ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1685+8C>T

gnomAD frequency: 0.00002  dbSNP: rs768101676
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001394367 SCV001596050 likely benign Long QT syndrome 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV001713141 SCV001943241 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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