ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.4377+20G>A

gnomAD frequency: 0.02672  dbSNP: rs113270736
Minimum review status: Collection method:
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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 RCV000246113 SCV000307512 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001675708 SCV001894262 benign not provided 2019-03-03 criteria provided, single submitter clinical testing
Invitae RCV002058018 SCV002402464 benign Primary ciliary dyskinesia 2024-01-31 criteria provided, single submitter clinical testing

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