ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.8797+20T>G

gnomAD frequency: 0.00217  dbSNP: rs16872911
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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 RCV000249397 SCV000307590 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001668472 SCV001889258 benign not provided 2021-05-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058027 SCV002370166 benign Primary ciliary dyskinesia 2025-02-01 criteria provided, single submitter clinical testing

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