ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.1212+12C>T

dbSNP: rs8060577
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001641793 SCV001860662 benign not provided 2019-07-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072996 SCV002405331 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2024-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001641793 SCV005296405 benign not provided criteria provided, single submitter not provided

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