ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1773T>C (p.Tyr591=)

dbSNP: rs2129831810
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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 RCV002189564 SCV002349331 likely benign Glycine encephalopathy 2021-12-25 criteria provided, single submitter clinical testing

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