ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.8161-7G>A

gnomAD frequency: 0.00019  dbSNP: rs202218770
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001397425 SCV001599172 likely benign Long QT syndrome 2023-12-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002493947 SCV002800322 likely benign Long QT syndrome 11 2021-07-28 criteria provided, single submitter clinical testing

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