ClinVar Miner

Variants studied for Dentinogenesis imperfecta type 2

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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 3 0 4 22

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 3 4 22

Submitter and significance breakdown #

Total submitters: 13
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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 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
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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