ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.3796+18G>A

gnomAD frequency: 0.02360  dbSNP: rs66792339
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001841515 SCV000051981 uncertain Cardiac arrhythmia 2011-08-18 criteria provided, single submitter curation Converted during submission to Uncertain significance.
GeneDx RCV001650843 SCV001869513 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002054478 SCV002355258 benign Long QT syndrome 2024-01-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001650843 SCV004564119 benign not provided 2023-11-29 criteria provided, single submitter clinical testing

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