ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.10023A>G (p.Glu3341=)

dbSNP: rs2154030257
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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 RCV001485347 SCV001689781 likely benign Long QT syndrome 2020-10-08 criteria provided, single submitter clinical testing

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