ClinVar Miner

Submissions for variant NM_174934.4(SCN4B):c.*961A>G

gnomAD frequency: 0.00058  dbSNP: rs561492722
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000326851 SCV000367560 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002480102 SCV002779063 uncertain significance Long QT syndrome 10 2021-09-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004692984 SCV005192057 uncertain significance not provided criteria provided, single submitter not provided

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