ClinVar Miner

Submissions for variant NM_000170.3(GLDC):c.27del (p.Leu10fs)

dbSNP: rs1414541286
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528609 SCV001740597 pathogenic not provided no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001528609 SCV001800646 likely pathogenic not provided no assertion criteria provided clinical testing

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