ClinVar Miner

Submissions for variant NM_003850.3(SUCLA2):c.27G>A (p.Arg9=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003518675 SCV004354055 likely benign Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria 2023-06-28 criteria provided, single submitter clinical testing

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