplasia, Torrance type; Spondyloepimetaphyseal dysplasia, Strudwick type 0 1 0 0 0 0 1
Achondrogenesis type II; Kniest dysplasia; Stickler syndrome type 1; Platyspondylic dysplasia, Torrance type; Spondyloepiphyseal dysplasia congenita; Spondyloepiphyseal dysplasia with metatarsal shortening; Osteoarthritis; Spondyloepimetaphyseal dysplasia, Strudwick type 0 0 0 0 0 1 1
COL2A1-related phenotype 0 1 0 0 0 0 1
COL2A1-related skeletal disorder 1 0 0 0 0 0 1
Congenital aneurysm of ascending aorta 0 0 1 0 0 0 1
EBV-positive nodal T- and NK-cell lymphoma 0 0 0 1 0 0 1
Gastric cancer 0 0 0 0 0 1 1
Heart, malformation of; Micrognathia 1 0 0 0 0 0 1
Hereditary breast ovarian cancer syndrome 0 0 1 0 0 0 1
KBG syndrome 0 1 0 0 0 0 1
Kniest dysplasia; Spondyloepimetaphyseal dysplasia, Strudwick type 0 1 0 0 0 0 1
Maffucci syndrome 0 1 0 0 0 0 1
Marfan syndrome 0 1 0 0 0 0 1
Mendelian syndromes with cleft lip/palate 0 0 1 0 0 0 1
Monogenic hearing loss 0 0 1 0 0 0 1
Myopia 1 0 0 0 0 0 1
Narrow chest; Disproportionate short-limb short stature 0 1 0 0 0 0 1
Optic atrophy 0 0 1 0 0 0 1
Orofacial cleft 1 0 0 1 0 0 0 1
Paediatric disorders 1 0 0 0 0 0 1
Retinal detachment 1 0 0 0 0 0 1
Retinitis pigmentosa 0 0 1 0 0 0 1
Short ribs; Absent vertebral body mineralization 1 0 0 0 0 0 1
Short stature 0 1 0 0 0 0 1
Short stature; Hearing impairment; Developmental dysplasia of the hip; Scoliosis; Multiple epiphyseal dysplasia; Hypoplastic acetabulae 0 1 0 0 0 0 1
Skeletal dysplasia 0 1 0 0 0 0 1
Spondyloepiphyseal dysplasia 0 1 0 0 0 0 1
Spondyloepiphyseal dysplasia, Namaqualand type 0 1 0 0 0 0 1
Stargardt disease 1 0 0 0 0 0 1
Stickler syndrome type 1; Stickler syndrome, type I, nonsyndromic ocular 1 0 0 0 0 0 1
Uveal melanoma 0 0 0 0 0 1 1
Vitreoretinopathy with phalangeal epiphyseal dysplasia 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 152
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 457 238 645 1185 139 0 2664
GeneDx 171 38 278 161 166 0 814
PreventionGenetics, part of Exact Sciences 17 26 41 80 37 0 201
Ambry Genetics 12 9 123 10 0 0 154
Illumina Laboratory Services, Illumina 7 3 75 36 71 0 134
Breakthrough Genomics, Breakthrough Genomics 0 0 5 22 94 0 121
Eurofins Ntd Llc (ga) 35 16 46 6 18 0 121
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 7 20 8 28 38 0 101
CeGaT Center for Human Genetics Tuebingen 12 10 25 40 10 0 97
3billion 24 19 19 0 0 0 62
OMIM 57 0 0 0 0 0 57
Genome Diagnostics Laboratory, The Hospital for Sick Children 5 13 8 8 17 0 51
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 5 6 6 21 12 0 50
Blueprint Genetics 10 24 7 0 0 0 41
Fulgent Genetics, Fulgent Genetics 8 4 12 11 3 0 38
Center for Human Genetics, Inc, Center for Human Genetics, Inc 5 5 6 19 0 0 35
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 8 0 3 2 21 0 34
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 23 7 4 0 0 0 34
Revvity Omics, Revvity 5 8 20 0 0 0 33
Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics 20 8 1 0 0 0 29
Genome Diagnostics Laboratory, Amsterdam University Medical Center 1 0 0 0 27 0 28
Mendelics 12 10 2 0 3 0 27
Cambridge Genomics Laboratory, East Genomic Laboratory Hub, NHS Genomic Medicine Service 22 2 1 0 0 0 25
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 4 0 1 12 7 0 24
Juno Genomics, Hangzhou Juno Genomics, Inc 11 8 5 0 0 0 24
Clinical Genetics and Genomics, Karolinska University Hospital 10 9 1 0 0 0 20
Mayo Clinic Laboratories, Mayo Clinic 1 0 2 1 16 0 20
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 0 0 3 11 4 0 18
Athena Diagnostics 0 0 1 3 11 0 15
Variantyx, Inc. 7 8 0 0 0 0 15
Clinical Genetics, Academic Medical Center 1 0 1 4 8 0 14
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 2 3 8 0 0 0 13
Dr. Peter K. Rogan Lab, Western University 0 0 0 0 0 12 12
Centre for Mendelian Genomics, University Medical Centre Ljubljana 3 4 4 0 0 0 11
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 2 0 0 0 9 0 11
Clinical Biomedical Laboratory, Shriners Hospital For Children - Canada 8 2 0 0 0 0 10
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 3 3 4 0 0 0 10
