ClinVar Miner

Submissions for variant NM_004453.4(ETFDH):c.1469-8T>C

dbSNP: rs1774625470
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001279060 SCV001699671 likely benign Multiple acyl-CoA dehydrogenase deficiency 2023-04-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279060 SCV001466120 uncertain significance Multiple acyl-CoA dehydrogenase deficiency 2020-04-21 no assertion criteria provided clinical testing

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