Variants studied for Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, 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	not provided	total
5	6	4	0	6	3	23

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	not provided	total
EDAR, RANBP2	5	6	3	6	0	19
EDARADD	0	0	0	0	3	3
EDAR	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	not provided	total
Genome-Nilou Lab	0	0	0	6	0	6
GeneReviews	0	0	0	0	3	3
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	2	0	0	0	0	2
Illumina Laboratory Services, Illumina	0	0	2	0	0	2
Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University	0	2	0	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	1	0	1	0	0	2
Hehr Laboratory, Center for Human Genetics Regensburg	0	1	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	1	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	0	0	1
Division of Human Genetics, Children's Hospital of Philadelphia	1	0	0	0	0	1
Daryl Scott Lab, Baylor College of Medicine	0	0	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	1	0	0	0	0	1
SIB Swiss Institute of Bioinformatics	1	0	0	0	0	1
Biotechnology Lab, Dept of Biomolecular Sciences, University of Urbino	0	1	0	0	0	1
3billion, Medical Genetics	1	0	0	0	0	1

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