ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.2544C>T (p.Gly848=)

dbSNP: rs28365123
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000546311 SCV000632106 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2024-01-30 criteria provided, single submitter clinical testing
GeneDx RCV001712493 SCV001943508 benign not provided 2020-01-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001712493 SCV005296428 benign not provided criteria provided, single submitter not provided

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