ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.642C>T (p.Asn214=)

gnomAD frequency: 0.00011  dbSNP: rs775546889
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 RCV000548690 SCV000636413 likely benign Glycine encephalopathy 2025-01-06 criteria provided, single submitter clinical testing

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