ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1794T>A (p.Leu598=)

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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 RCV005203667 SCV005837777 likely benign Glycine encephalopathy 2024-10-20 criteria provided, single submitter clinical testing

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