ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*989dup

dbSNP: rs5795117
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000285012 SCV000367548 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000342323 SCV000367549 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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