ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1591-19G>A

gnomAD frequency: 0.00003  dbSNP: rs1167627067
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001609780 SCV001839757 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072913 SCV002487661 likely benign Long QT syndrome 2024-09-06 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004699438 SCV005203700 likely benign not specified 2024-07-03 criteria provided, single submitter clinical testing

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