ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2457+17T>A

gnomAD frequency: 0.00009  dbSNP: rs371788223
Minimum review status: Collection method:
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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 RCV002031936 SCV002310187 likely benign Glycine encephalopathy 2024-05-20 criteria provided, single submitter clinical testing

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