ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.471-14T>C

gnomAD frequency: 0.00032  dbSNP: rs374248745
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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 RCV002139364 SCV002412666 likely benign Glycine encephalopathy 2025-01-19 criteria provided, single submitter clinical testing

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