ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.15C>A (p.Ala5=)

dbSNP: rs1217742509
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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 RCV001504812 SCV001709698 likely benign Glycine encephalopathy 2021-12-21 criteria provided, single submitter clinical testing

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