ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.3751+16C>G

gnomAD frequency: 0.00003  dbSNP: rs769984472
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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 RCV002097734 SCV002386654 likely benign Long QT syndrome 2023-12-17 criteria provided, single submitter clinical testing

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