ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.4693-10A>T

gnomAD frequency: 0.00678  dbSNP: rs772968330
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000528772 SCV000627734 likely benign Long QT syndrome 2017-05-15 criteria provided, single submitter clinical testing
GeneDx RCV001548056 SCV001767906 likely benign not provided 2018-09-04 criteria provided, single submitter clinical testing

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