ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.1189G>A (p.Gly397Arg)

dbSNP: rs2125638599
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV002277656 SCV002564467 uncertain significance Neurodevelopmental disorder 2021-12-17 criteria provided, single submitter clinical testing

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