ClinVar Miner

Submissions for variant m.9537dupC (rs267606614)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000144008 SCV000188900 pathogenic Leigh syndrome 2014-04-17 no assertion criteria provided literature only
OMIM RCV000010292 SCV000030516 pathogenic Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency 2000-11-01 no assertion criteria provided literature only

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