ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1394-3158C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003326816 SCV004033103 benign not provided 2025-02-01 criteria provided, single submitter clinical testing KCNQ1OT1: BS1, BS2

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