ClinVar Miner

Variants studied for Diabetes-deafness syndrome maternally transmitted

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
4 1 0 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic total
MT-TE 2 0 2
MT-TK 1 0 1
MT-TL1 1 0 1
MT-TL2 0 1 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic total
OMIM 4 0 4
Institute of Human Genetics, University of Leipzig Medical Center 1 0 1
Unidad de Genómica Médica UC, Pontificia Universidad Católica de Chile 1 0 1
Department of Clinical Genetics, Medical University of Lodz 0 1 1

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