ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.2965+12G>A

gnomAD frequency: 0.00001  dbSNP: rs755987120
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001619461 SCV001847609 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002072942 SCV002486771 likely benign Long QT syndrome 2023-10-16 criteria provided, single submitter clinical testing

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