ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2844T>G (p.Ser948=)

dbSNP: rs1817084254
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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 RCV001463830 SCV001667778 likely benign Glycine encephalopathy 2020-09-03 criteria provided, single submitter clinical testing

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