ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.357T>C (p.Thr119=)

gnomAD frequency: 0.00001  dbSNP: rs777954190
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001436339 SCV001639181 likely benign Glycine encephalopathy 2024-02-26 criteria provided, single submitter clinical testing

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