ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.896T>A (p.Leu299Ter)

dbSNP: rs1818695432
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV001264015 SCV001442114 likely pathogenic Glycine encephalopathy 2020-02-24 criteria provided, single submitter clinical testing

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