ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.390C>T (p.Gly130=)

dbSNP: rs1585494394
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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 RCV000983519 SCV001131542 likely benign Long QT syndrome 2022-02-05 criteria provided, single submitter clinical testing

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