ClinVar Miner

Submissions for variant NM_004453.4(ETFDH):c.832-3dup

dbSNP: rs376153836
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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 RCV002129825 SCV002404229 benign Multiple acyl-CoA dehydrogenase deficiency 2025-01-29 criteria provided, single submitter clinical testing

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