ClinVar Miner

Submissions for variant NM_172362.3(KCNH1):c.80-7_80-6del

dbSNP: rs56223346
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001573400 SCV001901513 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573400 SCV001799226 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726591 SCV001965268 benign not specified no assertion criteria provided clinical testing

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