ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.3057T>A (p.Ser1019=)

dbSNP: rs2129641056
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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 RCV001409750 SCV001611783 likely benign Glycine encephalopathy 2020-02-18 criteria provided, single submitter clinical testing

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