ClinVar Miner

Submissions for variant NC_012920.1:m.7445A>T

dbSNP: rs199474818
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000778058 SCV002517658 pathogenic Mitochondrial non-syndromic sensorineural hearing loss 2022-05-04 criteria provided, single submitter clinical testing
GeneReviews RCV000778058 SCV000914174 not provided Mitochondrial non-syndromic sensorineural hearing loss no assertion provided literature only

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