Variants studied for Arthrogryposis, distal, type 2B2

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
3	3	6	0	6	15

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
TNNT3	3	3	6	6	15

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	0	6	6
OMIM	2	0	0	0	2
Baylor Genetics	1	0	1	0	2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	1	1	0	2
SIB Swiss Institute of Bioinformatics	1	1	0	0	2
MGZ Medical Genetics Center	1	0	0	0	1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	1	0	0	1
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine	0	0	1	0	1
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust	1	0	0	0	1
Institute of Human Genetics, University Hospital of Duesseldorf	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	1
New York Genome Center	1	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	1
Genetic Diagnostics Department, Viafet Genomics Laboratory	0	0	1	0	1

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