ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.*108G>A

gnomAD frequency: 0.00048  dbSNP: rs180795690
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000363618 SCV000447241 uncertain significance Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing

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