ClinVar Miner

Submissions for variant NM_033337.3(CAV3):c.446AGG[1] (p.Glu150del)

dbSNP: rs1027684031
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV001089530 SCV001244884 uncertain significance Long QT syndrome 9 2019-09-17 criteria provided, single submitter clinical testing

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