ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.3261C>T (p.Gly1087=)

dbSNP: rs1584841732
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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 RCV000872193 SCV001013975 likely benign Long QT syndrome 2024-01-23 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001842544 SCV001341076 likely benign Cardiac arrhythmia 2019-07-26 criteria provided, single submitter clinical testing

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