Variants studied for intellectual developmental disorder with severe speech and ambulation defects

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
5	7	6	0	1	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
ACTL6B	5	7	6	1	15

Submitter and significance breakdown #

Total submitters: 18

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Baylor Genetics	3	1	0	0	4
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	2	0	3
OMIM	2	0	0	0	2
SIB Swiss Institute of Bioinformatics	0	1	1	0	2
Solve-RD Consortium	0	2	0	0	2
MGZ Medical Genetics Center	0	1	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	1	0	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	0	1	0	0	1
Genome-Nilou Lab	0	0	0	1	1
3billion	0	1	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein	0	0	1	0	1
Houlden Lab, UCL Institute of Neurology	1	0	0	0	1
Laboratory of genome editing, Research Centre for Medical Genetics	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	1	0	0	1

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