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 6 4 0 0 0 0 10
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 3 5 2 0 0 0 10
Laboratory of Functional Genomics, Research Centre for Medical Genetics 2 4 4 0 0 0 10
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 5 4 1 0 0 0 10
Baylor Genetics 6 1 2 0 0 0 9
MGZ Medical Genetics Center 2 5 2 0 0 0 9
Clinical Genetics Laboratory, Skane University Hospital Lund 2 3 3 0 0 0 8
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi 1 6 1 0 0 0 8
Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg 2 0 6 0 0 0 8
Institute of Human Genetics, University of Leipzig Medical Center 2 2 3 0 1 0 8
Neuberg Centre For Genomic Medicine, NCGM 2 2 4 0 0 0 8
Center of Medical Genetics, Central South University 2 2 1 1 1 0 7
Genetics and Molecular Pathology, SA Pathology 1 3 2 0 0 0 6
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 1 5 0 0 0 0 6
Laboratory of Genetics, Children's Clinical University Hospital Latvia 0 0 0 3 3 0 6
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 3 3 0 0 0 0 6
GeneReviews 0 0 0 0 0 5 5
GenomeConnect, ClinGen 0 0 0 0 0 5 5
Institute of Human Genetics Munich, TUM University Hospital 5 0 0 0 0 0 5
MVZ Martinsried, Medicover Genetics 0 3 2 0 0 0 5
MVZ Medizinische Genetik Mainz 1 3 1 0 0 0 5
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 1 2 1 0 0 0 4
Centre of Medical Genetics, University Hospital Muenster 1 3 0 0 0 0 4
Dasa 4 0 0 0 0 0 4
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 3 1 0 0 0 0 4
Institute Of Reproduction And Development, Obstetrics and Gynecology Hospital, Fudan University 1 3 0 0 0 0 4
Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital 0 4 0 0 0 0 4
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 2 0 0 1 0 0 3
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 1 1 0 0 0 3
DBGen Ocular Genomics 2 0 1 0 0 0 3
Department of Otolaryngology – Head & Neck Surgery, Cochlear Implant Center 0 1 1 0 1 0 3
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 3 0 0 0 3
Division of Human Genetics, National Health Laboratory Service/University of the Witwatersrand 2 1 0 0 0 0 3
Genetics Laboratory, Great Ormond Street Hospital NHS Foundation Trust, North Thames Genomic Laboratory Hub 0 1 2 0 0 0 3
Institute of Human Genetics, Cologne University 1 2 0 0 0 0 3
Institute of Human Genetics, University Medical Center Hamburg-Eppendorf 0 2 1 0 0 0 3
Johns Hopkins Genomics, Johns Hopkins University 2 1 0 0 0 0 3
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 2 1 0 0 0 3
MVZ Praenatalmedizin und Genetik Nuernberg 1 0 0 2 0 0 3
Medical and Scientific Branch, Hong Kong Genome Institute 1 2 0 0 0 0 3
Molecular Genetics, Royal Melbourne Hospital 1 1 1 0 0 0 3
Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital 0 2 0 0 0 0 2
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 1 1 0 0 0 0 2
CENTOGENE GmbH and LLC - Guiding Precision Medicine 0 1 1 0 0 0 2
Center for Medical Genetics Ghent, University of Ghent 2 0 0 0 0 0 2
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 0 0 0 2 0 0 2
Department of Human Genetics, Hannover Medical School 0 2 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 Molecular Genetics, Istishari Arab Hospital 0 2 0 0 0 0 2
Division of Genetic & Genomic Pathology, Hong Kong Children's Hospital 1 1 0 0 0 0 2
Division of Genomic Medicine, Department of Advanced Medicine, Medical Research Institute, Kanazawa Medical University 2 0 0 0 0 0 2
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia 0 0 1 1 0 0 2
Genomic Medicine Lab, University of California San Francisco 1 1 0 0 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 1 0 0 0 2
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden 1 0 1 0 0 0 2
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 2 0 0 0 0 0 2
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 0 1 0 0 0 2
Institute of Human Genetics, University of Goettingen 0 1 1 0 0 0 2
Laboratório de Genética Molecula, r University of Campinas - Unicamp 0 0 0 0 0 2 2
Miami Human Genetics, University Of Miami Miller School Of Medicine 1 0 1 0 0 0 2
