Variants studied for Amyotrophic lateral sclerosis type 6

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
16	8	89	18	37	166

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	total
FUS	15	8	89	18	37	165
VCP	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	1	0	83	18	35	137
OMIM	10	0	0	0	0	10
Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University	2	3	0	0	0	5
Mendelics	0	1	1	0	2	4
Neuberg Centre For Genomic Medicine, NCGM	2	0	1	0	0	3
Athena Diagnostics	0	0	0	0	2	2
Neurogenomics Lab, Neuroscience Institute, University Of Cape Town	0	1	1	0	0	2
Baylor Genetics	0	1	0	0	0	1
Institute of Human Genetics, Cologne University	1	0	0	0	0	1
MGZ Medical Genetics Center	0	0	1	0	0	1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	1	0	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	1	0	0	1
Neurology Department，The First Affiliated Hospital of Zhengzhou University, Zhengzhou University	1	0	0	0	0	1
3billion	0	1	0	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	1	0	0	1
Department of Research, Sir Ganga Ram Hospital	0	1	0	0	0	1

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