ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.1644A>G (p.Arg548=)

dbSNP: rs886062468
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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 RCV000399538 SCV000470210 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058675 SCV002445596 likely benign Long QT syndrome 2021-02-14 criteria provided, single submitter clinical testing

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