ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.1946-19C>T

gnomAD frequency: 0.00009  dbSNP: rs369192064
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001716732 SCV001942806 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073339 SCV002406058 benign Long QT syndrome 2025-02-03 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004699445 SCV005204977 benign not specified 2024-06-09 criteria provided, single submitter clinical testing

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