ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.6282T>G (p.Leu2094=)

dbSNP: rs2130832903
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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 RCV001476107 SCV001680311 likely benign Long QT syndrome 2019-03-19 criteria provided, single submitter clinical testing

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