ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.4918-10dup

dbSNP: rs755283199
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674631 SCV001889586 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502016 SCV002807222 likely benign Long QT syndrome 11 2021-09-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002538593 SCV003519076 benign Long QT syndrome 2024-01-15 criteria provided, single submitter clinical testing

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