ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.6274-13T>G (rs2965401)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000150438 SCV000197624 benign not specified 2013-02-21 criteria provided, single submitter clinical testing 6274-13T>G in intron 37 of DNAH11: This variant is not expected to have clinical significance because it has been identified in 22.0% (807/3666) of African Amer ican chromosomes from a broad population by the NHLBI Exome Sequencing Project ( http://evs.gs.washington.edu/EVS; dbSNP rs2965401).
PreventionGenetics,PreventionGenetics RCV000150438 SCV000307551 benign not specified 2016-03-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000400165 SCV000468126 benign Primary ciliary dyskinesia 2016-06-14 criteria provided, single submitter clinical testing

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