Variants studied for neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features

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
2	1	24	3	0	29

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	total
ZSWIM6	2	1	24	3	29

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	total
New York Genome Center	1	0	7	0	8
Fulgent Genetics, Fulgent Genetics	0	0	4	3	7
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	2	0	2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	0	2	0	2
Institute of Human Genetics, University of Leipzig Medical Center	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	0	2	0	2
OMIM	1	0	0	0	1
Institute of Human Genetics, University of Goettingen	0	0	1	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	1	0	1
Molecular Genetics Lab, CHRU Brest	0	0	1	0	1
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn	1	0	0	0	1
Pediatric Genetics Clinic, Sheba Medical Center	1	0	0	0	1
Genomics England Pilot Project, Genomics England	0	1	0	0	1
Division Of Personalized Genomic Medicine, Columbia University Irving Medical Center	0	0	1	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	1

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