ClinVar Miner

Variants in gene DNAH9

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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
97 74 1103 888 245 27 2323

Condition and significance breakdown #

Total conditions: 34
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
not provided 87 39 634 831 241 0 1809
Inborn genetic diseases 0 0 598 32 0 0 630
DNAH9-related disorder 2 12 37 67 49 0 167
Ciliary dyskinesia, primary, 40 13 31 61 9 11 0 121
not specified 0 0 0 2 37 0 39
Primary ciliary dyskinesia 0 1 8 0 0 0 9
Gastric cancer 0 0 0 0 0 6 6
Lung cancer 0 0 0 0 0 4 4
Uterine corpus endometrial carcinoma 0 0 0 0 0 4 4
Fetal anomalies with a likely genetic cause 3 0 0 0 0 0 3
Sarcoma 0 0 0 0 0 3 3
Thyroid cancer, nonmedullary, 1 0 0 0 0 0 3 3
Abnormal cardiovascular system morphology 0 0 2 0 0 0 2
Cervical cancer 0 0 0 0 0 2 2
Clear cell carcinoma of kidney 0 0 0 0 0 2 2
Congenital heart disease 2 0 0 0 0 0 2
Hydrocephalus 0 2 0 0 0 0 2
Melanoma 0 0 0 0 0 2 2
Ovarian serous cystadenocarcinoma 0 0 0 0 0 2 2
Acute myeloid leukemia 0 0 0 0 0 1 1
Cholangiocarcinoma 0 0 0 0 0 1 1
Ciliary dyskinesia, primary, 50 0 1 0 0 0 0 1
Colon adenocarcinoma 0 0 0 0 0 1 1
Congenital heart disease; Congenital anomaly of kidney and urinary tract 0 0 1 0 0 0 1
Glioma susceptibility 1 0 0 0 0 0 1 1
Male infertility 0 0 1 0 0 0 1
Malignant tumor of esophagus 0 0 0 0 0 1 1
Malignant tumor of urinary bladder 0 0 0 0 0 1 1
Schizophrenia 0 0 1 0 0 0 1
See cases 0 0 0 1 0 0 1
Sinoatrial node dysfunction and deafness 0 0 1 0 0 0 1
Squamous cell carcinoma of the head and neck 0 0 0 0 0 1 1
Squamous cell lung carcinoma 0 0 0 0 0 1 1
Uterine carcinosarcoma 0 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 47
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 87 36 586 814 140 0 1663
Ambry Genetics 0 0 598 32 0 0 630
GeneDx 1 1 54 0 139 0 195
PreventionGenetics, part of Exact Sciences 2 12 37 67 49 0 167
Breakthrough Genomics, Breakthrough Genomics 0 0 14 7 142 0 163
Mayo Clinic Laboratories, Mayo Clinic 0 0 12 9 33 0 54
CeGaT Center for Human Genetics Tuebingen 1 0 20 26 3 0 50
Dr. Peter K. Rogan Lab, Western University 0 0 0 0 0 27 27
Fulgent Genetics, Fulgent Genetics 0 5 7 9 1 0 22
Revvity Omics, Revvity 2 5 12 0 0 0 19
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 0 0 0 15 0 15
3billion 2 3 8 0 0 0 13
Department of Pathology and Laboratory Medicine, Sinai Health System 1 5 5 0 0 0 11
Genome-Nilou Lab 0 0 0 0 10 0 10
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 3 7 0 0 0 10
Johns Hopkins Genomics, Johns Hopkins University 0 2 7 0 0 0 9
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill 0 1 8 0 0 0 9
OMIM 8 0 0 0 0 0 8
Baylor Genetics 0 2 5 0 0 0 7
First Genomix Gene Laboratory, Genetic Diagnostics Department 2 5 0 0 0 0 7
Genetics and Molecular Pathology, SA Pathology 1 1 3 0 0 0 5
Laboratory of Genetics, Children's Clinical University Hospital Latvia 0 1 0 2 2 0 5
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden 0 0 4 0 0 0 4
Genetics Laboratory, Great Ormond Street Hospital NHS Foundation Trust, North Thames Genomic Laboratory Hub 3 0 0 0 0 0 3
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 2 0 0 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 2 0 0 0 2
Institute of Human Genetics, University of Wuerzburg 0 2 0 0 0 0 2
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 2 0 0 0 0 2
Istanbul Faculty of Medicine, Istanbul University 2 0 0 0 0 0 2
Juno Genomics, Hangzhou Juno Genomics, Inc 2 0 0 0 0 0 2
Neuberg Centre For Genomic Medicine, NCGM 0 0 2 0 0 0 2
New York Genome Center 0 0 2 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 2 0 0 0 2
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 1 0 0 0 0 0 1
Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University 0 0 1 0 0 0 1
Center of Excellence for Medical Genomics, Chulalongkorn University 1 0 0 0 0 0 1
Department of Psychiatry, The University of Hong Kong 0 0 1 0 0 0 1
Division of Clinical Immunology and Allergy, Necmettin Erbakan University, Faculty of Medicine 0 0 1 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 1 0 0 0 0 0 1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 0 0 0 0 0 1
ISCA Site 6 0 0 0 1 0 0 1
Institute Of Molecular Biology And Genetics, Federal Almazov National Medical Research Centre 0 0 1 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 0 1
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology 0 1 0 0 0 0 1
Optical Genome Mapping Laboratory, Clinical Institute of Genomic Medicine, University Medical Center Ljubljana 0 0 1 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 1 0 0 0 0 1
Variantyx, Inc. 0 1 0 0 0 0 1

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