ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.4378-17_4378-16insATTTA (rs57952953)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000079620 SCV000111503 benign not specified 2013-05-09 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000079620 SCV000307513 benign not specified criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000079620 SCV001744599 benign not specified no assertion criteria provided clinical testing

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