ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.11687-16T>C

gnomAD frequency: 0.00005  dbSNP: rs549524911
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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 RCV002154982 SCV002334484 likely benign Long QT syndrome 2024-01-23 criteria provided, single submitter clinical testing

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