ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2053-11T>G

gnomAD frequency: 0.00002  dbSNP: rs752086205
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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 RCV002089222 SCV002431146 likely benign Glycine encephalopathy 2024-08-03 criteria provided, single submitter clinical testing

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