Variants studied for arrhythmogenic right ventricular dysplasia 12

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	not provided	total
27	7	623	435	36	3	1081

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
JUP	27	7	620	435	35	3	1077
JUP, LOC130060847	0	0	3	0	1	0	4

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	26	6	552	418	31	0	1033
Illumina Laboratory Services, Illumina	0	0	81	15	10	0	106
Fulgent Genetics, Fulgent Genetics	0	0	90	12	0	0	102
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	5	0	0	0	5
Genome-Nilou Lab	0	0	0	0	5	0	5
GeneReviews	0	0	0	0	0	3	3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	3	0	0	0	3
MGZ Medical Genetics Center	0	0	2	0	0	0	2
New York Genome Center	0	0	2	0	0	0	2
OMIM	1	0	0	0	0	0	1
Baylor Genetics	0	0	1	0	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	0	0	0	1
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine	0	0	1	0	0	0	1
Phosphorus, Inc.	0	0	0	1	0	0	1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein	0	0	1	0	0	0	1
Cardiology, Hunan Children’s Hospital	0	1	0	0	0	0	1

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