ClinVar Miner

Submissions for variant NM_005327.7(HADH):c.827-9G>A

gnomAD frequency: 0.00002  dbSNP: rs1363052334
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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 RCV002110848 SCV002433090 likely benign Deficiency of 3-hydroxyacyl-CoA dehydrogenase 2023-12-01 criteria provided, single submitter clinical testing

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