ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.2529T>C (p.Asp843=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005182997 SCV005809519 likely benign Brugada syndrome 2024-10-01 criteria provided, single submitter clinical testing

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