Variants studied for Arrhythmogenic right ventricular dysplasia 2; Catecholaminergic polymorphic ventricular tachycardia 1; Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
0	0	177	18	0	195

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	uncertain significance	likely benign	total
RYR2	157	18	175
LOC126806068, RYR2	13	0	13
LOC126806067, RYR2	7	0	7

Submitter and significance breakdown #

Total submitters: 3

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Submitter	uncertain significance	likely benign	total
Fulgent Genetics, Fulgent Genetics	173	18	191
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	2	0	2
New York Genome Center	2	0	2

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