ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1083_1088dup (p.Lys362_His363insGlnLys)

dbSNP: rs397508076
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577377 SCV000678862 not provided Long QT syndrome 1 no assertion provided literature only

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