ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.4245+13del

dbSNP: rs779223487
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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 RCV001519897 SCV001728857 benign Long QT syndrome 2022-09-16 criteria provided, single submitter clinical testing

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