ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.8595A>C (p.Ile2865=)

gnomAD frequency: 0.00002  dbSNP: rs760511790
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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 RCV000863101 SCV001003702 benign Long QT syndrome 2021-05-26 criteria provided, single submitter clinical testing

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