ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.6780+1G>A

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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 RCV003389189 SCV004101194 uncertain significance Neurodevelopmental disorder 2023-01-02 criteria provided, single submitter clinical testing

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