ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*986C>G

dbSNP: rs28675746
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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 RCV000274702 SCV000367556 likely benign Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705206 SCV005212273 likely benign not provided criteria provided, single submitter not provided

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