ClinVar Miner

Submissions for variant NM_003098.2(SNTA1):c.-251G>A

gnomAD frequency: 0.00001  dbSNP: rs886056630
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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 RCV000327401 SCV000433532 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000384339 SCV000433533 uncertain significance Congenital long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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