ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.-29GGCCCGCCC[1]

dbSNP: rs754605400
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001842819 SCV000234052 benign Cardiac arrhythmia 2014-08-23 criteria provided, single submitter clinical testing The variant is found in LQT panel(s).
Color Diagnostics, LLC DBA Color Health RCV001842819 SCV001350185 likely benign Cardiac arrhythmia 2018-06-26 criteria provided, single submitter clinical testing

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