ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2181G>T (p.Met727Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234837 SCV003932802 uncertain significance Brugada syndrome 3; Long qt syndrome 8 2023-01-01 criteria provided, single submitter clinical testing

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