ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.1482+19T>C

gnomAD frequency: 0.02433  dbSNP: rs79114789
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516284 SCV001724546 benign Glycine encephalopathy 2025-02-04 criteria provided, single submitter clinical testing
GeneDx RCV001724327 SCV001949603 benign not provided 2018-08-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001724327 SCV005273721 benign not provided criteria provided, single submitter not provided

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