ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.1965C>G (p.Leu655=)

dbSNP: rs775843731
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000862281 SCV001002764 likely benign Long QT syndrome 2024-01-09 criteria provided, single submitter clinical testing

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