ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5862C>G (p.Thr1954=)

dbSNP: rs945227847
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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 RCV001469969 SCV001674059 likely benign Long QT syndrome 2020-06-01 criteria provided, single submitter clinical testing

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