ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2706C>T (p.Thr902=)

gnomAD frequency: 0.00001  dbSNP: rs752943013
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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 RCV001426296 SCV001628946 likely benign Glycine encephalopathy 2023-07-11 criteria provided, single submitter clinical testing

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