ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5706A>G (p.Glu1902=)

dbSNP: rs537002656
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000178565 SCV000230670 uncertain significance not provided 2015-04-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001082015 SCV000627573 benign Long QT syndrome 2023-10-14 criteria provided, single submitter clinical testing

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