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 2 0 0 0 0 0 2
Sharon lab, Hadassah-Hebrew University Medical Center 2 0 0 0 0 0 2
Suma Genomics 1 1 0 0 0 0 2
Undiagnosed Diseases Network, NIH 1 1 0 0 0 0 2
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine 1 0 0 0 0 0 1
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital 1 0 0 0 0 0 1
Center for Human Genetics and Genomic Medicine, Uniklinik Rwth Aachen 0 1 0 0 0 0 1
Center for Personalized Medicine, Children's Hospital Los Angeles 1 0 0 0 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 0 0 0 0 1
Centre of Medical Genetics, University of Antwerp 1 0 0 0 0 0 1
Clinical Genomics Laboratory, Washington University in St. Louis 1 0 0 0 0 0 1
Department of Clinical Genetics, Aarhus University Hospital 1 0 0 0 0 0 1
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet 0 0 1 0 0 0 1
Department of Clinical Pathology, School of Medicine, Fujita Health University 0 0 0 1 0 0 1
Department of Endocrinology, Genetics and Metabolism, Shanghai Children's Medical Center 0 0 1 0 0 0 1
Department of Genetics, Beijing BioBiggen Technology Co., Ltd. 1 0 0 0 0 0 1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine 0 1 0 0 0 0 1
Department of Genetics, Sultan Qaboos University Hospital 0 1 0 0 0 0 1
Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine 1 0 0 0 0 0 1
Department of Paediatrics at Addenbrookes, Cambridge University Hospitals NHS Foundation Trust (UK) 0 0 1 0 0 0 1
Department of Pediatrics, Inha University Hospital, Inha University College of Medicine 0 1 0 0 0 0 1
Department of Pediatrics, The First Affiliated Hospital of Wenzhou Medical University 1 0 0 0 0 0 1
Dept. Genetics and Cancer, Menzies Institute for Medical Research, University of Tasmania 1 0 0 0 0 0 1
Eurofins-Biomnis 1 0 0 0 0 0 1
Faculty of Pharmacy, University of Ljubljana 0 0 1 0 0 0 1
Genetic Laboratory, Lianyungang Maternal and Child Health Hospital Affiliated to Kangda College of Nanjing Medical University 0 1 0 0 0 0 1
GenomeConnect - Brain Gene Registry 0 0 0 0 0 1 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1
Grupo de Genetica Humana, Facultad de Medicina - Universidad de La Sabana 0 0 1 0 0 0 1
Hacettepe Pediatric Genetics Laboratory, Hacettepe University 1 0 0 0 0 0 1
Hadassah Hebrew University Medical Center 0 1 0 0 0 0 1
Hunan Provincial Maternal and Child Health Care Hospital 0 1 0 0 0 0 1
Imagene.me medical diagnostic laboratory, IMAGENE.ME SA 1 0 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, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg 1 0 0 0 0 0 1
Institute of Human Genetics, University Hospital of Duesseldorf 0 1 0 0 0 0 1
Institute of Immunology and Genetics Kaiserslautern 0 1 0 0 0 0 1
Institute of Medical Genetics, Medical University of Vienna 1 0 0 0 0 0 1
Intergen Genetics and Rare Diseases Diagnosis Center 0 1 0 0 0 0 1
Kariminejad - Najmabadi Pathology & Genetics Center 0 1 0 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 1 0 0 0 0 1
Laboratory of Prof. Karen Avraham, Tel Aviv University 0 0 1 0 0 0 1
Medical Genetics UMG, Mater Domini University Hospital/ Magna Graecia University of Catanzaro 1 0 0 0 0 0 1
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute 0 0 1 0 0 0 1
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals 0 1 0 0 0 0 1
Molecular Oncology Research Center, Barretos Cancer Hospital 0 0 1 0 0 0 1
NHS Central & South Genomic Laboratory Hub 1 0 0 0 0 0 1
New York Genome Center 0 0 1 0 0 0 1
Ocular Genomics Institute, Massachusetts Eye and Ear 0 1 0 0 0 0 1
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations 0 0 1 0 0 0 1
Programa de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília 1 0 0 0 0 0 1
Rheumatology and Immunology Department, Shandong Provincial Hospital Affiliated to Shandong First Medicial University 1 0 0 0 0 0 1
Synevo Romania 0 1 0 0 0 0 1
WangQJ Lab, Chinese People's Liberation Army General Hospital 0 1 0 0 0 0 1
Zankl Lab, University of Sydney 1 0 0 0 0 0 1

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