Variants studied for Slowed nerve conduction velocity, autosomal dominant

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
1	0	12	4	13	29

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	uncertain significance	likely benign	benign	total
ARHGEF10	1	12	4	13	29

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	uncertain significance	likely benign	benign	total
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories	0	2	1	7	10
Genome Diagnostics Laboratory,University Medical Center Utrecht	0	0	3	2	5
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen	0	0	0	5	5
Baylor Genetics	0	4	0	0	4
Institute of Human Genetics,Cologne University	0	2	0	0	2
Centre for Mendelian Genomics,University Medical Centre Ljubljana	0	2	0	0	2
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center	0	0	1	1	2
OMIM	1	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	0	1
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues	0	1	0	0	1

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