ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.5924+19A>G

gnomAD frequency: 0.00361  dbSNP: rs112923391
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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 RCV000253964 SCV000307545 benign not specified criteria provided, single submitter clinical testing
Invitae RCV002058019 SCV002406604 benign Primary ciliary dyskinesia 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV002285290 SCV002575200 likely benign not provided 2020-02-25 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.

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