ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.8020-12G>A

gnomAD frequency: 0.00001  dbSNP: rs779767584
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654123 SCV001863812 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002538526 SCV003471482 likely benign Long QT syndrome 2023-02-09 criteria provided, single submitter clinical testing

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