ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.308-377T>G

dbSNP: rs12668582
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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 RCV002089959 SCV002323321 benign Long QT syndrome 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713131 SCV005273309 benign not provided criteria provided, single submitter not provided

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