ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.3153-13C>T

gnomAD frequency: 0.00006  dbSNP: rs372337645
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000310070 SCV000467506 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001841272 SCV001349846 likely benign Cardiac arrhythmia 2019-01-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000310070 SCV002382825 likely benign Long QT syndrome 2024-12-30 criteria provided, single submitter clinical testing

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