ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.8613G>A (p.Leu2871=)

dbSNP: rs780211536
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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 RCV001438975 SCV001641856 likely benign Long QT syndrome 2020-07-22 criteria provided, single submitter clinical testing

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