ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.*377del

dbSNP: rs762386874
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000354113 SCV000370469 likely benign Long QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000261614 SCV000370470 likely benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000319600 SCV000370471 likely benign Short QT syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000367323 SCV000370472 likely benign Jervell and Lange-Nielsen syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001731581 SCV001983820 benign not provided 2021-10-22 criteria provided, single submitter clinical testing

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