ClinVar Miner

Submissions for variant NM_001985.3(ETFB):c.58-196_58-194del

dbSNP: rs768440463
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV000721999 SCV002789420 uncertain significance Multiple acyl-CoA dehydrogenase deficiency 2022-05-03 criteria provided, single submitter clinical testing
SingHealth Duke-NUS Institute of Precision Medicine RCV000721999 SCV000853161 uncertain significance Multiple acyl-CoA dehydrogenase deficiency 2017-06-07 no assertion criteria provided curation

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