ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.8020-12G>T

dbSNP: rs779767584
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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 RCV002178095 SCV002348815 likely benign Long QT syndrome 2021-11-11 criteria provided, single submitter clinical testing

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