ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.12387+20T>A

gnomAD frequency: 0.01419  dbSNP: rs116529653
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000254403 SCV000307445 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001569060 SCV001793047 likely benign not provided 2018-12-31 criteria provided, single submitter clinical testing
Invitae RCV002058012 SCV002467578 benign Primary ciliary dyskinesia 2024-01-31 criteria provided, single submitter clinical testing

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