ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.477+3521G>A

gnomAD frequency: 0.17068  dbSNP: rs11823023
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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 RCV001511442 SCV001718685 benign Long QT syndrome 2025-01-15 criteria provided, single submitter clinical testing

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