ClinVar Miner

Submissions for variant NM_181798.1(KCNQ1):c.637_639del (p.Phe213del) (rs397508069)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000003277 SCV000023435 pathogenic Long QT syndrome 1 1998-08-01 no assertion criteria provided literature only
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577653 SCV000678860 not provided Long QT syndrome, LQT1 subtype no assertion provided literature only

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