ClinVar Miner

Submissions for variant NM_003849.4(SUCLG1):c.665T>C (p.Leu222Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics RCV003110164 SCV003762165 uncertain significance Mitochondrial DNA depletion syndrome 9 2023-01-31 criteria provided, single submitter clinical testing

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