ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.-139dup

dbSNP: rs879019805
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000407602 SCV000471959 uncertain significance Benign neonatal seizures 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000310875 SCV000471960 uncertain significance Benign Neonatal Epilepsy 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001653732 SCV001869424 benign not provided 2019-08-18 criteria provided, single submitter clinical testing

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