ClinVar Miner

Submissions for variant NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCCGTC

dbSNP: rs1555854855
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001711478 SCV001940556 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
GeneDx RCV000187829 SCV000241427 benign not specified 2013-10-23 flagged submission clinical testing The variant is found in INFANT-EPI,EPILEPSY panel(s).

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