ClinVar Miner

Submissions for variant NM_001379210.1(SLC25A26):c.*3C>A

gnomAD frequency: 0.02088  dbSNP: rs116677829
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707402 SCV001936426 benign not provided 2020-06-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807513 SCV002055909 benign Combined oxidative phosphorylation deficiency 28 2021-07-15 criteria provided, single submitter clinical testing

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