ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1935C>G (p.Leu645=)

dbSNP: rs1192928029
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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 RCV001442786 SCV001645741 likely benign Glycine encephalopathy 2023-04-14 criteria provided, single submitter clinical testing

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