ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.500_502del (p.Phe167_Gly168delinsTrp)

dbSNP: rs397508113
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000003259 SCV000023417 pathogenic Long QT syndrome 1 1996-01-01 no assertion criteria provided literature only
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000003259 SCV000678871 not provided Long QT syndrome 1 no assertion provided literature only

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