ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1161C>G (p.Leu387=)

dbSNP: rs781613958
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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 RCV002152153 SCV002415416 likely benign Glycine encephalopathy 2022-08-23 criteria provided, single submitter clinical testing

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