ClinVar Miner

Submissions for variant NM_001161352.2(KCNMA1):c.-101_-96dup

dbSNP: rs545094311
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000271650 SCV000365146 likely benign Generalized epilepsy-paroxysmal dyskinesia syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001618521 SCV001847379 benign not provided 2018-07-15 criteria provided, single submitter clinical testing

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