ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.4929+8C>T

dbSNP: rs59027578
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001083004 SCV000632183 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2024-01-26 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000711106 SCV000841433 benign not provided 2018-03-05 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002490984 SCV002795951 likely benign Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV 2021-07-22 criteria provided, single submitter clinical testing

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