ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.9124C>T (p.Leu3042=)

dbSNP: rs1447756030
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001401840 SCV001603674 likely benign Long QT syndrome 2021-06-09 criteria provided, single submitter clinical testing
GeneDx RCV000867539 SCV001866176 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002253632 SCV002524872 benign Long QT syndrome 11 2021-12-05 criteria provided, single submitter clinical testing

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