Variants studied for Liang-Wang 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	not provided	total
4	5	19	3	1	1	32

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
KCNMA1	4	5	19	3	1	1	32

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	0	0	4	2	0	0	6
New York Genome Center	0	0	5	0	0	0	5
OMIM	4	0	0	0	0	0	4
Institute of Human Genetics, University of Leipzig Medical Center	0	2	1	0	0	0	3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	0	0	2	1	0	0	3
3billion	0	2	1	0	0	0	3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	0	1	0	0	0	1
Centre of Medical Genetics, University of Antwerp	0	1	0	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	0	1	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	0	0	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	0	1	0	0	0	0	1
Breda Genetics srl	0	0	1	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	0	1
GenomeConnect - Brain Gene Registry	0	0	0	0	0	1	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	0	1

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