ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.3497A>C (p.His1166Pro)

gnomAD frequency: 0.00001  dbSNP: rs575476197
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000393983 SCV000468086 uncertain significance Primary ciliary dyskinesia 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000393983 SCV004617830 benign Primary ciliary dyskinesia 2023-07-07 criteria provided, single submitter clinical testing

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