ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.2316-18C>T

dbSNP: rs1330113346
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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 RCV002188354 SCV002487464 likely benign Glycine encephalopathy 2024-05-17 criteria provided, single submitter clinical testing

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