ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.8155-19C>T

gnomAD frequency: 0.05613  dbSNP: rs729657
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243454 SCV000307583 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001696191 SCV001916113 benign not provided 2019-02-05 criteria provided, single submitter clinical testing
Invitae RCV002058026 SCV002408955 benign Primary ciliary dyskinesia 2024-02-01 criteria provided, single submitter clinical testing

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