ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.438G>T (p.Thr146=)

dbSNP: rs13289273
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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 RCV002073598 SCV002379952 likely benign Glycine encephalopathy 2024-06-02 criteria provided, single submitter clinical testing

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