ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.6913C>A (p.Pro2305Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002613011 SCV002954543 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2022-02-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005019264 SCV005645218 uncertain significance Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV 2024-05-13 criteria provided, single submitter clinical testing

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