ClinVar Miner

Variants studied for catecholaminergic polymorphic ventricular tachycardia 3

Included ClinVar conditions (1):
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
3 5 4 0 0 11

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
TECRL 3 5 4 11

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance total
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 2 2 4
OMIM 3 0 0 3
Baylor Genetics 0 1 1 2
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 1 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 1
Molecular and Cytogenetics Laboratory, Americain University of Beirut Medical Center 0 1 0 1

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