ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.546-14G>T

dbSNP: rs779875096
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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 RCV002213651 SCV002495074 likely benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2023-07-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005017156 SCV005645562 uncertain significance Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV 2024-03-13 criteria provided, single submitter clinical testing

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