ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.-148_-147insTG

dbSNP: rs886062698
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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 RCV000285110 SCV000471971 uncertain significance Benign Neonatal Epilepsy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000324055 SCV000471972 uncertain significance Benign neonatal seizures 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002292442 SCV002586244 benign not provided 2023-03-01 criteria provided, single submitter clinical testing KCNQ3: BS1, BS2

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