ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.7087T>C (p.Leu2363=)

dbSNP: rs2130860874
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001395473 SCV001597186 likely benign Long QT syndrome 2019-04-27 criteria provided, single submitter clinical testing

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