ClinVar Miner

Submissions for variant NM_001985.3(ETFB):c.216+18del

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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 RCV003039409 SCV003335756 benign Multiple acyl-CoA dehydrogenase deficiency 2023-02-18 criteria provided, single submitter clinical testing

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