ClinVar Miner

Submissions for variant NM_174934.3(SCN4B):c.-178C>T

dbSNP: rs865930367
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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 RCV000334863 SCV000367612 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004692985 SCV005192079 uncertain significance not provided criteria provided, single submitter not provided

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