ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) (rs201207627)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000204961 SCV000262059 benign Primary ciliary dyskinesia 2020-10-30 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000252675 SCV000307605 likely benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000204961 SCV000468182 uncertain significance Primary ciliary dyskinesia 2016-06-14 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000252675 SCV000701188 benign not specified 2016-09-29 criteria provided, single submitter clinical testing
GeneDx RCV001577340 SCV001804697 likely benign not provided 2020-02-15 no assertion criteria provided clinical testing This variant is associated with the following publications: (PMID: 26302956)

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