ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.8161-6T>A

gnomAD frequency: 0.00001  dbSNP: rs554984079
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000369912 SCV000470301 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001465275 SCV001669258 likely benign Long QT syndrome 2023-03-14 criteria provided, single submitter clinical testing

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