ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1743C>T (p.Pro581=)

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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 RCV003625112 SCV004403488 likely benign Glycine encephalopathy 2024-01-24 criteria provided, single submitter clinical testing

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