ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1974C>T (p.Ala658=)

dbSNP: rs534062853
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001399430 SCV001601220 likely benign Glycine encephalopathy 2024-04-25 criteria provided, single submitter clinical testing

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