Variants studied for Dentinogenesis imperfecta type 2

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
11	5	4	0	4	23

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
DSPP	11	5	4	4	23

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
OMIM	6	0	0	0	6
Genome-Nilou Lab	0	0	0	3	3
Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University	2	0	0	0	2
3billion, Medical Genetics	0	1	1	0	2
Department of Cariology and Endodontology, Peking University School and Hospital of Stomatology	0	2	0	0	2
MGZ Medical Genetics Center	1	0	0	0	1
Mendelics	0	0	0	1	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	1	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	0	0	1	0	1
Center of Genomic medicine, Geneva, University Hospital of Geneva	0	1	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	1	0	0	0	1
Department of Stomatology, Sichuan Provincial People’s Hospital	1	0	0	0	1
Genetic Diagnostics Department, Viafet Genomics Laboratory	0	1	0	0	1

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