ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*3632del

dbSNP: rs886047715
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000345163 SCV000367466 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000395266 SCV000367467 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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