ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.1041C>G (p.Pro347=)

dbSNP: rs545444296
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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 RCV001415855 SCV001618024 likely benign Long QT syndrome 2019-09-23 criteria provided, single submitter clinical testing

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