ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2289T>C (p.Gly763=)

gnomAD frequency: 0.00002  dbSNP: rs749032015
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 RCV002088268 SCV002378673 likely benign Glycine encephalopathy 2021-09-27 criteria provided, single submitter clinical testing

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