ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.3224+17del

dbSNP: rs1563823565
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002132420 SCV002402752 benign Long QT syndrome 2021-11-12 criteria provided, single submitter clinical testing

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