ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1032+7G>A

dbSNP: rs760839693
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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 RCV002075996 SCV002429874 likely benign Long QT syndrome 2022-07-27 criteria provided, single submitter clinical testing

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