ClinVar Miner

Variants studied for Aminoglycoside-induced deafness

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 drug response total
13 66 0 0 0 2 79

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic drug response total
TRMU 7 66 0 73
MT-RNR1 3 0 0 3
MT-CO1, MT-TS1 1 0 0 1
MT-ND1, MT-RNR1 1 0 1 1
MT-RNR1, MT-TS1 1 0 1 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic likely pathogenic drug response total
Baylor Genetics 7 66 0 73
OMIM 6 0 0 6
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 2 2

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