ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*2196G>A

gnomAD frequency: 0.00031  dbSNP: rs769472607
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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 RCV000312225 SCV000367508 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002487346 SCV002781527 uncertain significance Long QT syndrome 10 2021-09-28 criteria provided, single submitter clinical testing

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