ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.880C>T (p.Leu294=)

dbSNP: rs2135999678
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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 RCV002188320 SCV002483585 likely benign Long QT syndrome 2020-12-19 criteria provided, single submitter clinical testing

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