ClinVar Miner

Submissions for variant NC_012920.1(MT-TS1):m.7445A>C

dbSNP: rs199474818
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000010181 SCV002517656 pathogenic Mitochondrial non-syndromic sensorineural hearing loss 2022-05-04 criteria provided, single submitter clinical testing
OMIM RCV000010181 SCV000030404 pathogenic Mitochondrial non-syndromic sensorineural hearing loss 2007-09-14 no assertion criteria provided literature only
GeneReviews RCV000010181 SCV000172236 not provided Mitochondrial non-syndromic sensorineural hearing loss no assertion provided literature only

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