ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.882+7A>G

gnomAD frequency: 0.00004  dbSNP: rs533700730
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000629594 SCV000750548 benign Primary ciliary dyskinesia 2024-01-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003437336 SCV004163773 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing DNAH11: BP4

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