ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.938-11_938-10delinsTA

dbSNP: rs2136003778
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002182877 SCV002344978 likely benign Long QT syndrome 2023-10-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494064 SCV002798472 likely benign Long QT syndrome 13; Familial hyperaldosteronism type III 2021-08-29 criteria provided, single submitter clinical testing

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