ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2859C>G (p.Thr953=)

dbSNP: rs1817083513
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001209030 SCV001380449 likely benign Glycine encephalopathy 2024-12-31 criteria provided, single submitter clinical testing
Natera, Inc. RCV001209030 SCV002075709 uncertain significance Glycine encephalopathy 2020-11-16 no assertion criteria provided clinical testing

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