ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.589C>T (p.Leu197=)

dbSNP: rs1461615694
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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 RCV001396940 SCV001598678 likely benign Glycine encephalopathy 2022-02-09 criteria provided, single submitter clinical testing

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