ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.3304G>A (p.Asp1102Asn)

dbSNP: rs1555514961
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV000660379 SCV000782454 uncertain significance Epilepsy, childhood absence, susceptibility to, 6 2016-06-23 criteria provided, single submitter clinical testing

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