ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.11330+7A>G

gnomAD frequency: 0.00004  dbSNP: rs781216766
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000865994 SCV001857161 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002064526 SCV002402361 benign Long QT syndrome 2021-08-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002253629 SCV002524895 benign Long QT syndrome 11 2021-12-05 criteria provided, single submitter clinical testing

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