ClinVar Miner

Submissions for variant NM_001205293.3(CACNA1E):c.2759G>A (p.Arg920His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002740268 SCV002999494 likely benign not provided 2024-12-10 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002740268 SCV004123893 uncertain significance not provided 2023-10-01 criteria provided, single submitter clinical testing

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