ClinVar Miner

Variants in gene CALM3

See also:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

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 total
8 3 46 119 19 185

Condition and significance breakdown #

Total conditions: 8
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Long QT syndrome 1 5 1 30 93 10 139
Cardiovascular phenotype 0 0 14 29 1 44
not provided 1 2 8 19 8 37
not specified 0 0 0 8 10 17
Long QT syndrome 16 3 0 2 0 4 9
CALM3-related disorder 0 0 0 2 0 2
Congenital long QT syndrome 0 0 0 0 1 1
Ventricular tachycardia, catecholaminergic polymorphic 6 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 19
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 5 1 30 94 10 140
Ambry Genetics 0 0 13 29 1 43
GeneDx 1 1 6 21 8 37
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 0 2 7 9
Breakthrough Genomics, Breakthrough Genomics 0 0 0 3 6 9
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 2 3 5
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute 0 0 1 0 3 4
CeGaT Center for Human Genetics Tuebingen 0 0 2 2 0 4
OMIM 3 0 0 0 0 3
Clinical Genetics, Academic Medical Center 0 0 0 0 3 3
PreventionGenetics, part of Exact Sciences 0 0 0 2 0 2
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 0 0 2 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 2 0 0 0 0 2
Fulgent Genetics, Fulgent Genetics 0 0 1 0 1 2
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 0 0 0 1 1 2
Genome-Nilou Lab 0 0 0 0 2 2
Stanford Center for Inherited Cardiovascular Disease, Stanford University 0 1 0 0 0 1
New York Genome Center 0 0 1 0 0 1
Razi Pathobiology & Medical Genetics 0 0 0 0 1 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.