ClinVar Miner

Submissions for variant NM_004519.4(KCNQ3):c.-136_-134dup

dbSNP: rs886062695
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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 RCV000377033 SCV000471953 uncertain significance Benign Neonatal Epilepsy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000284935 SCV000471954 uncertain significance Benign neonatal seizures 2016-06-14 criteria provided, single submitter clinical testing

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