ClinVar Miner

Submissions for variant NM_004453.4(ETFDH):c.175+3A>G

dbSNP: rs781151266
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719067 SCV000728392 likely benign not provided 2021-05-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000925945 SCV001071500 likely benign Multiple acyl-CoA dehydrogenase deficiency 2024-11-12 criteria provided, single submitter clinical testing

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