ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.5329-9T>C (rs773240082)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000253895 SCV000307531 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000866095 SCV001007145 likely benign not provided 2018-11-06 criteria provided, single submitter clinical testing
Invitae RCV001452378 SCV001656038 likely benign Primary ciliary dyskinesia 2018-11-06 criteria provided, single submitter clinical testing

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