ClinVar Miner

Submissions for variant NM_021098.2(CACNA1H):c.[2318G>A;2362C>T]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000002823 SCV000022981 risk factor Epilepsy, childhood absence, susceptibility to, 6 2005-05-11 no assertion criteria provided literature only

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