ClinVar Miner

Submissions for variant NM_003850.3(SUCLA2):c.90+24G>A

gnomAD frequency: 0.71769  dbSNP: rs9567972
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001815648 SCV002062216 benign Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707735 SCV005230261 benign not provided criteria provided, single submitter not provided

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