ClinVar Miner

Submissions for variant NM_001931.5(DLAT):c.280-15C>T

dbSNP: rs782149548
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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 RCV002155480 SCV002414891 likely benign Pyruvate dehydrogenase E2 deficiency 2022-11-08 criteria provided, single submitter clinical testing

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