ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*670G>T

gnomAD frequency: 0.00016  dbSNP: rs182613927
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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 RCV000357584 SCV000367578 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494948 SCV002785350 uncertain significance Long QT syndrome 10 2021-08-18 criteria provided, single submitter clinical testing

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